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Hurley
etal. Harm Reduction Journal (2023) 20:28
https://doi.org/10.1186/s12954-023-00760-7
RESEARCH
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Open Access
Harm Reduction Journal
Contraception use amongindividuals
withsubstance use disorder increases tenfold
withpatient-centered, mobile services:
aquasi-experimental study
Emily A. Hurley
1,2,3*
, Kathy Goggin
1,2,4
, Kimberly Piña‑Brugman
1
, Janelle R. Noel‑MacDonnell
1,2
, Andrea Allen
5
,
Sarah Finocchario‑Kessler
6
and Melissa K. Miller
2,7
Abstract
Background Individuals with substance use disorders (SUD) have disproportionately high rates of unintended
pregnancy. Reducing harm associated with this risk and its biopsychosocial consequences requires evidence‑based,
non‑coercive interventions that ensure access to contraception for individuals who choose to prevent pregnancy. We
examined feasibility and impact of SexHealth Mobile, a mobile unit‑based intervention that aimed to increase access
to patient‑centered contraceptive care for individuals in SUD recovery programs.
Methods We conducted a quasi‑experimental study (enhanced usual care [EUC] followed by intervention) at three
recovery centers with participants (n = 98) at risk for unintended pregnancy. EUC participants were offered printed
information on community locations where they could access contraception care. SexHealth Mobile participants
were offered same‑day, onsite clinical consultation on a medical mobile unit and contraception if desired. The primary
outcome was use of contraception (hormonal or intrauterine device) at one‑month post‑enrollment. Secondary out‑
comes were at two‑weeks and three‑months. Confidence in preventing unintended pregnancy, reasons for non‑use
of contraception at follow‑up, and intervention feasibility were also assessed.
Results Participants (median age = 31, range 19–40) enrolled in the intervention period were almost 10 times more
likely to be using contraception at one‑month (51.5%) versus the those enrolled in the EUC period (5.4%) (unadjusted
relative risk [URR] = 9.3 [95%CI: 2.3–37.1]; adjusted relative risk [ARR] = 9.8 [95%CI: 2.4–39.2]). Intervention participants
were also more likely to be using contraception at 2‑weeks (38.7% vs. 2.6%; URR = 14.3 [95%CI: 2.0–104.1]) and three‑
months (40.9% vs. 13.9%; URR = 2.9 [95% CI: 1.1–7.4]). EUC participants reported more barriers (cost, time) and less
confidence in preventing unintended pregnancies. Mixed‑methods feasibility data indicated high acceptability and
feasible integration into recovery settings.
Conclusions Mobile contraceptive care based on principles of reproductive justice and harm reduction reduces
access barriers, is feasible to implement in SUD recovery settings, and increases contraception use. Expanding
interventions like SexHealth Mobile may help reduce harm from unintended pregnancies among individuals in SUD
recovery.
*Correspondence:
Emily A. Hurley
Full list of author information is available at the end of the article
Page 2 of 11
Hurleyetal. Harm Reduction Journal (2023) 20:28
Trial Registration NCT04227145.
Keywords Contraception, Reproductive justice, Substance use disorders, Recovery, Sexual health, Mobile unit
Introduction
Ensuring access to contraception is critical for popula-
tions at high risk for unintended pregnancies, particu-
larly those in states with restricted abortion access.
Women with a history of substance use disorders
(SUD) have long suffered disproportionately high rates
of unintended pregnancies. A nationally representative
sample of women reported a 70% increased likelihood
of unintended pregnancy among women with precon
-
ception illicit or recreational drug use, compared to
those with no drug use [1]. In a study of women with
opioid use disorder, nine in ten pregnancies were unin
-
tended, a rate two to three times higher than in the
general population [2]. Over the last two decades, the
proportion of pregnant women reporting non-pre
-
scription opioid use has quadrupled and the proportion
reporting methamphetamine use has doubled [3, 4].
Further, overall SUD rates have risen in the U.S. since
the onset of the COVID-19 pandemic [5].
Women with history of SUD often desire contracep
-
tion but face accessbarriers [69]. ey report cost,
insurance and/or transportation challenges, and are
overallless likely to have regular contact with primary
or reproductive health carethan women without SUD
[8, 10]. Women with SUD may also avoid contracep
-
tion care-seeking due to experienced or anticipated
stigma from providers [6, 8, 9, 11]. Further, theyoften
lack accurate information about contraception options
[7, 8] or may not prioritize seeking contraception
when actively trying to obtain substances [8]. Address
-
ing these barriers can help individuals with SUD gain
more control over when and if they become pregnant,
and avoid the often devastating health and psychosocial
consequences associated with unintended pregnancies
(e.g., losing childcustody) [1215].
