ClinicalTrials.gg
Active, not recruitingNCT07756528Updated Aug 10, 2026

Stakeholder-Informed RSV Prevention Economic Model in Botswana

An observational study in RSV, sponsored by University of California, San Diego. Active, not recruiting at 1 site in Botswana. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-10.

Sponsored by University of California, San Diego · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
40
Ages
18 Years and older
Sex
All
01

Study summary

The goal of this mixed methods study is to engage stakeholders to develop a health economic model to estimate the costs, health benefits, and value of respiratory syncytial virus (RSV) prevention strategies. The model will help decision-makers in Botswana determine whether and how to introduce RSV prevention interventions for infants, including monoclonal antibodies.

The main questions the study aims to answer are:

How could RSV prevention strategies be delivered to infants in Botswana?

What costs, health benefits, and implementation factors should be included in a health economic model?

What information do policymakers, healthcare providers, funders, researchers, and other stakeholders need to make decisions about RSV prevention?

Participants will include key stakeholders involved in health policy, clinical care, financing, research, and child health in Botswana. Participants may be asked to complete an interview, take part in a stakeholder workshop, complete a survey, and help review or interpret model findings. The study will not test an RSV product in infants or provide medical treatment.

Read the detailed description

This mixed-methods observational study will develop a stakeholder-informed health economic model to evaluate potential respiratory syncytial virus (RSV) prevention strategies for infants in Botswana, including RSV monoclonal antibodies. The study will not administer an RSV prevention product to infants or assign participants to a medical intervention.

The study will engage policymakers, healthcare providers, funders, researchers, and patient representatives to identify the information needed to support decision-making about RSV prevention in Botswana. Study activities will include stakeholder advisory group meetings, semi-structured interviews, a structured stakeholder workshop, surveys, and model review activities.

Stakeholder input will be used to define key features of the health economic model, including target populations, delivery settings, implementation strategies, time horizon, costs, health outcomes, equity considerations, and uncertainty analyses. The model will estimate the potential cost-effectiveness and budget impact of RSV monoclonal antibody implementation among infants in Botswana, including strategies for all eligible infants and for higher-risk groups such as infants born preterm, infants exposed to HIV, and infants born during RSV season.

The study will also evaluate the stakeholder engagement process. Stakeholder advisory group members will be asked about their experiences participating in model development and their perceptions of whether the final model is relevant, usable, credible, and helpful for country-level decision-making. Findings will be used to refine the model and develop materials to support future stakeholder-engaged health economic modeling in Botswana and similar settings.

02

Conditions studied

  • RSV

Keywords

  • Respiratory syncytial virus
  • RSV monoclonal antibody
  • Health economic model
  • Budget impact
  • Cost-effectiveness
  • Stakeholder engagement
  • Decision analysis
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
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

We will establish a 20-member stakeholder advisory board representing policymakers (n=5), funders (n=3), healthcare providers (n=5), researchers (n=2), and leaders representing patient groups (n=5).

Eligibility criteria

Inclusion Criteria

  1. Expertise or Role:

    1. Policymakers: Currently employed in or recently retired from a government health agency, Ministry of Health, or other institution with responsibility for health policy, immunization, or maternal/child health.
    2. Funders: Employed by or affiliated with an organization that funds health services, immunization programs, or health research in Botswana or the region.
    3. Healthcare providers: Licensed clinicians (e.g., pediatricians, nurses, midwives) with direct experience delivering maternal or child health services in Botswana.
    4. Researchers: Active or recent experience in health economics, public health, or RSV-related research, with relevance to LMICs.
    5. Patient representatives: Affiliated with or leading a civil society or patient advocacy organization focused on child health, immunization, or health equity in Botswana.
  2. Geographic Relevance: Based in Botswana or with demonstrated experience working within Botswana's health system or policy landscape.
  3. Language: Comfortable speaking and reading English or Setswana.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
40 participants (estimated)
Patient registry
No

Groups and cohorts

  • Stakeholder group representing policymakers, healthcare providers, researchers, funders, an

    Up to 40 stakeholders will participate in an interview and up to 20 will participate in a workshop on health economic modeling and a pre/post survey.

06

What researchers measure

Primary outcomes

  1. Completion of a stakeholder-informed health economic model to evaluate RSV prevention strategies for infants in Botswana.

    Model completion will be measured as the number of pre-specified model development milestones completed. Milestones include: finalizing the model structure; identifying and documenting model input parameters; programming the model; conducting internal model checks; generating base-case results; conducting sensitivity analyses; reviewing model assumptions and preliminary results with stakeholders; and producing final model outputs for dissemination.

    Time frame: July 1, 2026 to December 30, 2027

Secondary outcomes

  1. Stakeholder-rated quality of engagement

    Stakeholder engagement will be assessed using a survey adapted from established engagement domains, including respect, trust, legitimacy, fairness, competence, and accountability. Participants involved in workshops and model-development activities will be asked to rate the extent to which the engagement process was inclusive, transparent, respectful, and useful for shaping the health economic model and its outputs.

    Time frame: July 1, 2026 to December 30, 2027

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Jul 2026 (actual). Primary completion is estimated for Oct 2027, 15 months after the start.

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

Registered
Aug 6, 2026
First posted
Aug 10, 2026
StartActual
Jul 1, 2026
Primary completionEst.
Oct 1, 2027
CompletionEst.
Dec 30, 2027
Last update
Aug 10, 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 Aug 10, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07756528
Collaborators
Botswana Harvard AIDS Institute Partnership
Responsible party
Adriane Wynn (Associate Professor, University of California, San Diego) — Principal investigator
First posted
Aug 10, 2026
Start date
Jul 1, 2026
Primary completion
Oct 1, 2027 (estimated)
Completion
Dec 30, 2027 (estimated)
Last update
Aug 10, 2026

Oversight

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

Not currently enrolling

This study is active, not recruiting, as verified in Jul 2026. You cannot join it, but the record below documents what was studied.

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