Clinical trial Recruiting at 2 sites Interventional Ages 18 and up Women only

Telemedicine for contraceptive counseling compared to standard care

Official title: Telemedicine Contraceptive Counselling (TECC) Versus Standard Care - a Pilot and Randomized Controlled Trial of Periabortion Contraceptive Counseling

Run by Karolinska Institutet · NCT06682065 · Data updated 2026-11-12

This study is testing a new telemedicine service for contraceptive counseling to see if it helps more people in South Africa and Kenya choose long-acting birth control after an abortion compared to regular in-person counseling.

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Quick facts

Study typeInterventional
Ages18 Years and up
SexWomen only
Enrollment510 (estimated)
SponsorKarolinska Institutet
Academic / other
Locations2 sites (Cape Town and 1 other locations)
StatusRecruiting
StartedMay 5, 2024
Main results expectedFebruary 15, 2025
Study endsFebruary 15, 2026
Registry record updatedNovember 12, 2024
Trial IDNCT06682065 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are women aged 18 and older who are seeking either medical or surgical abortion and have access to a smartphone.

Probably not a fit

Patients who do not have access to a smartphone or are unable to communicate in English may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This project aims to enhance access to contraception following abortion by developing and testing a telemedicine service for contraceptive counseling (TECC). It includes a pilot study and a multicenter randomized controlled trial in South Africa and Kenya. The study will evaluate the effectiveness of TECC in increasing the uptake of long-acting reversible contraception (LARC) compared to traditional in-person counseling. Additionally, it will assess user satisfaction, preferences, and rates of unintended pregnancies and abortions following the counseling.

Why it matters

Potential benefit: If successful, this approach could significantly improve access to contraceptive options for women post-abortion, potentially reducing rates of unintended pregnancies.

How similar studies have gone: Other studies have shown promising results with telemedicine approaches in healthcare, suggesting potential success for this novel intervention.

Who can join: the full rules

Show full inclusion / exclusion criteria
* Seeking either surgical or medical abortion
* ≥ 18 years of age
* Able to communicate and understand spoken and written English
* With private access to a smart phone
* Willing to participate in the study procedures

Where it's running

  • Michael Mapongwana
    Cape Town, South Africa
    Recruiting
  • Mitchell´s Plain CHC
    Cape Town, South Africa
    Recruiting

Study contacts

  • Principal investigator: Margit Endler, PhD — Karolinska Institutet
  • Study coordinator: Margit Endler
  • Email: margit.endler@ki.se
  • Phone: 0789106286

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.