Evaluating the HOPE Intervention to Increase Cervical Cancer Screening Among Women Living with HIV in Ghana Using a Hybrid Effectiveness and Implementation Trial
Led by Baylor University · Updated on 2026-07-01
1500
Participants Needed
1
Research Sites
25 weeks
Total Duration
AI-Summary
What this Trial Is About
Researchers are evaluating the HOPE intervention, a home-based self-sampling and education program aimed at increasing cervical cancer screening among women living with HIV WLWH in Ghana. This study addresses the low screening rates in this high-risk group by developing and testing implementation strategies to integrate HOPE into existing healthcare practices. The trial uses a hybrid type 2 effectiveness-implementation randomized controlled design to improve screening uptake and sustainment within the health system.
The study involves four secondary-level HIV clinics in Ghana, which are cluster-randomized into two groups. In the intervention group, healthcare providers receive training and implementation support strategies ISS including management support, capacity-building, and social network support to help deliver the HOPE 2.0 program. The control group providers implement HOPE without receiving ISS or training. The trial includes phases for preparation, implementation, and sustainment, focusing on adapting strategies and assessing their impact on screening behaviors and provider confidence.
Participants include women living with HIV aged 25 to 65 who have not undergone cervical cancer screening in the past five years and healthcare providers at the study sites. The study collects data on program adoption, implementation costs, fidelity, penetration, and sustainment over periods ranging up to 42 months post-randomization. Researchers will also measure provider self-efficacy, patient screening uptake, follow-up treatment, and patient satisfaction. Participation involves recruitment by trained providers, delivery of the intervention, and follow-up assessments to evaluate outcomes and sustainment.
CONDITIONS
Brief Title
Home-based Self-sampling for Cervical Cancer Prevention Education Intervention in Ghana
Research Team
M
Matthew Asare, PhD
D
Dorcas Obiri-Yeboah, PhD
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match. Sign up to get personalized trial recommendations delivered to your inbox.
Able to give consent according to Institutional Review Board rules
Residing in the Central Region of Ghana
No medical conditions that would prevent full participation
Willingness to participate in the study
Healthcare providers aged 18 or older working at HIV health facilities (no gender restriction)
Women living with HIV identified female at birth, aged 25 to 65
Women who have never had cervical cancer screening or have not been screened in the past 5 years
You will not qualify if you...
Women who are pregnant
Women who have had a hysterectomy
Women below 25 years or above 65 years of age
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Implementation and Intervention
Duration - Up to 42 months post-randomization
Healthcare providers in selected clinics receive training and implementation support to deliver the HOPE program. Providers recruit women living with HIV to participate and apply the home-based self-sampling and education intervention. Control group providers implement HOPE without extra support.
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
Similar Trials
Improving HIV Testing in European Hospitals by Introducing Dedicated HIV Teams A Multicenter Study Across Ten Countries
Pilot Study of 1MoreStep A Behavioral Program to Improve HIV Care and Reduce Partner Violence in Black Women Living With HIV
Remote Community Health Worker-Delivered Counseling via mHealth to Reduce Anxiety and Depression in Adults With HIV
Pilot Study to Prevent Frailty in People Living with HIV Aged 65 to 74
Remote Tai ChiQigong Classes to Reduce Depression in Older Adults Living with HIV
Community Screening Study to Reduce Chlamydia and Other STIs in Black Youth Ages 15 to 26 in Orleans Parish
Phase 1 Trial to Assess Safety and Drug Levels of ePGT121v1-LS, PGDM1400LS, and VRC07-523LS
Given by IV or SC to Adults Without HIV-1 Aged 18 to 55
Randomized Trial to Improve Muscle Health and Reduce Fat in Veterans with HIV and Obesity
Phase 1 Study of GRAdHIVNE1 Vaccine for Adults With and Without HIV in Southern Africa
Phase 1 Study of DV700P-RNA and DV701B1.1-RNA Vaccines with Planned Antiretroviral Therapy Pause in Adults Living with HIV
Have more questions? Get in touch with our team for quick support
Published Research Related To This Trial
HOme-based self-sampling for cervical cancer prevention education among women living with HIV in Ghana (HOPE-inG): study protocol for a cluster-randomized type 2 hybrid effectiveness implementation trial.
Matthew Asare, Nadia Adjoa Sam-Agudu, Obed Cudjoe...