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PLOS ONE logoLink to PLOS ONE
. 2021 Sep 29;16(9):e0257769. doi: 10.1371/journal.pone.0257769

Factors affecting uptake of the levonorgestrel-releasing intrauterine device: A mixed-method study of social franchise clients in Nigeria

Aurélie Brunie 1, Anthony Adindu Nwala 2, Kayla Stankevitz 3, Megan Lydon 3, Kendal Danna 4, Kayode Afolabi 5, Kate H Rademacher 3,*
Editor: Federico Ferrari6
PMCID: PMC8480829  PMID: 34587200

Abstract

Background

Despite the positive characteristics of the levonorgestrel-releasing intrauterine device (IUD)–a long-acting, highly effective contraceptive with important non-contraceptive attributes–the method has not been widely available in low- and middle-income countries. This study of hormonal IUD, copper IUD, implant and injectable users in Nigeria compares their characteristics, reasons for method choice, and experiences obtaining their method.

Methods

We conducted a phone survey with 888 women who received a hormonal IUD, copper IUD, contraceptive implant or injectable from 40 social franchise clinics across 18 states in Nigeria. We analyzed survey data descriptively by method and assessed factors associated with hormonal IUD use through multivariate logistic regression models. Follow-up in-depth interviews conducted with 32 women were analyzed thematically.

Results

There were few differences by method used in the socio-demographic profiles and contraceptive history of participants. Among users choosing a long-acting, reversible method, the top reasons for method choice included perceptions that the method was “right for my body,” long duration, recommended by provider, recommended by friends/family, few or manageable side effects, and high effectiveness. Among hormonal IUD users, 17% mentioned reduced bleeding (inclusive of lighter, shorter, or no period), and 16% mentioned treatment of heavy or painful periods. Qualitative data supported these findings. Among survey respondents, between 25% and 33% said they would have chosen no method if the method they received had not been available. Both quantitative and qualitative data indicated that partner support can affect contraceptive use, with in-depth interviews revealing that women typically needed partner permission to use contraception, but men were less influential in method choice.

Conclusions

Expanding access to the hormonal IUD as part of a full method mix provides an opportunity to expand contraceptive choice for women in Nigeria. Findings are timely as the government is poised to introduce the method on a wider scale.

Introduction

The levonorgestrel intrauterine device (IUD)–also known as the hormonal IUD–is a highly efficacious, long-acting contraceptive. The slow and steady localized release of progestin can minimize systemic side effects, and method use is associated with reduced menstrual blood loss and cramps. The hormonal IUD is a proven treatment for menorrhagia and uterine fibroids and potentially for anemia [15]. Yet availability of this method in low- and middle-income countries (LMIC) has previously been limited to small scale distribution in the commercial sector due to the high retail price of existing products. However, the landscape is changing, with more affordable products becoming available [6].

Historically, the prevalence of the copper IUD has been low in many countries in sub-Saharan Africa due to both supply- and demand-side barriers [7], and it is unclear to what degree uptake of the hormonal IUD would face the same challenges given that the two methods share some attributes (e.g., vaginal insertion) but also have key differences (e.g., different bleeding and side effect profiles) [8]. Available research on women’s perspectives on the hormonal IUD shows promise for introduction and acceptability of this method in sub-Saharan Africa. A study in a Kenyan clinic where postpartum women were offered the choice between condoms, lactational amenorrhea, pills, injectables, implants, the copper IUD and the hormonal IUD showed robust interest in the hormonal IUD, with 16% of participants opting for this method [9]. Qualitative interviews with hormonal IUD users in Ghana, Kenya and Nigeria all revealed favorable perceptions of the hormonal IUD among women [1012]. In Ghana, four in five hormonal IUD users recruited from six health facilities expressed satisfaction with the product [10]. Clients of mobile outreach teams, social franchise clinics and public sector facilities supported by Marie Stopes International in Nigeria who were interviewed three months after uptake all intended to continue the method, noting non-contraceptive benefits and fewer side effects compared with other methods [11]. Almost all current or recent hormonal IUD users from two Kenyan clinics reported positive experiences with the method, citing attributes including convenience, few side effects, method duration and reduced periods [12].

Monitoring data from several pilot introduction programs in Kenya, Nigeria, Madagascar, and Zambia indicate that the hormonal IUD is not simply a substitute for other long-acting reversible contraceptives (LARCs), including the copper IUD and implants. While between 25–65% of hormonal IUD acceptors surveyed in these programs told their provider they would have chosen another LARC if the hormonal IUD had not been available, 14–59% would have chosen a short-acting method, and between 3–30% said they would have left with no method. Across most programs, the most common reasons for choosing the hormonal IUD were its effectiveness, long-acting duration, and minimal side effects [13].

To date, little information is available about the user population for the hormonal IUD, what method attributes they find attractive and reasons for selecting the method; existing data are limited to special populations, qualitative interviews, and service statistics. The research presented in this paper is part of a prospective cohort study with LARC users intended to measure continuation rates. This paper describes the mixed-methods, baseline component of the study to expand the evidence base by providing additional insight into the factors affecting uptake of the method. Objectives specific to the baseline component of the study were to compare women choosing the hormonal IUD to women choosing other methods (copper IUD, implant, and three-month injectable) in terms of their characteristics, reasons for method choice, and experiences obtaining their method.

Materials and methods

Study setting

In 2018, modern contraceptive prevalence among all women was 10.5% in Nigeria. IUDs represented 6% of the method mix (7% for married women and 1% for unmarried women). Among married women, the share of IUD is the highest in the South East and South West regions of the country. Almost 80% of IUDs are sourced from the public sector and 20% from the private sector [14]. Recent efforts among both government and non-governmental organizations have been successful in increasing access to family planning including LARCs in Nigeria [15].

The hormonal IUD is not currently available at scale and thus not reflected in national surveys. Since 2007, the International Contraceptive Access (ICA) Foundation, a public-private partnership between Bayer AG and the Population Council, has donated limited quantities of free hormonal IUD devices for distribution by several partners in Nigeria [16]. In 2017, Society for Family Health (SFH) Nigeria began offering donated hormonal IUD units through 40 social franchise clinics in its Healthy Family Network across 18 states spanning all regions of the country. All clinics are located in urban and peri-urban settings and had high pre-existing IUD uptake. At the time of this study, SFH recommended providers charge 3,000 Naira (USD 8.33) for the hormonal IUD, compared to 1,500 Naira (USD 4.17) for implants, 1,000 Naira (USD 2.78) for the copper IUD and 500 Naira (USD 1.39) for injectables.

