ClinicalTrials.gg
RecruitingNCT07527364Updated May 11, 2026

Evaluation of Changing the Scripts Intervention in Nigeria

An interventional study of Multimedia (BBC MA) intervention: Changing the Script in Nigeria and Supply-side interventions (MSI) in Unintended Pregnancy Prevention, sponsored by University of California, San Diego. Recruiting at 3 sites in Nigeria. Open to female participants aged 15 Years to 44 Years. Per ClinicalTrials.gov, last updated 2026-05-11.

Sponsored by University of California, San Diego · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Started Apr 2026; still recruiting 6 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
4,000
Allocation
Non-randomized
Ages
15 Years to 44 Years
Sex
Female
01

Study summary

The Center on Gender Equity and Health is evaluating a multimedia social and behavior change (SBC) intervention in Kano and Kaduna states in Nigeria to assess its impact, cost-efficiency and how it works. The intervention, led by BBC Media Action, uses radio, TV, other media, community outreach and SBC approaches to increase women's and couples' ability to make and act on reproductive and family planning decisions. Over a three-year period (2025- 2028), we will use a mixed-methods prospective longitudinal cohort study design to meet the research objectives. This includes estimating the impact of the intervention on use and intent to use modern contraception (alone, when combined with other family planning programs, and among non-users), exploring the pathways through which the intervention increases contraceptive use, estimating the cost-efficiency of the intervention and, evaluating the sustainability of the intervention. Data will be collected from three states - Kano and Kaduna (intervention states) and Nasarawa (comparison state). Through this evaluation, we aim to contribute to the family planning and mass media SBC fields by strengthening the evidence on the impact of a multimedia SBC intervention as well as the additional impact of combining the intervention with family planning service delivery interventions.

Read the detailed description

Background: Modern contraception use to space or limit births is an important aspect of reproductive health because it has the potential to improve maternal health and child outcomes, reduce poverty, and promote gender equality. Despite their benefits, modern contraceptive use remains low in many developing countries, including Nigeria. Nigeria has the largest population and one of the lowest modern contraceptive use rates in sub-Saharan Africa. The 2023-2024 Nigerian Demographic and Health Survey (NDHS) found that the prevalence of modern contraceptives among married women was 15.3%, a 3-percentage point increase from the 2018 NDHS. Rates in Kano and Kaduna continue to remain lower than the national average. In Kano, about 10.6% of married women were using a modern method, roughly double the level recorded in the 2018 NDHS, while in Kaduna, a slight decrease was observed (0.6%) over the years and by 2023-2024 survey about 13.1% were using a modern contraceptive method.

Mass media interventions have been used over the years to address low family planning uptake because they can simultaneously influence individuals, families, peer networks and communities. Evidence across these different ecological levels have found that mass media approaches can influence family planning behaviors, knowledge, perceptions, attitudes and expectations . However, despite the large body of evidence documenting the impact of mass media, there's a need for rigorous evaluations that measure multiple outcomes along the behavioral pathway as well as assessments that capture the cost implications.

Objective: The objective of this study is to evaluate a multimedia intervention to be implemented by BBC Media Action in Kano and Kaduna. This evaluation will estimate the intervention's impact on family planning/child spacing method use, examine behavioral mechanisms of change, estimate cost-efficiency, and generate insights into its sustainability.

Methodology: Using a quasi-experimental design, the evaluation will be conducted in Kano, Kaduna, and Nasarawa (comparison) States. It is a three-year (2026 - 2028), mixed-methods, longitudinal evaluation of the BBC Media Action multimedia SBC intervention. Data collected will include a longitudinal cohort survey with women of reproductive age who meet our inclusion criteria at baseline. The baseline survey will be collected before the intervention begins and a follow-up survey will be conducted two years after the start of intervention implementation. In addition, in-depth interviews will be conducted with a subset of the cohort women and their partners, and program monitoring interviews with intervention women, intervention men, and program implementers. Key informant interviews and an online survey will be conducted with key implementing partners to gather insights into sustainability. To inform the cost efficiency analysis, costs associated with implementation will be collected from the financial management systems of partners along with semi-structured interviews with partners.

02

Conditions studied

  • Unintended Pregnancy Prevention

Keywords

  • Contraceptive Use
  • Family Planning
  • Child Spacing
  • Multimedia Evaluation
  • Social and Behavior Change
03

In context

Lead sponsor

University of California, San Diego is the lead sponsor of 980 studies on the registry; 195 are open to participants now.

