Clinical trial · Interventional
Leveraging Project ECHO for Improved Cervical Cancer Screening in Ethiopia
Leveraging Project ECHO for Improved Cervical Cancer Screening in Ethiopia: An Implementation Study of Integrated HPV Selfsampling in HIV Care Centers
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Project TICHILALECH ("she can" in Amharic), a five-year, implementation science study, is focused on improving cervical cancer screening, triage, and treatment and integration with human immunodeficiency virus (HIV) care at five Ethiopian hospitals, with a focus on human papillomavirus (HPV) self-collection as the recommended screening strategy for people living with HIV (PLHIV). To improve implementation of screening and treatment, Project ECHO (Extension for Community Healthcare Outcomes), a peer-based, virtual, knowledge sharing model, will be used to convene healthcare providers and stakeholders over a period of approximately three years (2026-2029). A customized curriculum is developed featuring didactic lectures, case-based presentations, and experience sharing for peer-mentoring. A pre/post study design will measure changes in delivery of clinical services, such as the proportion of HPV-positive patients that are appropriately triaged and treated, before and after each hospital's participation in the TICHILALECH ECHO intervention.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Cervical Carcinoma | Cervical Carcinoma | ONTOLOGY_EXACT | 0.98 |
| Human Papilloma Virus (HPV) | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| TICHILALECH ECHO | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Participation in TICHILALECH ECHO
- description
- Healthcare providers and relevant stakeholders participate in TICHILALECH ECHO, a peer-to-peer virtual learning modality.
- interventionNames
- Behavioral: TICHILALECH ECHO
Primary outcomes (2)
- measure
- Triage Examination Percentage Among Screen-Positive People Living with HIV (PLHIV)
- timeFrame
- Baseline: 12 months prior to TICHILALECH ECHO study intervention; Post: Up to 12 months following TICHILALECH ECHO study intervention
- description
- Percentage of screen-positive PLHIV who received at least one timely (i.e., within 6 months of a positive screening result) triage examination (i.e., HPV partial genotyping, colposcopy, visual inspection with acetic acid (VIA), or cytology), assessed separately for the baseline period (i.e., the 12 month period prior to ECHO intervention implementation) and the post-intervention period (i.e., 12 month period following ECHO intervention implementation)
- measure
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria for Project ECHO and associated surveys, interviews, and focus group discussions: * 18 years or older * Willingness and ability to provide informed consent and participate in virtual, peer-mentoring through Project ECHO * Profession: Healthcare provider, any education/training/cadre with experience relevant to the delivery of cervical cancer screening and treatment or HIV care (e.g., cervical cancer screening, gynecologist, gynecological oncologist, or HIV/ ART provider), or other stakeholder (e.g., personnel at laboratories or health bureaus, administrators, ART data clerks) * Can communicate in English or Amharic (national language of Ethiopia) * Able and willing to meaningfully contribute in the virtual, peer-learning community of Project ECHO Inclusion criteria for end service users (PLHIV) for focus group discussion and routine clinical service delivery data: * 25 years or older (in accordance with Ethiopia's national cervical cancer screening guidelines for PLHIV) * Have been diagnosed with HIV * Have a history of cervical cancer screening that was performed at one of the five study sites, either during the course of our study or previously * Were screened with primary HPV DNA testing during the course of the study intervention period * Are eligible for cervical cancer screening in accordance with Ethiopia's national cervical cancer screening guidelines (e.g., have an intact cervix) Exclusion criteria for end service users (PLHIV) for focus group discussion: * HIV negative status * Age under 25 years * Any physical or mental disability that prevents the individual from consenting to cervical cancer screening and/or study participation * Patients without an intact cervix (e.g. a history of hysterectomy) * Anyone ineligible for cervical cancer screening in accordance with Ethiopia's national cervical cancer screening guidelines Note: Routine clinical service delivery data of PLHIV will be reviewed to determine intervention effect of providers participating in Project ECHO. PLHIV are not considered participants of the trial and are not consented.
References
Publications (35)
- BACKGROUNDEthiopian Federal Ministry of Health. National Guideline for Cervical Cancer Prevention and Control Ethiopia. 2025.
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