Design and data collection

At baseline of this prospective study, we surveyed women opting to receive a hormonal IUD, copper IUD, implant or three-month injectable through one of SFH’s 40 social franchise clinics. We conducted a phone survey with a convenience sample of clients within 100 days of method uptake, and follow-up in-depth interviews (IDIs) with a purposive subset of survey participants. Eligible women were clients aged 18–49 who had access to a phone. Family planning providers informed eligible clients and provided the research team with the phone information of those willing to be contacted about the study. We independently confirmed eligibility by extracting the method and date of service from clinic records. Sample size was determined for the prospective study to achieve separate 95% confidence intervals with 5% precision for 12-month continuation rates for each method. We also assumed a 3% intraclass correlation and a 45% loss-to-follow-up rate. Using available information on LARC continuation rates (we used identical assumptions for the copper IUD and the hormonal IUD) [17], we aimed to complete 854 surveys with LARC users at baseline across sites (276 hormonal IUD, 276 copper IUD, 302 implants). We aimed for 50 surveys with injectable users; these were surveyed at baseline only to provide a descriptive comparison of their characteristics to those of LARC users given the popularity of injectables in Nigeria.

We conducted IDIs with a subset of survey participants using a LARC and residing in Oyo (South) or Kaduna (North) state. We purposively selected women to represent a range of contraceptive history and fertility intentions. Given our focus on the hormonal IUD, we aimed for 12–16 IDIs with hormonal IUD acceptors and 12–16 IDIs with other LARC users based on evidence showing these numbers are sufficient to achieve 80% thematic saturation [18].

The baseline survey covered socio-demographic characteristics, contraceptive history, sources of information about the hormonal IUD, reasons for method choice, potential interest in future hormonal IUD use (for women using other methods), and experiences accessing and receiving services. IDI topics included life goals for the next five years, reproductive and contraceptive history, experiences with previous method, reasons for current method selection, experiences obtaining current method, and perceptions of the hormonal IUD. Questions were informed by the existing literature, and revised through peer review, extensive discussions with local study staff, and field pre-test exercises. Surveys and IDIs were conducted in Pidgin English, Yoruba, or Hausa between June and November 2018. Three research assistants administered the survey questionnaire on the phone by using tablets. Four other research assistants conducted IDIs in-person at a pre-arranged location, including participants’ homes or other venues like health facilities. IDIs were audio-recorded and recordings transcribed into English. We obtained verbal consent for the phone survey and written consent for IDIs. Women received 1,000 Naira (USD 2.78) as mobile money for participating in the phone survey and we reimbursed 3,000 Naira (USD 8.33) for transport for IDIs not conducted at home. The National Health Research Ethics Committee in Nigeria and FHI 360’s Protection of Human Subjects Committee in the United States approved the study.

Analysis methods

We compared the characteristics of study participants, reasons for method choice, and experiences obtaining their method descriptively by method received. We then conducted two exploratory multivariable logistic regression analyses to examine the factors associated with uptake of the hormonal IUD relative to the copper IUD and to implants, respectively. We included 12 variables related to socio-demographic characteristics, prior contraceptive use, and partner awareness of baseline method use in all models. We confirmed the absence of multicollinearity using VIF values. Associations were assessed using adjusted odds ratios with their 95% confidence intervals and significance was assessed at the 5% level based on the logistic models. All analyses were done using Stata version 15.

We uploaded IDI transcripts into NVivo 12 for coding and thematic analysis. The codebook combined a priori codes driven by the study’s objectives and data-driven codes that emerged from the reading of transcripts. Coding was divided between four analysts; intercoder agreement was established at the beginning of the process and verified with approximately 10% of transcripts for ongoing consistency. We developed analytic memos to examine the dimensions of each theme and used Excel matrices to summarize the prevalence of key themes.

Results

Survey results

The final sample included 888 women from 39 facilities. From the list of women whom providers referred, 38 women could not be reached and 12 declined participating. We excluded 25 women because they did not meet inclusion criteria upon verification of clinic records.

Characteristics

The mean age by method ranged from 32 to 34 years old and the mean parity from 3.1 to 3.5 (Table 1). Education level, proportion married, and wealth status of social franchise clients were high. Compared to women who chose the injectable or the implant, hormonal IUD and copper IUD acceptors were slightly older, more were in the upper urban wealth quintile, and more wanted to limit childbearing.

Table 1. Participant characteristics.

Hormonal IUD Copper IUD Implant Injectable
n = 266 n = 274 n = 295 n = 53
Age
    18–24 21 (7.9%) 12 (4.4%) 40 (13.6%) 3 (5.7%)
    25–34 127 (47.7%) 130 (47.4%) 148 (50.2%) 28 (52.8%)
    35–49 118 (44.4%) 132 (48.2%) 107 (36.3%) 22 (41.5%)
Mean age (SD) 33.3 (6.1) 33.7 (5.7) 31.7 (6.3) 32.3 (6.1)
Married 258 (97.0%) 262 (96.0%) 273 (92.5%) 47 (88.7%)
Highest education completed
    None or some primary 5 (1.9%) 10 (3.7%) 11 (3.7%) 1 (1.9%)
    Primary 31 (11.7%) 29 (10.5%) 36 (12.2%) 10 (18.8%)
    Secondary 113 (42.5%) 127 (46.4%) 136 (46.1%) 25 (47.2%)
    More than secondary 117 (44.0%) 108 (39.4%) 112 (38.0%) 17 (32.1%)
Parity
    0 5 (1.9%) 2 (0.7%) 10 (3.4%) 3 (5.7%)
    1–2 74 (27.8%) 81 (29.6%) 104 (35.5%) 15 (28.3%)
    3–4 137 (51.5%) 121 (44.2%) 135 (46.1%) 27 (50.9%)
    5+ 50 (18.8%) 70 (25.5%) 44 (15.0%) 8 (15.1%)
Mean number of children (SD) 3.3 (1.5) 3.5 (1.7) 3.1 (1.7) 3.1 (1.7)
Fertility intentions
    Child within 2 years/timing undecided 32 (12.0%) 51 (18.6%) 45 (15.3%) 16 (30.2%)
    Child in 2+ years 85 (32.0%) 64 (23.4%) 107 (36.3%) 11 (20.8%)
    Child, timing undecided 10 (3.8%) 8 (2.9%) 18 (6.1%) 0 (0.0%)
    No more children 93 (35.0%) 114 (41.6%) 90 (30.5%) 17 (32.1%)
    Undecided about more children 46 (17.3%) 37 (13.5%) 35 (11.9%) 9 (17.0%)
Urban Wealth quintilea
    Lowest 4 (1.5%) 5 (1.8%) 7 (2.4%) 2 (3.8%)
    Second 23 (8.6%) 16 (5.9%) 22 (7.5%) 6 (11.3%)
    Middle 29 (10.9%) 31 (11.4%) 38 (13.0%) 8 (15.1%)
    Fourth 50 (18.8%) 54 (19.9%) 67 (22.9%) 11 (20.8%)
    Highest 160 (60.2%) 166 (61.0%) 159 (54.3%) 26 (49.1%)
Full-time or self-employed 197 (74.1%) 200 (73.0%) 191 (64.7%) 37 (69.8%)

a Relative wealth was measured using the equity tool for Nigeria [19]. The urban version of the equity tool compares participants to the urban population in Nigeria.

More injectable users (91%) than LARC users (70–77%) had used a modern method previously (Table 2). Prior use of intrauterine methods was highest among hormonal IUD (20%) and copper IUD (16%) acceptors. Between 55–58% of LARC users and 74% of injectable users reported a short-acting method as their last contraceptive.

