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Use of Low Sensitivity Pregnancy Test for Self-assessment of Medical Abortion

Not Applicable
Completed
Conditions
Completion of Medical Abortion
Interventions
Behavioral: Baseline verbal instruction on LSUPT
Registration Number
NCT02231619
Lead Sponsor
University of Cape Town
Brief Summary

The purpose of the study is to design a self-assessment package that could be the preferred option to a follow-up visit at the clinic by the majority of women having early medical abortion.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
525
Inclusion Criteria
  1. Already be signed up to do a medical abortion at this clinic
  2. Be willing to come to all clinic appointments and be accessible by phone for 2 weeks after sign up for the study
  3. Own a cellphone to which will be sent medical abortion-related information and messaging.
Exclusion Criteria
  1. Be doing a medical abortion due to failed natural miscarriage 2. Not have a working cellphone

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Baseline verbal instruction of LSUPTBaseline verbal instruction on LSUPTVerbal instruction on how to do LSUPT at baseline
Primary Outcome Measures
NameTimeMethod
Accurate self-assessment of medical abortion using a low sensitivity pregnancy test12 months

Participants will be randomized to 2 groups. Women in Group A will conduct a baseline low sensitivity urine pregnancy test (LSUPT) on their own urine specimen at their clinic visit with help from the fieldworker. Group B will receive a standardized set of verbal instructions on how to do the test. Both groups will do a LSUPT at home on Day 12.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Nolungile Youth Clinic, Khayelitsha

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Cape Town, Western Province, South Africa

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