Entry into recovery services is an opportune time
to help individuals meet unmet contraception desires.
While contraception access is important at all stages of
SUD including recovery, women describe recovery ini
-
tiation as a time of peak readiness to address broader
health needs. Further, women initiating recovery gen
-
erally state they prefer to plan pregnancies for a time
when they have reached stable, long-term recovery [8,
16, 17]. Meeting contraception desires with long-acting
reversible contraception (LARC) early in recovery can
also provide longer-term protection for the 40–60% of
women who return to use within one year of beginning
treatment [18].
Although some studies have shown increased contra
-
ceptive use with SUD recovery-based interventions, they
have had limitations [19]. Few interventions have fully
demonstrated commitment to principals of reproductive
justice (the right to maintain bodily autonomy, includ
-
ing choice over reproduction) and harm reduction (the
right to access services that reduce harmful effects of
substance use without judgement or pressure to change
behavior) [8, 9, 20]. Some have included the controversial
use of incentives or directive behavior change goals to
encourage contraception use [21, 22]. Further, many have
not been able to provide LARC and have offered only
limited options [23]. Our formative research suggested
women would find contraception services valuable and
make use of them without incentives, given that the ser
-
vices: (1) maximize access to the full range of contracep-
tion options, (2) provide contraception free or at minimal
cost, (3) offer non-judgmental, non-coercive patient-cen
-
tered care, (4) are delivered by qualified, trusted provid-
ers, and (5) are supported and promoted by their peers
[9].
We designed an intervention, SexHealth Mobile, to
meet these community-derived priorities for people with
SUD at risk of unintended pregnancy. SexHealth Mobile
featured a medical mobile unit (MMU) equipped with a
range of free contraception options and a reproductive
health care provider who offered counseling and pre
-
scriptions. e intervention also trained outreach leaders
at recovery centers to support free choice and provid
-
ing accurate, non-coercive information on contracep-
tion options. is pilot study examines the feasibility of
SexHealth Mobile and its impact on contraception use
among woman in SUD recovery programs in Kansas City,
Missouri.
Methods
We conducted a quasi-experimental study with an inter-
rupted time series design (i.e., enhanced usual care [EUC]
followed by intervention). We compared contraception
use one-month after enrollment among participants
enrolled in the two different time periods. e study was
approved by e Institutional Review Board at Childrens
Mercy Kansas City.
Setting andparticipants
SexHealth Mobile was implemented in partnership with
a federally qualified health center (FHQC) in Kansas
City that was already operating a MMU to provide basic
Page 3 of 11
Hurleyetal. Harm Reduction Journal (2023) 20:28
health services at community locations with high need,
including recovery centers. For this study, we selected
three recovery centers that already partnered with the
FHQC to receive periodic MMU visits for basic health
services (e.g., seasonal vaccination, basic screenings, and
treatment of non-emergency illness and injuries). e
three recovery centers were providing services for clients
with any type of SUD, most commonly polysubstance use
disorders that included use of methamphetamines and/
or opioids. Two centers were residential, serving indi
-
viduals who had initiated recovery and were expected to
not be using substances other than tobacco while in the
program. e other was outpatient, serving individuals at
various stages of recovery and active substance use. Prior
to our intervention, the FHQC provided contraception
and reproductive health services (free or discounted) at
their main center, but not yet on the MMU.. Recovery
centers did not routinely screen for reproductive health
needs but would informally recommend community clin
-
ics (including the FHQC partner) for individuals inter-
ested in services.
Recovery center clients were eligible if they were: (1)
aged 18–40; (2) screened positive for a lifetime history
of problematic drinking or drug use according to CAGE-
AID tool [24]; (3) able to become pregnant (assigned
female sex at birth, pre-menopausal, not sterilized or
diagnosed with infertility) but not currently pregnant; (4)
not currently using an intrauterine device or hormonal
contraception (i.e., oral contraceptive pill, transdermal
patch, vaginal ring, injectable, subdermal implant); and
(5) not previously enrolled in either phase of the study.
Procedures
Study staff worked with recovery centers to share infor-
mation about the study and visited each site periodically
for eligibility screening and enrollment. Interested clients
were screened individually by study staff and those eligi
-
ble provided written informed consent. Site visits con-
tinued until the sample size target for each time period
(n = 46) was reached or exceeded.