Table 2. Contraceptive use history and decision making.

Hormonal IUD Copper IUD Implant Injectable
n = 266 n = 274 n = 295 n = 53
Contraceptive use history
    Ever use of modern contraceptiona 206 (77.4%) 208 (75.9%) 205 (69.5%) 48 (90.6%)
    Ever use of intrauterine method 53 (19.9%) 44 (16.1%) 27 (9.2%) 6 (11.3%)
Last method used
    Hormonal IUD 5 (1.9%) 5 (1.8%) 0 (0.0%) 0 (0.0%)
    Copper IUD 33 (12.4%) 27 (9.9%) 12 (4.1%) 2 (3.8%)
    IUD- unspecified 0 (0.0%) 0 (0.0%) 3 (1.0%) 0 (0.0%)
    Implant 16 (6.0%) 16 (5.9%) 21 (7.1%) 7 (13.2%)
    Injectables 49 (18.4%) 52 (19.0%) 54 (18.4%) 17 (32.1%)
    Pills 18 (6.8%) 29 (10.6%) 28 (9.5%) 4 (7.5%)
    Male condoms 73 (27.4%) 62 (22.7%) 67 (22.8%) 15 (28.3%)
    Emergency contraception 10 (3.8%) 13 (4.8%) 16 (5.4%) 3 (5.7%)
    Other methodb 2 (0.8%) 3 (1.1%) 3 (1.0%) 0 (0.0%)
    No modern method 60 (22.6%) 66 (24.2%) 90 (30.6%) 5 (9.4%)
Used modern method in three months prior to receiving method 104 (39.1%) 77 (28.1%) 88 (29.8%) 27 (50.9%)
Had heard about hormonal IUD at time of survey 266 (100%) 77 (28.1%) 75 (25.4%) 19 (35.8%)
Sources of information about the hormonal IUD c
    Provider during visit for method 207 (77.8%) 75 (97.4%) 69 (92.0%) 17 (89.5%)
    Provider, other visit or referral 39 (14.7%) 3 (1.1%) 4 (1.4%) 1 (1.9%)
    Friends/family 93 (35.0%) 3 (3.9%) 6 (8.0%) 6 (31.6%)
    Community volunteer/IPC agent 44 (16.5%) 2 (2.6%) 2 (2.7%) 2 (10.5%)
Interested in using the hormonal IUD at any time in the future c N/A 57 (74.0%) 50 (66.7%) 13 (68.4%)
Knew prior to visit that they wanted to use method 132 (49.6%) 163 (59.5%) 176 (59.7%) 39 (73.6%)
Made decision without being influenced by others 107 (81.1%) 136 (83.4%) 146 (83.0%) 36 (92.3%)
Partner aware of baseline method use 236 (89.4%) 248 (91.2%) 267 (91.1%) 43 (81.1%)

IPC = Interpersonal communication.

a For the purposes of this analysis, modern methods include the hormonal IUD, the Copper IUD, implants, injectables, pills, emergency contraception and male and female condoms.

b Other methods include female condoms and standard days method.

c Among women who had heard about the hormonal IUD. Multiple responses possible.

Method choice

Between 25–36% of women who chose other methods had heard about the hormonal IUD prior to the survey. Providers were the most common source of information about the hormonal IUD. Compared to other method users, fewer hormonal IUD acceptors said they already knew they wanted to use the method they received when they went to the clinic (50% vs. 60–74%). More injectable users (92%) than LARC users (81–83%) said they chose their method without being influenced by others. Over 89% of LARC users and 81% of injectable users reported that their partner knew they were using their method.

In the multivariable models (Table 3), we did not find any significant association between any of the covariates and hormonal IUD use relative to copper IUD use. Married women and women who had previously used a LARC had higher odds of using the hormonal IUD relative to implants, while women whose partner was aware of method use had higher odds of implant use.

Table 3. Adjusted odds ratio estimates and 95% confidence interval from logistic regression analyses associated with choosing the hormonal IUD over other methods.

Characteristic (reference group) Hormonal IUD vs. copper IUD Hormonal IUD vs. implant
(n = 538) (n = 557)
Variables OR (95% CI) OR (95% CI)
Age 0.997 (0.961–1.034) 1.025 (0.988–1.064)
Currently married 1.589 (0.574–4.401) 3.067 (1.097–8.577)
Completed secondary school 1.086 (0.631–1.869) 1.343 (0.781–2.310)
Wealth categories (1st-3rd)
    Fourth 0.803 (0.454–1.422) 0.751 (0.430–1.310)
    Highest 0.835 (0.517–1.348) 0.937 (0.584–1.505)
Full-time or self-employed 1.094 (0.730–1.640) 1.242 (0.834–1.850)
Parity 0.911 (0.775–1.071) 0.970 (0.823–1.142)
Fertility intentions (no/no more children)
    Undecided about having more children 1.401 (0.808–2.429) 1.501 (0.853–2.640)
    More children, in >2 years 1.449 (0.848–2.476) 1.065 (0.637–1.778)
    More children, within 2 years or undecided timing 0.748 (0.414–1.349) 0.921 (0.508–1.671)
Prior contraceptive use (never used a modern method)
    Used any IUD or IUD 1.479 (0.811–2.697) 2.927 (1.527–5.612)
    Used other modern method 1.047 (0.668–1.643) 1.396 (0.907–2.149)
Prior experience of increased bleeding 0.834 (0.505–1.377) 1.331 (0.767–2.310)
Prior experience of reduced bleeding or amenorrhea 1.253 (0.697–2.255) 0.781 (0.451–1.353)
Prior experience of bleeding disturbances 1.228 (0.767–1.966) 0.820 (0.512–1.315)
Partner aware of baseline method use 0.707 (0.388–1.289) 0.512 (0.262–1.001)

Age and parity are interval variables. Other variables are yes/no binary variables, with no as the reference level or categorical variables with the reference level included in parentheses. For urban wealth quintiles, the reference level combines the three lowest quintiles. Statistically significant values (p≤ 0.05) are bolded.

A perception that the method was “right for my body,” long duration, recommended by provider, recommended by friends/family, few/manageable side effects, and high effectiveness were cited as reasons for method choice by at least 25% of women across LARCs (Fig 1). Among hormonal IUD users, 17% mentioned reduced bleeding (inclusive of lighter, shorter or no period), and 16% mentioned treatment of heavy or painful period.

Fig 1. Reasons for method choice.

Fig 1

When asked what method they would have chosen if the method they received had not been available, between 25% and 33% of women said they would have chosen no method (Fig 2). Among hormonal IUD acceptors, 23% would have chosen implants, 19% a copper IUD, and 14% a short-acting method. Copper IUD users would most commonly have selected an implant (22%), whereas implant users would have primarily selected injectables (16%) or the copper IUD (13%). The most common responses among injectable users were short-acting methods like condoms (13%) or pills (11%).

Fig 2. Method client would have chosen if method received was unavailable.