Of its 113 completed or terminated interventional studies of FDA-regulated products, 71 (63%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
15 Years to 44 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

All eligibility criteria based on self-report:

  • Aged 15-44 years old at baseline
  • Female
  • Sexually active (based on self-report; i.e., in union)
  • Able to provide
  • Current residence in the selected intervention or comparison area

Exclusion criteria

Exclusion Criteria:

  • Are not considered sexually active (i.e. not in union)
  • Are unable to provide consent
  • Are younger than 15 years and older than 44 years at baseline
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
4,000 participants (estimated)

Study arms

  • Experimental
    Arm 1: Multimedia (BBC MA) + Supply Side Interventions (MSI)

    Arm 1 includes local government areas (LGAs) in Kano and Kaduna that will receive the multimedia intervention led by BBC Media Action (BBC MA) and have existing Marie Stopes International (MSI) supply-side interventions

    Behavioral: Multimedia (BBC MA) intervention: Changing the Script in Nigeria · Other: Supply-side interventions (MSI)

  • Experimental
    Arm 2: Multimedia intervention (BBC MA) only

    Arm 2 includes LGAs in Kano and Kaduna that will only receive the BBC MA multimedia intervention but do NOT have existing MSI supply-side interventions.

    Behavioral: Multimedia (BBC MA) intervention: Changing the Script in Nigeria

  • Active comparator
    Arm 3: Supply Side Interventions (MSI) only

    Arm 3 includes LGAs in Nasarawa that have existing MSI supply side interventions but will NOT receive the multimedia (BBC MA) intervention

    Other: Supply-side interventions (MSI)

Interventions

  • BehavioralMultimedia (BBC MA) intervention: Changing the Script in Nigeria

    Led BBC Media Action (BBC MA) and implemented in collaboration with multiple partners, the intervention will create an integrated "story world" designed to shift knowledge, attitudes, and beliefs, spark conversations, and reshape social norms around family planning or child spacing. The aim is to empower women and couples to make and act on informed family planning/child spacing decisions, ultimately increasing uptake and continuation of contraception. This will be achieved through a range of multimedia channels and formats, including TV drama, radio drama, radio discussion and call-in shows, public service announcements, social media, mobile IVR drama, and community engagement.

  • OtherSupply-side interventions (MSI)

    Family planning services in the public sector in Nigeria supported by supply-side interventions implemented by Marie Stopes International (MSI) Nigeria. Supply-side interventions include health provider training on family planning service provision, supporting family planning commodity supply, and monitoring family planning service quality.

06

What researchers measure

Primary outcomes

  1. Current family planning use

    Change in prevalence of women's self-reported FP use (1) any FP method; 2) modern FP method) between baseline and 2-year follow-up in each intervention group compared to the comparison group (difference-in-differences)

    Time frame: Baseline and follow-up (2 years after implementation start)

  2. Intent to use a family planning method

    Change in prevalence of women's self-reported intent to use an FP method between baseline and 2-year follow-up in each intervention group compared to the comparison group (difference-in-differences). This will be a categorical variable measured among all participants, defined as 0=No intent, 1=Intent, 2=FP User. Intent to use FP will be assessed in the following scenarios: 1. At any time in the future 2. In the next 12 months/within 12 months of giving birth (for pregnant women) 3. After the birth of the next child to delay a subsequent pregnancy 4. After the birth of the next child to allow for rest before another pregnancy 5. Once ideal family size is reached 6. If she needs to avoid or delay a pregnancy for health reasons

    Time frame: Baseline and follow-up (2 years after implementation start)

  3. Favorable attitude towards family planning

    Change in prevalence of women reporting that they are in favor of the use of family planning/child spacing methods between baseline and 2-year follow-up in each intervention group compared to the comparison group (difference-in-differences)

    Time frame: Baseline and follow-up (2 years after implementation start)

Secondary outcomes

  1. Confidence in ability to use family planning

    Change in prevalence of women reporting that they feel confident they could use FP if they wanted to between baseline and 2-year follow-up in each intervention group compared to the comparison group (difference-in-differences)

    Time frame: Baseline and follow-up (2 years after implementation start)

  2. Self-efficacy to discuss family planning/child spacing with partner/husband

    Change in women's mean self-efficacy score (CSESSA Nigeria husband/partner communication sub-scale) between baseline and 2-year follow-up in each intervention group compared to the comparison group (difference-in differences). Range: 0-40 with higher values indicating higher levels of self-efficacy.