All participants completed a 15-min baseline question
-
naire via REDCap that included demographic, substance
use, and reproductive health history. For the EUC period
(Aug–Nov. 2020), we created a printed information sheet
that listed community locations where each recovery
center would typically recommend clients contact to
access contraception care. By formalizing this contact
sheet and offering it to women after the baseline ques
-
tionnaire on reproductive health needs, we “enhanced”
recovery centers’ usual care procedures for reproduc
-
tive health. In the SexHealth Mobile intervention period
(April-Sept. 2021), participants were offered the oppor
-
tunity to see a reproductive health care provider on the
MMU and, if desired, obtain contraception on-site. Inter
-
vention period participants not interested in MMU visits
were also offered EUC printed information sheets. Par
-
ticipants in both time periods completed a 5-min post-
intervention survey as well as 2-week, 1-month, and
3-month follow-up phone assessments. Participants were
compensated $20 for completion of the baseline/post-
intervention survey, $15 each for 2-week and 1-month
follow-ups, and $20 for the 3-month follow-up.
SexHealth mobile intervention
SexHealth Mobile is grounded in formative research
and centered on reproductive justice and harm reduc
-
tion principles. e intervention featured “SexHealth
Mobile Days” where the MMU, clinical staff, and study
staff would visit each recovery center. In preparation,
we worked with the FHQC leadership and clinical staff
to integrate contraceptive services within the MMU.
is included one nurse practitioner with experience in
patient-centered contraception care for SUD patients,
one care assistant, and materials required for on-site pro
-
vision of contraceptive medications (e.g., pregnancy tests,
needles, syringes). e nurse practitioner (author AA)
specialized in women’s health, independently placed con
-
traceptive devices, and hadworked at the partner FHQC
for seven years (including previously providing general
health care on the MMU). We worked with recovery
centers and FHQC staff to ensure services were provided
in a way that was acceptable to potential patients, includ
-
ing arranging for pregnancy testing with urine collected
by patients themselves within recovery center facilities.
On SexHealth Mobile Days, the provider offered con
-
traceptive options on the MMU free of charge, includ-
ing hormonal (i.e., pills, transdermal patch, vaginal
ring, injection, subdermal implant) and non-hormonal
(diaphragm, condoms). Participants who chose short-
term hormonal contraception (pills, patch, ring, injec
-
tion) were given dosage for three months of pregnancy
prevention and instructions for refills/follow-up at the
main FQHC. e MMU was not outfitted with a stand
-
ard patient exam table that could be used for gynecologi-
cal procedures, thus we could not offer same-day IUDs.
However, participants interested in IUDs could speak
to the provider on the MMU, schedule a facility-based
IUD insertion appointment at the main FHQC with the
same provider, and obtain a bridging method to protect
against pregnancy until IUD insertion. Further, partici
-
pants interested in sexual and reproductive health ser-
vices beyond contraception were also able to speak with
the MMU provider and schedule appropriate facility-
based FHQC appointments. Study staff also offered free
condoms and home pregnancy tests at the enrollment
table for anyone at the recovery center. We conducted
Page 4 of 11
Hurleyetal. Harm Reduction Journal (2023) 20:28
ten SexHealth Mobile Days before reaching our target
recruitment in intervention period, with four visits at the
larger residential center, two at the smaller residential
center, and four at the outpatient center.
At each recovery center, 2–4 individuals who already
occupied formal roles as trusted resources for clients (7
peer mentors, 3 social workers) were trained as “outreach
leaders” to promote SexHealth Mobile Days and organ
-
ize interested clients. Training covered basic principles
of reproductive justice and harm reduction, contracep
-
tion options, needs and challenges faced by individuals
with SUD in preventing unintended pregnancies, and
strategies for using client-centered and trauma-informed
approaches when talking about contraception.
Outreach leaders and study staff stressed that all activi
-
ties on SexHealth Mobile Days were completely volun-
tary, and people could obtain a clinic referral or meet
with MMU providers and receive free contraception even
if they chose not to enroll in the study, or were not eli
-
gible due to previous enrollment in the EUC period or
other ineligibility criteria. Individuals could also enroll
in the study and meet with MMU providers even if they
were unsure or not interested in taking up contraception.
Outcome measures
Feasibility
We assessed feasibility of SexHealth Mobile according
to selected Bowen feasibility constructs [25]. Table 1
lists and defines constructs and measures of assessment,
including participant survey items and study staff field
notes.
Primary andsecondary outcomes
e primary outcome was use of IUD or hormonal
contraception (pills, patch, ring, contraception injec
-
tion, subdermal implant) at one-month post-enroll-
ment. Secondary outcomes were use at two-weeks and
three-months. We also explored group differences in
confidence in preventing unintended pregnancy at post-
intervention and as a change from baseline to post-inter
-
vention (reported on a repeated 5-point scale ranging
from “not at all confident” to “extremely confident”) as
well as reasons for non-use at one-month (including rea
-
sons for not attending clinic visits, picking up prescrip-
tions, and/or starting birth control).