Fig 2

Among those who were not using a hormonal IUD but had heard about the method (n = 171), 74% of copper IUD users, 67% of implant users and 68% of injectable users said they may be interested in using the hormonal IUD at some point in the future (Table 2). Of the 51 women who said they would not use the hormonal IUD, the main reason, was fear of the insertion procedure.

Experiences obtaining methods

Between 85–91% of women recalled being counseled on other methods, and 68% of injectable users and 83–85% of LARC users reported being informed about contraceptive-induced menstrual changes (CIMCs) and/or other non-bleeding side effects (Table 4). Among women who said they were counseled on side effects, the type of CIMCs women most commonly reported being counseled on was bleeding disturbances (defined as changes in frequency, spotting, or irregular periods). When looking at the menstrual disruptions that can commonly be expected for each method, among women counseled, 60% of copper IUD users said they were told about heavier or prolonged bleeding, while 48% of hormonal IUD acceptors recalled being told about lighter or shorter bleeding, 29% about amenorrhea, 32% about heavier or prolonged bleeding, and 16% about reduced menstrual pain.

Table 4. Experience with counseling and services.
Hormonal IUD Copper IUD Implant Injectable
n = 266 n = 274 n = 295 n = 53
Told by provider about other methods 239 (89.8%) 232 (84.7%) 258 (87.5%) 48 (90.6%)
Told about CIMCs and/or non-bleeding side effects 227 (85.3%) 230 (83.9%) 244 (82.7%) 36 (67.9%)
Non-bleeding side effects mentioned by provider, %a
    Weight gain 87 (38.3%) 76 (33.0%) 106 (43.4%) 13 (36.1%)
    Abdominal pain 51 (22.5%) 43 (18.7%) 29 (11.9%) 3 (8.3%)
    Headaches 50 (22.0%) 55 (23.9%) 87 (35.7%) 4 (11.1%)
    Mood changes 17 (7.5%) 9 (3.9%) 21 (8.6%) 0 (0.0%)
    Nausea/vomiting 16 (7.0%) 23 (10.0%) 41 (16.8%) 3 (8.3%)
    Other 36 (15.9%) 54 (23.5%) 25 (10.2%) 4 (11.1%)
    Any type 131 (57.7%) 138 (60.0%) 151 (61.9%) 17 (47.2%)
CIMCs mentioned by provider, %a
    Bleeding disturbances 190 (83.7%) 180 (78.3%) 197 (80.7%) 23 (63.9%)
    Lighter or shorter bleeding 108 (47.6%) 74 (32.2%) 84 (34.4%) 5 (13.9%)
    Heavier or longer bleeding 72 (31.7%) 137 (59.6%) 121 (49.6%) 13 (36.1%)
    No bleeding 66 (29.1%) 29 (12.6%) 48 (19.7%) 10 (27.8%)
    Less pain during period 37 (16.3%) 4 (1.7%) 0 (0.0%) 0 (0.0%)
    Any type 219 (96.5%) 220 (95.7%) 227 (93.0%) 31 (86.1%)
Correctly reported method duration b 240 (90.2%) 211 (77.0%) 210 (79.5%) 49 (92.5%)
Told by provider at insertion that method can be removed at any time they want 260 (97.7%) 265 (96.7%) 282 (95.6%) N/A
Told at insertion where removal can be obtained, %
    Insertion place only 151 (56.8%) 150 (54.7%) 160 (54.2%) N/A
    At any clinic 89 (33.5%) 103 (37.6%) 111 (37.6%) N/A
    Not told about any place, don’t know 26 (9.8%) 21 (7.7%) 24 (8.1%) N/A
Felt privacy sufficient when received method 249 (93.6%) 258 (94.2%) 274 (92.9%) 52 (98.1%)
Experienced problems when received method 88 (33.1%) 91 (33.2%) 77 (26.1%) 4 (7.5%)
Median price paid for method (N) 3000 1500 1500 500
Obtained method during first clinic visit 210 (78.9%) 226 (82.5%) 247 (83.7%) 46 (86.8%)

CIMCs = Contraceptive-induced menstrual changes.

a Among women counseled on CIMCs and/or non-bleeding side effects. Multiple responses possible.

b Based on the duration participants recalled being told by providers when receiving the method. For implants, correct duration was determined based on implant type as informed by participant reports of the number of rods in their implants. Those who did not know their implant type (n = 31) were excluded.

Overall, 90% of hormonal IUD acceptors, and 77–80% of other LARC users correctly reported the duration of their method. Over 95% of LARC users across methods were told by the provider that they could remove their method at any time; however, over half were not told about any other place their method could be removed besides where it was inserted.

Over 92% of women said there was sufficient privacy during the insertion procedure. Just over a quarter (26%) of women who received an implant and 33% of those who received a copper IUD or a hormonal IUD reported experiencing problems when they received the method, compared with 8% of injectable users. Few problems were reported besides temporary pain or discomfort.

Over 78% of women obtained their method during their first visit to the clinic. Reasons for not getting a method the first time included having come to the clinic to get information only, needing partner approval first, or the provider being unavailable.

IDI results

There were 32 IDIs, conducted with 17 hormonal IUD, 4 copper IUD and 11 implant acceptors. Most IDIs were conducted within 30 days of the survey, and all within 16 weeks. Here we organized results according to the considerations that led women to choosing a method and to contextual barriers, with particular attention to factors supporting or hindering hormonal IUD uptake. Because reduced menstrual bleeding is a distinctive feature of the hormonal IUD, interviews probed to establish women’s perspectives on reduced bleeding and amenorrhea more broadly and findings related to this theme are presented separately.

Women’s considerations related to method choice

Respondents highlighted similar appealing method characteristics across LARCs. Nearly two-thirds said that the effectiveness and extended duration of their method gave them peace of mind that no pregnancy would occur, allowing them not to worry when having sex, to raise their children properly, and to focus on work. Many women noted the greater reliability and convenience of LARCs over injectables and pills due to reduced user involvement and fewer clinic visits. Several hormonal IUD and copper IUD acceptors appreciated that return to fertility would be immediate. A 27-year-old hormonal IUD user said:

If I am not carrying a child or pregnant, I have the freedom to work, but if you have a child and you have a baby, you are not so free to work so that is the benefit…in five years, I will be able to contribute significantly to my family and even if I get pregnant, I will not be under pressure to buy baby things, and my child will not be looking dirty.—A223

Finding a method with minimal or tolerable side effects was important in selecting a method for many women, especially hormonal IUD users. Across methods, several women who had a prior negative experience with contraception were motivated to find a different method that would not cause the same problem, while a few others preferred staying on a method that worked well for them. Six of the 17 hormonal IUD acceptors specifically mentioned reduced bleeding as a motivation for choosing the hormonal IUD. Of these, four had previously experienced heavy bleeding with the copper IUD. Another participant chose the hormonal IUD after experiencing dysmenorrhea with the copper IUD. Several women across methods mentioned that their goal was to minimize effects on menstruation, like this hormonal IUD user who was a first-time contraceptive user: “I look for options that are as close to the normal thing as possible” (A111).