    Time frame: Baseline and follow-up (2 years after implementation start)

  3. Frequency of communication about family planning/child spacing with husband/partner

    Change in prevalence of women reporting that they communicate about family planning/child spacing methods with their husband/partner "often" or "sometimes" between baseline and 2-year follow-up in each intervention group compared to the comparison group (difference-in-differences)

    Time frame: Baseline and follow-up (2 years after implementation start)

  4. Perceived prevalence of family planning use

    Change in mean number of married women in the community (out of 10) that participants think use family planning/child spacing methods between baseline and 2-year follow-up in each intervention group compared to the comparison group (difference-in-differences). Range: 0-10 with higher values indicating a higher perceived prevalence of FP use among married women in their community.

    Time frame: Baseline and follow-up (2 years after implementation start)

  5. Concrete plan to use family planning

    Change in prevalence of women reporting that they have a concrete plan to start using an FP method (including having identified a place to access the FP method) between baseline and 2-year follow-up in each intervention group compared to the comparison group (difference-in-differences)

    Time frame: Baseline and follow-up (2 years after implementation start)

  6. Preference-aligned fertility management (PFM)

    Change in prevalence of women whose fertility preferences align with their contraceptive behavior between baseline and 2-year follow-up in each intervention group compared to the comparison group (difference-in-differences). PFM is defined as: 1. Currently using an FP method (always or sometimes) + Desiring to use that FP method OR 2. Currently not using an FP method + Do not desire to use an FP method

    Time frame: Baseline and follow-up (2 years after implementation start)

  7. Family planning intent actualized

    Change in prevalence of women reporting FP use (1) any FP method or 2) modern FP method) any time within the 2-year follow-up period among those who reported intending to use an FP method at baseline between each intervention group compared to the comparison group at the 2-year follow-up (single time point)

    Time frame: Follow-up (2 years after implementation start)

07

Study locations

3 of 3 sites recruiting
  • Household survey
    Kaduna, Nigeria
    Recruiting
  • Household survey
    Kano, Nigeria
    Recruiting
  • Household survey
    Nasarawa, Nigeria
    Recruiting
08

References and documents

Publications

  • National Population Commission - NPC, & ICF. (2019). Nigeria Demographic and Health Survey 2018 - Final Report. http://dhsprogram.com/pubs/pdf/FR359/FR359.pdf
  • High Impact Practices in Family Planning (HIPs). (2017). Mass Media: Reaching audiences far and wide with messages to support healthy reproductive behaviors. https://fphighimpactpractices.org/briefs/mass-media
  • Federal Ministry of Health Social Welfare of Nigeria (FMoHSW), National Population Commission - NPC/Nigeria, & ICF. (2025). Nigeria Demographic and Health Survey 2024. https://www.dhsprogram.com/pubs/pdf/FR395/FR395.pdf
  • Dasgupta, A., Kantorová, V., Ueffing, P., & Wheldon, M. (2022). Contraceptive use and fertility transitions: The distinctive experience of sub-Saharan Africa. Demographic Research, 46(4), 97-130. https://doi.org/10.4054/DemRes.2022.46.4

Individual participant data

Plan to share: Yes — The de-identified participant data analysis sets will be uploaded to a public data repository upon publication of findings

Supporting information: Study protocol, Statistical analysis plan, Informed consent form, Analytic code

Time frame: Upon publication of findings

Access criteria: Open Access

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Apr 2026 (actual). Primary completion is estimated for May 2028, 25 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Apr 7, 2026
First posted
Apr 14, 2026
StartActual
Apr 13, 2026
Primary completionEst.
May 30, 2028
CompletionEst.
Oct 31, 2028
Last update
May 11, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on May 11, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07527364
Collaborators
Oxford Policy Management
Responsible party
Erin Pearson (Director of Global Partnerships and Collaborative Learning, Center on Gender Equity and Health, University of California, San Diego) — Principal investigator
First posted
Apr 14, 2026
Start date
Apr 13, 2026
Primary completion
May 30, 2028 (estimated)
Completion
Oct 31, 2028 (estimated)
Last update
May 11, 2026

Study contacts

Francine E Wood, PhD, MPH
Contact
fwood@health.ucsd.edu
+1-424-209-9188
Erin Pearson, PhD, MPH
Contact
eepearson@health.ucsd.edu
1-254-624-6937
Erin Pearson, PhD, MPH
principal investigator · University of California, San Diego

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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