Data analysis
Descriptive analysis was carried out for all variables, with
comparisons made between groups with Chi-Square or
Fisher’s Exact tests for categorical variables as appro
-
priate based on cell values, and two-sided independent
t-test for continuous variables. We compared groups
as intention-to-treat on the primary and secondary
outcomes using Fisher’s Exact test and Poisson regression
with robust standard errors (unadjusted and adjusted).
e adjusted model included demographic factors
known to influence contraception use or identified as
having influence through a series of bivariate associations
with contraception use, including recovery site (residen
-
tial vs. outpatient), pregnancy intention (trying to avoid/
wouldn’t mind avoiding vs. other), pregnancy history
(ever been pregnant vs. not) and recency of substance
use (defined as use within the three months prior to base
-
line vs. none). We analyzed the primary outcome again
including participants who had missed the one-month
assessment but reported a contraception injection (which
protects for three months) at post-intervention or two
weeks. Quantitative analyses were completed in SAS Ver
-
sion 9.4. (SAS Institute, Cary, NC). Field notes were ana-
lyzed with qualitative coding to identify facilitators and
barriers according to Bowen’s feasibility constructs [25].
Results
Baseline demographics
We enrolled 98 participants (48 in EUC period, 50 in
intervention period). An additional 17 were ineligi
-
ble after screening (Fig.1). Follow-ups were completed
by 70.4% at two-weeks (79.2% EUC, 62.0% interven
-
tion), 71.4% at one-month (77.1% EUC, 66.0% interven-
tion), and 59.2% at three-months (75.0% EUC, 44.0%
intervention). At baseline, participants in both groups
were similar in age (median = 31, range 19–40), ethnic
-
ity (92.9% non-Hispanic), educational status (76.5% high
school graduate or higher) and marital status (69.4% sin
-
gle/never married) (Table 2). Most identified as white
(79.6%) with more identifying as Black/African American
in EUC (12.5%) versus intervention periods (4.0%). One
participant (in the intervention period) identified as male
and all others identified as female. Almost half (46.9%)
were uninsured while most others had public insurance
(35.7%).
EUC and intervention participants were also similar
in substance use and sexual/reproductive health his
-
tory (p-values > 0.05 unless otherwise noted). Partici-
pants were receiving recoveryservices at the outpatient
(48.0%) or one of two residential (52.0%) centers. Most
participants had used substances other than tobacco
within the past three months, with a greater propor
-
tion of EUC participants reporting recent substance use
compared to intervention participants (85.4%, 66.0%;
p = 0.026). e majority had used amphetamines (78.6%),
cannabis (80.6%), alcohol (76.5%), opioids (59.2%), and/
or cocaine (60.2%) at some point in their life. Most had
a history of polysubstance use (i.e., use of two or more
substances other than tobacco), with slightly more of the
EUC (58.3%) than the intervention group (42.0%). Most
Page 5 of 11
Hurleyetal. Harm Reduction Journal (2023) 20:28
Table 1 Assessment of SexHealth Mobile feasibility: constructs, indicators, and measures
1
Intervention participants only;
2
Intervention participants completing MMU visits only;
3
Intervention participants who reported interactions with Outreach Leaders only;
4
Enhanced usual care participants only
Feasibility Construct [25] Indicator Measure
Demand
(To what extent is the intervention likely to be used?)
Proportion of intervention participants interested in an MMU
visit on a SexHealth Mobile Day
Baseline survey item
1
Proportion of intervention participants completing MMU visits
who received on‑site contraception
Post‑intervention survey item
2
Number of additional MMU visits among individuals not eligible
for the study (e.g., not within age range, participated in EUC
period, already using contraception but interested in other
methods)
Study staff field notes
Number of individuals (participants and non‑participants) who
took free condoms and pregnancy tests; number of study par‑
ticipants reporting taking free condoms at MMU visit
Study staff field notes; post‑intervention survey
1
Acceptability
(How do stakeholders react to the intervention?)