Although some participants acknowledged that experiences with a method may vary across women, many indicated that hearing about others’ experience–typically close friends or relatives—was a deciding factor, as explained by this 30-year-old hormonal IUD user:

I saw others doing it and none of them had any complaint of headache or anything. So, I said, okay, let me do something that will give me peace.–A133

Among hormonal IUD users specifically, several women reporting earlier challenges with side effects or method effectiveness explained they selected the hormonal IUD after the provider recommended it as a better option. A few other hormonal IUD users explained they were convinced to take up the method based on the information received from the provider. Several hormonal IUD users explained they decided to give the method “a try,” as explained by this 33-year-old woman who started the method a few months after giving birth to her third child:

It was the nurse that told me about it. She told me that they have brought a new [method] and that it may be better than the other ones. Then, I said, okay, let me just use it and see.–A122

Several participants, including some implant users but also a few hormonal IUD acceptors, expressed concerns around intrauterine placement, including dislike of exposing themselves and not wanting their sexual partner to feel strings during sex, as well as fear of damage inside the womb, of experiencing pain during sex, or of migration to the stomach. At the same time, some women reported they did not like injections. A few women who chose intrauterine methods said that this mode of delivery was more discreet, caused less pain, or felt it was less invasive than inserting an implant.

Contextual barriers

Most women, especially hormonal IUD acceptors, acknowledged needing partner permission to use family planning. Many women indicated that their partner agreed to a specific method, while some women said their partners had no opinion and a few women’s partners recommended the method themselves. Several participants reported discussing side effects with their partner when seeking permission or evaluating methods together, including this 42-year-old hormonal IUD user who was previously experiencing heavy bleeding with a copper IUD:

[I talked with] my husband…because I have to tell him anything I want to do before I do it…. He said I can change [my copper IUD] because he knows I was having challenges, so immediately I said I want to change it. He said, okay, I should go and change it.–A132

More hormonal IUD users than copper IUD and implant users in the sample did not obtain their method the first time they went to the clinic. Among hormonal IUD users who returned a second time, several indicated they had not brought enough money to the initial visit, and a few explained that they needed to discuss with their partner. Two hormonal IUD users and one implant acceptor reported they had to return due to lack of equipment or staff at the facility. Many hormonal IUD users and one copper IUD acceptor indicated receiving financial support from their partner to pay for their method, including two whose husbands accompanied them to the clinic.

Perspectives on reduced bleeding and amenorrhea

IDIs discussed the acceptability of reduced bleeding and amenorrhea through women’s reports of their experiences and direct probing around perceptions of lighter bleeding and amenorrhea. Twenty-six of the 32 participants expressed concerns related to amenorrhea. While several women said they were not worried about or saw advantages to not menstruating, some of them expressed concerns about amenorrhea in the same interview. Similarly, when asked specifically if they would prefer to experience reduced bleeding or no bleeding, twice as many women favored reduced bleeding while others contradicted themselves. Underlying perceptions of amenorrhea were considerations related to general health and pregnancy. The most common concern was related to “dirt” accumulating in the body in the absence of a period to flush it out. Several women perceived that not having a period was unnatural, contrary to the will of God, or would interfere with “feeling like a woman.” Many said that being amenorrhoeic would cause them to be worried about pregnancy status. Additionally, a few women were concerned that amenorrhea could affect their fertility, but a similar number said they knew fertility would return after discontinuing method use. Illustrating the contradictory nature of statements made by some women, one implant user said:

Some women did the family planning and did not see their period and they are living okay. So, I will be okay with it if I don’t see my period…to me, it’s not okay for [a] woman not to see her period. A woman is supposed to be seeing her period every month. Because I might feel the thing is affecting your stomach somewhere.–R113

The perceived or experienced benefits that participants mentioned in relation to amenorrhea were similar to those they associated with reduced bleeding. These included lifestyle improvements ranging from better menstrual hygiene management (e.g., using fewer or no pads and not having to wash blood) to greater freedom. One hormonal IUD user who previously used baby diapers to manage heavy bleeding with the copper IUD said:

The money for that pampers now, I don’t buy pampers again because I will not use it…I can save the money, so it’s important because I can save something for my business [frying food but saving to open a shop]… that time that I was using [pampers] during my heavy flow, I will not go out for my business but now I am, I can go at any time any day, every day I used to go and I save some money.–A131

Notably, some factors emerged from the interviews that appeared to influence perceptions of amenorrhea. A few hormonal IUD acceptors who did not want any more children explained that their concerns about amenorrhea were reduced now that they were done with childbearing. A few women also explained that they were not bothered by amenorrhea experienced while using contraception postpartum because they were still breastfeeding or had given birth less than six months earlier and felt it was natural.

Discussion

This study among social franchise clients across 18 states in Nigeria contributes information on the user population for the hormonal IUD relative to other LARCs and injectables, and on the factors affecting uptake of this method. Together with condoms, implants and injectables lead the method mix in Nigeria, especially among married women, while copper IUD use is more limited and population surveys do not report on the hormonal IUD [14]. Altogether, characteristics of women in our sample were generally consistent with those of contraceptive users in Nigeria, where contraceptive use is more common among women who are married, have 3–4 children, are more educated, and have greater household wealth [14]. Among adopters of the four contraceptive methods, we generally found few differences in the socio-demographic profile and contraceptive history of participants. Multivariable results did not reveal significant differences between copper IUD and hormonal IUD users. Hormonal IUD users were more likely to be married, to have prior experience with LARCs and to use their method unbeknownst to their partner compared to implant users. About a quarter of clients who chose each LARC were first-time users of modern contraception indicating the strong potential of all LARCs, including the hormonal IUD, to reach new users in the study setting.

Findings reaffirm the importance of offering a robust contraceptive mix that allows women to choose a method based on their preferences. Between a quarter and a third of women would have walked away without a method if their preferred option had not been available. Regarding the hormonal IUD specifically, our findings are similar to other results showing that the hormonal IUD does not just substitute for other LARCs [9]. Rather, many women would have chosen a short-acting method or not taken any method had the hormonal IUD not been available.

Quantitative and qualitative results indicate that the features driving women to choose the hormonal IUD reside in a combination of characteristics shared with other LARCs as well as distinct elements. Appealing characteristics that were shared with other LARCs include duration of protection against pregnancy and very high effectiveness. LARCs also afforded additional convenience linked to reduced clinic visits and user involvement. Although injectables are generally very effective, that was not a common motivator for their use in this study. Conversely, discreetness and affordability were disproportionately given as reasons for choosing injectables compared to LARCs. Notably, between 10 and 20% of LARC users reported wanting another child within the next two years, signaling that the benefits of LARCs attract women who may not intend to use them until their labeled duration of use. Supporting this notion are qualitative findings describing women’s desire to delay pregnancy in order to have more freedom to focus on the children they have and/or work.