Intervention participants’ ratings of post‑MMU visit satisfaction
and likelihood of recommending to a friend
Post‑intervention survey items
2
Overall satisfaction: (4‑point scale; range: “not satisfied at all” to
“very satisfied”)
Likelihood of recommending MMU (5‑point scale from extremely
unlikely to extremely likely”)
Intervention participants’ ratings of patient‑centeredness of
MMU provider
Post‑intervention survey items
2
Person-Centered Contraceptive Counseling Survey (PCCCS) [26]: using
“top score (an excellent” rating on all four items)
Intervention participants’ ratings of outreach leader support Baseline survey item
3
Level of agreement that outreach leader supported them in mak‑
ing their own decision (4‑point from “strongly disagree to strongly
agree)
Recovery center leadership support and cooperation in facilitat‑
ing implementation
Study staff field notes
Proportion of EUC participants who reported they would have
used the MMU if it had been available
Post‑intervention survey item
4
Implementation
(To what extent can the intervention be implemented as planned?)
Outreach leader activity in intervention period Study staff field notes
Intervention participants’ self‑reported interactions with out‑
reach leaders
Baseline survey item
1
Acceptability of patient flow, volume, and wait time for all
stakeholders
Study staff field notes
Ability of MMU/provider to meet needs of patients Study staff field notes
Integration
(To what extent can the intervention be integrated within an exist-
ing system?)
Overall successes and challenges of integrating recovery and
FHQC service systems, including personnel collaboration,
scheduling, and facilitating pre‑MMU patient procedures (e.g.,
paperwork, urine samples, implant insertion)
Study staff field notes
Page 6 of 11
Hurleyetal. Harm Reduction Journal (2023) 20:28
(72.4%) indicated they had received some medical care in
the past 12months and 58.2% said there was a time in the
past 12months they thought they should have accessed
health care but did not.
Most had no (43.9%) or one (44.9%) current male sexual
partner with few reporting they were trying to get preg
-
nant (2.0%). At last vaginal sex, most reported no preg-
nancy prevention method (48.0%) or withdrawal (24.5%).
Four-fifths had not used a condom at last sex. e major
-
ity had lifetime experience with contraception, most
commonly the pill (67.3%) and condoms (67.3%). Most
had experienced pregnancy (80.6%) and two reported
previous abortion. Most (72.4%) had at least one living
child and of those with children, and 60.5% reported their
child/children living in foster care or with someone else
at some point.
Intervention feasibility
Table3 summarizes mixed-methods feasibility findings.
Overall intervention demand was high, as 43 interven
-
tion participants (86.0%) requested an MMU visit for
contraception counseling. Of the 39 who completed a
visit and post-intervention survey, 22 (56.4%) reported
receiving a form of hormonal contraception on the
Fig. 1 Screening, enrollment, & follow‑up of participants in SexHealth Mobile Intervention
Page 7 of 11
Hurleyetal. Harm Reduction Journal (2023) 20:28
MMU (pills=14, contraception injection=5, subder-
mal implant=1, patches=1,rings=1). Additionally,
two participants (5.1%) were prescribed a diaphragm
and 18 (46.2%) took condoms Acceptability was high, as
most intervention participants who visited the MMU
were “very satisfied” with their visit (92.3%) and gave the
provider a top score for person-centeredness (86.8%).
Observations and field notes indicated successful imple
-
mentation and integration of services, with minor chal-
lenges (detailed in Table3).
Contraception use
For our primary outcome, 51.5% (17/33) of participants
in the intervention period were using contraception at
one-month post-baseline compared to 5.4% (2/37) in the
EUC period (Fishers exact test p = 0.001) (unadjusted
relative risk (URR) = 9.3 [95%CI: 2.3–37.1]; p = 0.0016).
Both EUC participants reported contraception injection,
while intervention participants reported pills (n = 11),
contraception injections (n = 3), implant (n = 1), patch
(n = 1) and ring (n = 1). e proportion of interven
-
tion participants using contraception was also higher
than that in EUC at 2-weeks (38.7% [12/31] vs. 2.6%
[1/38]; p = < 0.0001) (URR = 14.3 [95% CI: 2.0–104.1];
p = 0.0085) and three months (40.9% [9/22] vs. 13.9%
[5/36]; p = 0.020) (URR = 2.9 [95%CI: 1.1–7.4]; p = 0.031).
Likelihood of contraception use at one-month
remained high after adjusting for age, recovery center
type, pregnancy intention, pregnancy history, and
substance use at three-months (adjusted relative risk
(ARR) = 9.8 [95%CI: 2.4–39.2]; p = 0.0013). One addi
-
tional participant could be assumed to be using con-
traception at one-month despite not completing the
assessment, as she reported receiving a contraception
injection on the post-intervention survey, strengthen
-
ing the relative risk in the unadjusted (RR = 9.7 [95%CI:
2.5–39.1]; p = 0.0012) and adjusted models (ARR = 10.0
[95%CI: 2.5–40.0]; p = 0.0012).
Table 2 Demographics (including substance use, sexual/repro health history)
*
Where options do not add to 100%, one or more participants marked “prefer not to answer”
Enhanced Usual Care (EUC)
(n = 48)
SexHealth Mobile Intervention
(n = 50)
p-value
Age in years (Median, [IQR]) 30 (25, 34) 32.5 (28, 35) 0.143
Race (n, %) 0.065
American Indian/Alaska Native 1 (2.1%) 1 (2.0%)
Asian 0 (0.0%) 1 (2.0%)
Black/ African American 6 (12.5%) 2 (4.0%)
White 40 (83.3%) 38 (76.0%)
Other 1 (2.1%) 7 (14.0%)
Ethnicity 1.000
Non‑Hispanic 45 (93.8%) 46 (92.0%)
Hispanic/ Latina 3 (6.3%) 3 (6.0%)
Educational Level 0.110
Less than High School 10 (20.8%) 13 (26.0%)
High school graduate or GED 22 (45.8%) 24 (48.0%)
Post‑high school training/ some college 15 (31.1%) 9 (18.0%)
Undergraduate degree or Higher 1 (2.1%) 4 (8.0%)
Marital status 0.714
Single (never married) 34 (70.8%) 34 (68.0%)
Separated/ Divorced 11 (22.9%) 11 (22.0%)
Married/ domestic partnership 2 (4.2%) 3 (6.0%)
Widowed 1 (2.1%) 2 (4.0%)
Health Insurance Status 0.632
Private 2 (4.2%) 5 (10.0%)
Public (Medicare, Medicaid) 16 (33.3%) 19 (38.0%)
Other 3 (6.3%) 4 (8.0%)
Uninsured 26 (54.2%) 20 (40.0%)
Page 8 of 11
Hurleyetal. Harm Reduction Journal (2023) 20:28
Condence andbarriers
Self-reported confidence in one’s own ability to protect
against unwanted pregnancy (dichotomized as “very/
extremely confident” and “not confident/low confident/
not sure”) was more prevalent in the intervention than
the EUC group in the post-intervention survey (90% vs.
70%; p = < 0.0001). A greater proportion of participants
increased from “not confident/low confident/not sure”
at baseline to “very confident/extremely confident” post-
interventionin the intervention (28.0% )versus the EUC
group (12.5%; p = < 0.001).
e most frequently cited reason for non-use of contra
-
ception at one-month among both groups was “decided
did not want/need birth control” (EUC = 27.1%; inter
-
vention = 16.0%; p = 0.18). Some participants offered
additional explanation for not being interested in contra
-
ception, including not being sexually active or not having
male partners. A few also expressed ambivalence toward
becomingpregnant. e barrier“not enough time” (to
complete referral appointment, pick up prescription,
and/or start method) was reported more frequently in the
EUC group (22.9%) than the intervention group (6.0%;
p = 0.001). “Insurance/cost” barriers were also reported
Table 3 SexHealth Mobile feasibility: Key findings
1
Full description of each construct’s operationalization and measurement is available in Table1
Feasibility Construct
1
Facilitators ( +) and Barriers (-)
Demand (To what extent is the intervention likely to be used?) 86% of intervention participants indicated interest in an MMU visit on a
SexHealth Mobile Day ( +)
56.4% of intervention participants who visited the MMU received on‑site
contraception ( +)
21 individuals not enrolled in the study had an MMU visit ( +)
42 individuals took free condoms and 30 took free pregnancy tests from
study staff; 18 study participants took free condoms at an MMU visit ( +)
Acceptability (How do stakeholders react to the intervention?) 92.3% of intervention participants who visited the MMU were “very satis‑
fied” with their visit; 97.4% were “likely or extremely likely” to recommend
to a friend (+)
86.8% of intervention participants who visited the MMU gave the provider
a top score for patient‑centeredness ( +)
76.6% of intervention participants who spoke to an outreach leader
agreed” or strongly agreed” that the leader supported them in making
their own decisions ( +)
Recovery center leadership actively supported implementation at all three
sites ( +)
81.3% of EUC participants reported they would have used the MMU if it
had been available ( +)
Implementation (To what extent can the intervention be implemented as
planned?)
Outreach leaders successfully mobilized attendance for SexHealth Mobile
Days ( +)
60.0% of intervention participants reported having spoken to an outreach
leader about SexHealth Mobile ( +)
Patients with sexual or reproductive health needs beyond available con‑
traception methods were able to have a preliminary consultation on the
MMU and schedule a later appointment at the main FQHC ( +)
Interest in MMU appointments (which were often lengthy) sometimes
exceeded the number of interested individuals (‑)
Some women were asked to wait for a future confirmatory negative preg‑
nancy test before receiving a subdermal implant (‑)
Integration (To what extent can the intervention be integrated within an
existing system?)