Unique features of the hormonal IUD that contributed to uptake among users include potential for reduced side effects, reduced or paused bleeding, and treatment for menorrhagia. While both quantitative and qualitative findings showed that these elements influenced method choice, they generally did not figure as prominently in the results as the characteristics shared with other LARCs. Several factors may explain this. First, method selection is heavily informed by a combination of information received from other women and personal experience. To date, however, the number of users and, consequently, the availability of experiential input on the hormonal IUD are limited. In the future, enabling women to speak with champion users could prove a valuable strategy. Second, while women’s perceptions of reduced bleeding are favorable, concerns over amenorrhea persist, including beliefs around blood accumulation in the womb and fear that absence of bleeding is a sign of pregnancy. This is consistent with what has been reported elsewhere [20]. Third, our findings uncovered possible gaps and inconsistencies in counseling on CIMCs and non-bleeding side effects. A sizable minority of women did not recall being counseled on side effects, especially among injectable users, or about common side effects of the method they received. Examples include the possibility of lighter or shorter bleeding with the hormonal IUD or of heavier or longer bleeding with the copper IUD. Additionally, some of the side effects clients reported being counseled on are not typical of their method, such as weight gain for the copper IUD. Counseling tools, including client-facing adaptations, could be valuable to increase knowledge of potential bleeding disruptions among women. One example is the NORMAL job aid, which includes a description of the types of CIMCs that may be expected over time with each method [21]. Importantly, our results also point to the need to address both health and lifestyle implications in messaging. One encouraging finding is the evidence of communication on when and where removal can be procured for LARCs, including the possibility of removing a method prior to its expiration date. Access to removal services is an essential component of rights-based family planning that is receiving increasing attention, especially given unprecedented growth in implant use in sub-Saharan Africa [2224].

Previous evidence suggests that low uptake of the copper IUD is often due to both provider-side barriers (e.g., lack of comfort or willingness to insert the method) and client-side concerns (e.g., persistent myths and misperceptions) [7]. Fears among potential users related to uterine placement have been shown to constrain copper IUD uptake, which may be a barrier to hormonal IUD uptake as well [25]. While fear of insertion was the main deterrent for women who said they would not use the hormonal IUD at any point in the future, over two thirds of the women who received other methods expressed interest in using the hormonal IUD in the future. Moreover, some women in our qualitative sample were hormonal IUD users who had overcome initial fears surrounding insertion and other aspects of intrauterine placement. Although possible courtesy bias should be kept in mind, taken together, these results indicate that intrauterine placement is not an insurmountable barrier to uptake of the hormonal IUD.

Partner support can affect contraceptive use [26, 27]. Although the methods in this study have potential for discreet use, partner awareness of use was high across the four methods, especially for injectables. In the multivariable analyses, hormonal IUD users were more likely than implant users to use their method discreetly. Qualitative results indicate that while women typically needed partner permission to use contraception, men were less influential in method choice. Financial support by partners was also important, as has been found in other research [28].

Findings highlight lack of awareness of the method as a potential barrier to hormonal IUD uptake. This was similarly identified as a constraint by providers in a recent assessment across five service delivery settings in Nigeria [29]. As demand generation efforts have remained limited to date, knowledge of and demand for the hormonal IUD are largely provider-driven. In this study, the majority of women who chose other methods had not heard about the hormonal IUD. While recall issues have to be considered, given that the method was available at all service delivery points from which women were recruited, this may suggest either gaps in counseling on the full range of available methods or conflation between the copper IUD and the hormonal IUD.

Limitations

The study population is limited to social franchise clients with phones; education and wealth may be higher than in other settings. Most women in this study were over the age of 25. Although some hormonal IUD introduction efforts have been successful in reaching younger women, more research is needed with younger populations. Social franchise clinics prioritized for hormonal IUD introduction by SFH had high copper IUD uptake and were typically located in urban and peri-urban settings [13]. While this survey of clients across 18 states provides broad geographic and cultural representation, the setting may be particularly conducive to introduction of the hormonal IUD and findings may not easily transfer to other contexts. Recruitment through providers and the requirement that women have and share phone contact details carry a risk of selection bias. The analysis does not differentiate between types of implants. Survey questions do not allow reporting on the method information index as a measure of quality. Our study design does not enable us to determine if some women failed to get a method due to inability to pay for the hormonal IUD.

Conclusions

Broader introduction of the hormonal IUD provides an opportunity to expand LARC choices for women in Nigeria, and the government in Nigeria currently plans to scale up the method including in the public sector. Characteristics shared with other LARCs were attractive; unique distinctive features of the hormonal IUD are appealing but potentially less well-known. Limited awareness of the method and gaps in counseling are barriers that need to be addressed to realize the full potential of the method.

Acknowledgments

The study team thanks Ms. Aderonke Popoola and Mr. Ekerette Emmanuel Udoh for support to study implementation. We acknowledge the contributions of Ms. Claire Brennan to the analysis of qualitative data. We are also thankful to Ms. Samantha Archie for her help in verifying study results. Special acknowledgment goes to Dr. Jennifer Anyanti, Dr. Oluwole Fajemisin, and Dr. Hadiza Khamofu for supporting this study. We thank Dr. Laneta Dorflinger, Dr. Theresa Hoke and Dr. Mario Chen for their careful review of this manuscript.

Data Availability

The de-identified survey dataset, the survey questionnaire, and the in-depth interview guide are publicly available online through the Harvard Dataverse (https://dataverse.harvard.edu/dataverse/fhi360_leap). Full qualitative transcripts are not available for ethical reasons because of the risk of deductive disclosure. However, relevant excerpts of transcripts are available from the authors on reasonable request.

Funding Statement

KR Investment number: INV-008333 Project title: Learning about Expanded Access and Potential of the LNG-IUS (LEAP) Initiative Funder: Bill & Melinda Gates Foundation https://www.gatesfoundation.org/ The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

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Decision Letter 0

Federico Ferrari

22 Jul 2021

PONE-D-21-10209

Factors affecting uptake of the levonorgestrel intrauterine system: A mixed-method study of social franchise clients in Nigeria

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Reviewer #1: Excellent article and important contribution to the literature. Recommend acceptance with just a few comments.

1. Study setting: It would be helpful to provide more information about the location of the 18 states where SFH has been distributing hormonal IUS - which regions of the country?

2. Were injectable users all using DMPA-IM? Probably worth noting availability of DMPA-SC/SI at the time of the study as a background contextual factor.

3. I'm surprised that assumed continuation rates for the copper IUS and the LNG IUS are the same, is that really widely borne out in research?

4. The fact that a lower proportion of injectable users were told about bleeding changes (and really, side effects generally) seems worth mentioning somewhere in terms of programmatic implications, especially given all the literature on the importance of counseling on this issue. Or do you think it's because many were continuing/previous injectable users who were already familiar?

5. Discussion: "Appealing characteristics that were shared with other LARCs but not injectables include duration of protection against pregnancy and very high effectiveness." In order to avoid misunderstandings/misperceptions among readers, I wonder if it's worth adding something like "(although injectables are generally very effective, that did not seem to be a motivator for their use in this study") or something along those lines. I also wonder if it's worth noting that affordability and discretion were downsides for LARCs in the study in terms of the importance of reinforcing the importance of method mix.