Pre‑existing FQHC/recovery center relationships facilitated smooth service
integration and service provision for patients regardless of insurance status
( +)
MMU process were easily adapted to accommodate contraception care
(including implant insertion and self‑collection of urine) and SexHealth
Mobile Days were easily integrated into recovery center activities ( +)
Limited availability of the FQHC MMU and staff created scheduling chal‑
lenges ( +)
Patients not yet registered to receive services with the FQHC faced a high
burden of paperwork (‑)
Page 9 of 11
Hurleyetal. Harm Reduction Journal (2023) 20:28
more frequently in the EUC (14.6%) versus interven-
tion (2.1%; p = 0.023). Less frequently cited barriers
were “transportation” (EUC = 6.3%; intervention = 2.0%,
p = 0.288) and “COVID-19-related” (EUC = 2.1%; inter
-
vention = 0%, p = 0.305).
Discussion
Participants offered free, autonomy-supportive, mobile
contraceptive services at SUD recovery centers were
over nine times more likely to be using contraception
at one-month post baseline than those exposed to EUC
(51.5% vs. 5.4%). e estimated advantage of the inter
-
vention over EUC strengthens to tenfold when control-
ling for age, recovery center type, pregnancy intention,
pregnancy history, substance use within three months
of the study and assuming continual protection for the
one lost-to-follow-up participant who received a contra
-
ception injection during her visit. Participants exposed
to the intervention and not using contraception at one-
month typically reported that this was their preference
(they decided they did not want or did not need contra
-
ception) indicating that this was not a limit of the inter-
vention, but rather a personal choice. Among those not
using contraception at one-month, EUC participants
reported significantly more barriers in terms of time
and cost than intervention participants. Participants
exposed to SexHealth Mobile also reported higher post-
intervention confidence in their ability to protect against
unwanted pregnancy.
Our intervention was designed to address key limi
-
tations of past interventions aimed at increasing con-
traception access for individuals with SUD. Based on
formative research with our target community (inter
-
views, focus groups) [9], we carefully designed all aspects
of the intervention to stress reproductive justice (e.g.,
outreach leader role/training stressed a non-coercive
approach, participation/enrollment for all regardless of
contraceptive interest, and provision of all contracep
-
tion options that could be accommodated on the MMU
free of charge). Prior contraception access interven
-
tions for individuals with SUD have included behavioral
strategies or incentives [19] and some have drawn con
-
cern about the potential for coercion from providers
[21, 22]. oughtful recent adaptions have linked finan
-
cial incentives to attendance at contraception appoint-
ments instead of to contraception use directly [27, 28],
but thisstrategy was viewed as unnecessary and poten
-
tially problematic by our community partners. SexHealth
Mobile was highly successful in increasing contracep
-
tion use without the use of incentives. It also offered
a sustainable intervention model by building off an
existing FQHC and its trusted partnerships with local
recovery centers. Our work also confirms feasibility of
administering longer-acting contraception (injections
and subdermal implant) via MMU in a U.S. urban setting
[29, 30]. ough MMU-based IUD insertion is possible,
[31] it was not feasible to offer through our intervention,
and more research is needed to determine how to best
integrate IUD provision into scalable MMU programs.
Finally, while MMUs have shown high reach and uptake
for contraception in low and middle-income countries,
their use to among at-risk populations in the U.S. has
not been extensively evaluated [31, 32]. Ours study is the
first to estimate the impact of MMU-based contraception
care compared to EUC.
SexHealth Mobile demonstrated high demand and
acceptability, with strengths and limitations in its imple
-
mentation and integration with existing services. e
vast majority of intervention participants made use of
the MMU, with high ratings of overall satisfaction and
person-centeredness of the provider. Many interven
-
tion participants chose contraception (56.4%), but others
reported they decided they did not want or did not need
contraception, a strong indicator that they felt reproduc
-
tive autonomy, and were not coerced toward contracep-
tion even if they elected to visit the MMU. Given our
formative research findings that LARCs would be highly
desirable option, the low uptake of subdermal implants
on the MMU was surprising. On SexHealth Mobile Days,
many participants were still hesitant or unfamiliar with
subdermal implants and not ready to commit to the pro
-
cedure. is may have been because many participants
took advantage of MMU visits who had not been reached
by education efforts leading up to SexHealth Mobile
Days (40% reported not having prior conversations about
contraception with an outreach leader) and thus may
not have had adequate time to thoroughly consider new
methods. Many expressed interest interested in learning
about new methods like implants and considering them
for a later date, but on a day-of, walk-in MMU service,
were ultimately most comfortable obtaining familiar
methods (e.g., pills). Another key barrier to implementa
-
tion was that some participants were told to wait several
weeks to conduct another pregnancy test before getting
a subdermal implant (a standard practice at this FHQC
but inconsistent with evidence-based guidelines) [33]
and were given a bridge method until a later visit. Fur
-
ther, challenges in scheduling the MMU and paperwork
for new patients sometimes limited the number of MMU
visits offered within on SexHealth Mobile Day.
Limitations
In this quasi-experimental design, participants were
not randomized to conditions. e similarities in both
groups on demographic factors proximally associ
-
ated with contraception use, and the fact that all were
Page 10 of 11
Hurleyetal. Harm Reduction Journal (2023) 20:28
recruited from the same sites, however, minimizes the
possibility that differences observed between interven
-
tion/EUC conditions could be attributed to baseline
participant characteristics. e EUC and intervention
periods also occurred at different time points, thus
there may have been inherent benefits to the inter
-
vention period occurring later (e.g., more exposure at
each site to sexual health information/activities related
to the study). We do not believe that the trajectory of
the COVID-19 pandemic had a significant impact on
results, as we did not initiate enrollment in the EUC
period until in-person activities at recovery centers and
referral health centers had resumed. In reporting bar
-
riers to contraception, just one participant in the EUC
period named a COVID-19 related factor. We alsonote
limitations in diversity in our sample as the majority of
our sample identified as white and non-Hispanic.
Conclusion
SexHealth Mobile expanded access to patient-centered
contraception options for individuals with SUD, demon
-
strating meaningful increases in contraception coverage
and confidence to protect against unintended pregnancy,
without the need for incentives or persuasion. Alleviating
barriers to contraception by expanding interventions like
SexHealth Mobile could help empower more individuals
entering substance use recovery to prevent unintended
pregnancy. More research is needed to adapt and imple
-
ment similar interventions for individuals with SUD who
are not connected to traditional recovery centers.
Acknowledgements
The authors would like to thank all the implementing partners that made this
project possible, especially Rachel Melson, Jennifer Frost, Lori Glenski, Angel
Modersohn, DeAnte Hurd, Amanda Derington, Sarah Knopf‑Amelung, Olivia
Deeken, Mollee Flores, Renee Harris, Erin Hestand, Kelli Hubbard, Bobbi Jo
Reed, Jesse Ibarra, Alex Irvin, Brenda Peters, and Alyssa Ibarra. We would also
like to thank Beth Canipe and Evelyn Donis de Miranda for help with data
collection and manuscript preparation, and all the participants who gave their
time and opinions.
Author contributions
Concept and design: EAH, KG, SFK and MKM. Acquisition, analysis, and/or
interpretation of data: All authors. Drafting of the manuscript: EAH. Critical
revision of the manuscript for important intellectual content: All authors.
Statistical analysis: JNM. Obtained funding: EAH, KG, MKM, SFK. Administrative
and technical support: KPB, AA. Supervision: EAH, MKM. All authors read and
approved the final manuscript.
Funding
Research reported in this work was supported by Organon & Co. The content
is solely the responsibility of the authors and does not necessarily represent
the views of Organon & Co. The funding source had no role in the design and
conduct of the study; collection, management, analysis, or interpretation of
the data; preparation, review, or approval of the manuscript.
Availability of data and materials
The datasets used during the current study are available from the correspond‑
ing author on reasonable request.
Declarations
Ethics approval and consent to participate
All participants provided written, informed consent prior to enrollment. The
study protocol was approved by the Institutional Review Board at Childrens
Mercy Kansas City (#1099).
Consent for publication
Not applicable.
Competing interests
EAH and MKM received investigator‑initiated grants from Organon & Co for
studies on contraception access. All other authors declare no competing
interests.
Author details
1
Division of Health Services and Outcomes Research, Childrens Mercy Kansas
City, 2401 Gillham Rd., Kansas City, MO 64108, USA.
2
Department of Pediat‑
rics, University of Missouri‑Kansas City School of Medicine, Kansas City, MO,
USA.
3
Department of Population Health, University of Kansas Medical Center,
Kansas City, KS, USA.
4
University of Missouri ‑ Kansas City School of Pharmacy,
Kansas City, MO, USA.
5
Swope Health Services, Kansas City, MO, USA.
6
Depart
ment of Family Medicine, University of Kansas Medical Center, Kansas City, KS,
USA.
7
Division of Emergency Medicine, Childrens Mercy Kansas City, Kansas
City, MO, USA.
Received: 28 October 2022 Accepted: 24 February 2023
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