6. Curious why demand generation efforts have been so limited, can you briefly explain?

7. Probably worth mentioning the results on removal in the discussion and what these results add to that important area of work on LARCs.

8. The age profile of the population in this study is an important limitation, and could reinforce misperceptions that LARCs are not good choices for AGYW. Please add to limitations and flag as an important area for research and evidence generation in settings like Nigeria (or link to research/evidence that exists).

Reviewer #2: Review: Factors affecting update of hormonal IUS in Nigeria PLOS ONE

This study captures information on the socio-demographic profile and experiences of women receiving LARCs or Injectables at private facilities in Nigeria, combining quantitative and qualitative methods. The study aims to provide a quantitative comparison of Hormonal IUS users as compared to other LARC users, and then probes for particular details on experiences before and after the method was accepted.

The study is sound, if limited in its generalizability. Some requests for revision are provided.

1) Line 61-64: The summary of findings form 4 other studies, grouped together with wide ranges in the values, is confusing. Present it in more detail.

2) Line 104-106: Upon reading the results, I expected to see statistical comparisons between LARC and injectable users. Going back to methods, I see why this may not be possible. But in this case, it seems that there is not enough emphasis on how or if LARC users in this study are similar to, or different from, other contraceptive users in Nigeria. How do the injectable users at the franchised facilities compare to other urban contraceptive users, as per DHS data? How are the clients of these facilities similar to or different from other contraceptive users in Nigeria? This context is important – can be provided in intro, or discussion.

3) Line 148: Specify that means are presented by method, else we would expect a single mean.

4) Table 1: Mean(SD) for age is not a percentage. The EquityTool is written thus.

5) Table 3: Consider using age categories. Wealth category descriptions are misleading – rename ‘middle’ to 4th, lowest to (1st-3rd).

6) Table 4: Is it possible from the data to calculate the Method Information Index? If so, this should be reported. If not, add as limitation. Further, please comment further in discussion on how some of the side effects and bleeding changes reported by clients in relation to the method they received are not considered as known side effects of that method (ie – weight gain w copper IUD).

7) Line 279: Do you have any information in the IDIs regarding cost of the method as a criteria for selection? Given that the hormonal IUS used by SFH were donated commodities, can you further describe or reflect on the implications of their pricing strategy? Why would they be priced at 3x that of the copper IUD, when, presumably, the profit for the donated commodity would be greater even if priced equally? How does price influence use? What does that mean for Nigeria’s public sector strategy?

8) Line 334-335: This seems to be a good place to provide context, comparing study participant profile with that of users from DHS data.

9) Line 345-346: Check grammar.

10) Line 366-369: Consider explicitly commenting on provider knowledge related to LARCs, and reference other literature in this area.

11) Line 382-386: Greater discreet use for the more expensive method, and financial support from partners, seem in contradiction. Elaborate.

**********

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Reviewer #1: No

Reviewer #2: Yes: Nirali M Chakraborty

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PLoS One. 2021 Sep 29;16(9):e0257769. doi: 10.1371/journal.pone.0257769.r002

Author response to Decision Letter 0


3 Sep 2021

Responses to reviewer comments

Submission: “Factors affecting uptake of the levonorgestrel intrauterine system: A mixed-method study of social franchise clients in Nigeria” - PONE-D-21-10209

Other

• Editor - Data availability statement: The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository.

Thank you. We have added a data availability statement.

• Editor - Please ensure that you include a title page within your main document. We do appreciate that you have a title page document uploaded as a separate file, however, as per our author guidelines (http://journals.plos.org/plosone/s/submission-guidelines#loc-title-page) we do require this to be part of the manuscript file itself and not uploaded separately. Could you therefore please include the title page into the beginning of your manuscript file itself, listing all authors and affiliations.

The title page was included in the manuscript file.

• Please note: The World Health Organization released an announcement about the nomenclature for the levonorgestrel-releasing intrauterine device after the paper was first submitted. We changed the name to hormonal IUD throughout the paper to align with this guidance.

Introduction

• R2 - Line 61-64: The summary of findings form 4 other studies, grouped together with wide ranges in the values, is confusing. Present it in more detail.

We added more details about the findings from each study.

Methods

• R1 - Study setting: It would be helpful to provide more information about the location of the 18 states where SFH has been distributing hormonal IUS - which regions of the country?

The 18 states in which the SFH facilities span all regions in the country. They include Kaduna, Kano, Katsina (North West), Gombe, Taraba (North East), Benue, Niger, FCT (North Central), Lagos, Ogun, Oyo, (South West), Abia, Enugu (South East) and Cross River, Akwa Ibom, Edo, Delta and Rivers (South South). We added that the states span all regions of the country.

• R1 - Were injectable users all using DMPA-IM? Probably worth noting availability of DMPA-SC/SI at the time of the study as a background contextual factor.

Thank you for this question. Only DMPA-IM was available from the study sites when the study was conducted.

• R1 - I'm surprised that assumed continuation rates for the copper IUS and the LNG IUS are the same, is that really widely borne out in research?

There was very little information on continuation rates for the hormonal IUD compared to other methods in sub-Saharan Africa when we designed the study. A cohort study of postpartum women in Kenya found no statistically significant differences between 12-month continuation rates among hormonal IUD and implant users (89% and 92%, respectively); results for the Cu-IUD were not reported due to low uptake. In a prospective cohort study in the United States, the hormonal IUD had a one-year continuation rate of 87%, compared with 84% for the Cu-IUD and 82% for the three-year subdermal implant. The longitudinal results from the present study and a companion study conducted in Zambia were just published in The Lancet Global Health. Twelve-month continuation rates were 87% for the hormonal IUS and copper IUD, and 85% for implants in Nigeria. In Zambia, they were 95% for the hormonal IUS, 89% for the copper IUD, and 83% for implants. In Zambia, time-to-event curves for the implant and the hormonal IUS were statistically different. We did not find any statistically significant differences between the hormonal IUD and the Cu-IUD.

• Editor - Please state whether you validated the questionnaire prior to testing on study participants. Please provide details regarding the validation group within the methods section.

Survey questionnaires were informed by a review of the existing literature and jointly developed by study staff in the US and Nigeria, after which they underwent independent peer review by FHI 360 staff. Prior to each data collection round, the questionnaires were discussed extensively and tested through role play during data collector training. We made adjustments to the wording of the questions and the pre-coded responses in all local languages based on the feedback of study supervisors and data collectors working directly with similar populations. We then conducted a field pre-test exercise with a population exhibiting similar characteristics to those of study participant groups to inform final adjustments. We similarly pre-tested qualitative topic guides and used the information from pre-test qualitative interviews to ensure that all important themes coming in the responses were captured in the survey pre-coded responses. We added a sentence describing this process to the methods section.

• Editor - Please include additional information regarding the survey or questionnaire used in the study and ensure that you have provided sufficient details that others could replicate the analyses. For instance, if you developed a questionnaire as part of this study and it is not under a copyright more restrictive than CC-BY, please include a copy, in both the original language and English, as Supporting Information.

• Editor - Please include a copy of the interview guide used in the study, in both the original language and English, as Supporting Information, or include a citation if it has been published previously.

Thank you. The survey and interview guide are publicly available online through the Harvard Dataverse. We indicated this as part of the data availability statement. The questionnaires were developed in English; translated versions are not available as Word document as they were entered directly in the ODK programs.

Results

• R2 - Line 148: Specify that means are presented by method, else we would expect a single mean.

Thank you. We made this edit.

• R2 - Table 1: Mean(SD) for age is not a percentage. The EquityTool is written thus.

Thank you. We edited Table 1.

• R2 - Table 3: Consider using age categories. Wealth category descriptions are misleading – rename ‘middle’ to 4th, lowest to (1st-3rd).

Thank you. We considered using age categories, but ultimately decided against it because we had few people in the lowest and smallest age groups. We have renamed the Wealth categories as suggested.

• R2 - Table 4: Is it possible from the data to calculate the Method Information Index? If so, this should be reported. If not, add as limitation.

The survey collected information on whether clients were informed about other methods and whether they were told about side effects. However, we did not collect information on whether clients were told what do if they experienced side effects. Therefore, we are not able to report on the MII. This was added to limitations.

• R2 - Line 279: Do you have any information in the IDIs regarding cost of the method as a criteria for selection? Given that the hormonal IUS used by SFH were donated commodities, can you further describe or reflect on the implications of their pricing strategy? Why would they be priced at 3x that of the copper IUD, when, presumably, the profit for the donated commodity would be greater even if priced equally? How does price influence use? What does that mean for Nigeria’s public sector strategy?

Thank you for this insightful question. As indicated in the manuscript, several participants described the need to go collect the necessary funds with which they would return to the health facility another day, but cost was not a major theme described by IDI participants relating to whether or not to select the method. More broadly, the reason for the higher price for the hormonal IUD in the pilot setting was that SFH anticipated that the method would ultimately be scaled up as a “premium product” given commodity costs for commercial products at the time. Therefore, they wanted to start building the market with this in mind. However, since that time, the hormonal IUD has been added to the UNFPA and USAID catalogs at a more affordable public sector price; as such, the ultimate pricing structure in social franchise settings is still being determined in consultation with suppliers and donors. We feel that this level of detail is not appropriate for this manuscript but we could add a footnote with this background information if the editors request it.

Discussion

• R1 - The fact that a lower proportion of injectable users were told about bleeding changes (and really, side effects generally) seems worth mentioning somewhere in terms of programmatic implications, especially given all the literature on the importance of counseling on this issue. Or do you think it's because many were continuing/previous injectable users who were already familiar?

• R2 - Further, please comment further in discussion on how some of the side effects and bleeding changes reported by clients in relation to the method they received are not considered as known side effects of that method (ie – weight gain w copper IUD).

We expanded this section of the discussion.

• R2 - Line 366-369: Consider explicitly commenting on provider knowledge related to LARCs, and reference other literature in this area.

Thank you. We added a comment about provider-side barriers to copper IUD provision which may be applicable to hormonal IUD provision as well.

• R1 - Discussion: "Appealing characteristics that were shared with other LARCs but not injectables include duration of protection against pregnancy and very high effectiveness." In order to avoid misunderstandings/misperceptions among readers, I wonder if it's worth adding something like "(although injectables are generally very effective, that did not seem to be a motivator for their use in this study") or something along those lines. I also wonder if it's worth noting that affordability and discretion were downsides for LARCs in the study in terms of the importance of reinforcing the importance of method mix.

We added these points.

• R1 - Curious why demand generation efforts have been so limited, can you briefly explain?

For demand creation, SFH used a provider-initiated awareness generation model. This involved the provider carrying out talks about contraception with women in the facilities who came for postnatal or child wellness visits. In these contexts, the provider would include the hormonal IUD in the context of a full method mix; there were not dedicated demand creation activities focused solely on this method. The approach is described further in a 2020 publication that is cited in this paper; see Brunie A, Rademacher KH, Nwala AA, Danna K, Saleh M, Afolabi K. Provision of the levonorgestrel intrauterine system in Nigeria: Provider perspectives and service delivery costs. Gates Open Res. 2020;4.

• R1 - Probably worth mentioning the results on removal in the discussion and what these results add to that important area of work on LARCs.

We added this to the discussion.

• R1 - The age profile of the population in this study is an important limitation, and could reinforce misperceptions that LARCs are not good choices for AGYW. Please add to limitations and flag as an important area for research and evidence generation in settings like Nigeria (or link to research/evidence that exists).

• R2 - Line 104-106: Upon reading the results, I expected to see statistical comparisons between LARC and injectable users. Going back to methods, I see why this may not be possible. But in this case, it seems that there is not enough emphasis on how or if LARC users in this study are similar to, or different from, other contraceptive users in Nigeria. How do the injectable users at the franchised facilities compare to other urban contraceptive users, as per DHS data? How are the clients of these facilities similar to or different from other contraceptive users in Nigeria? This context is important – can be provided in intro, or discussion.

• R2 - Line 334-335: This seems to be a good place to provide context, comparing study participant profile with that of users from DHS data.

We added some information on the profile of contraceptive users in Nigeria in the discussion section. As noted under limitations, we also agree that the generalizability of our findings is likely to be limited because the study is focused on social franchise clients with phones. We expect that education and wealth among study participants may be higher than in other settings. We added a brief discussion of the age profile to the limitations.

• R2 - Line 345-346: Check grammar.

Thank you; this has been addressed.

• R2 - Line 382-386: Greater discreet use for the more expensive method, and financial support from partners, seem in contradiction. Elaborate.

While discreet use was significant in the model comparing the hormonal IUD to implants, as shown in Table 2, male partners were by and large aware of method use. Thus we do not believe that this finding contradicts the one on financial support from partners.

Attachment

Submitted filename: Responses_reviewers.docx

Decision Letter 1

Federico Ferrari

10 Sep 2021

Factors affecting uptake of the levonorgestrel-releasing intrauterine device: A mixed-method study of social franchise clients in Nigeria

PONE-D-21-10209R1

Dear Dr. Rademacher,

We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements.

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Kind regards,

Federico Ferrari

Academic Editor

PLOS ONE

Additional Editor Comments (optional):

Reviewers' comments:

Acceptance letter

Federico Ferrari

20 Sep 2021

PONE-D-21-10209R1

Factors affecting uptake of the levonorgestrel-releasing intrauterine device: A mixed-method study of social franchise clients in Nigeria

Dear Dr. Rademacher:

I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department.

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on behalf of

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Academic Editor

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Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Supplementary Materials

    Attachment

    Submitted filename: Responses_reviewers.docx

    Data Availability Statement

    The de-identified survey dataset, the survey questionnaire, and the in-depth interview guide are publicly available online through the Harvard Dataverse (https://dataverse.harvard.edu/dataverse/fhi360_leap). Full qualitative transcripts are not available for ethical reasons because of the risk of deductive disclosure. However, relevant excerpts of transcripts are available from the authors on reasonable request.


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