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NCT04307641 Clinical Trial

Improving Person Centered Care for Abortion Clients in India

Reproductive Health Clinical Trial

— SPARQ_ACI  

Official title:
Strengthening Patient-Centered Accessibility, Respect, and Quality of Care for Abortion Clients in UP, India

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04307641
Other study ID # 15-18008_India Abortion
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 1, 2016
Est. completion date July 1, 2018

Study information
Verified date March 2020
Source University of California, San Francisco
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to understand the effect of providing pharmacists in UP, India with additional information about medication abortion.

Description:

This study evaluates whether providing pharmacists with additional information about medication abortion can improve abortion person-centered care for women accessing MA at these sites.

Recruitment information / eligibility
Status Completed
Enrollment 283
Est. completion date July 1, 2018
Est. primary completion date July 1, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Pharmacist providing medication abortion within Lucknow, Kanpur, Unnao - Agreed to participate Exclusion Criteria: - Pharmacists not providing medication abortion within Lucknow, Kanpur, Unnao - Did not agree to participate

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• 2 Page Information Sheet
2 page information sheet about medication abortion

Locations
Country Name City State
n/a

Sponsors (2)
Lead Sponsor Collaborator
University of California, San Francisco Public Health Foundation of India

Outcome
Type Measure Description Time frame Safety issue
Primary Change in knowledge about medication abortion self-reported survey (dose, time, side effects, complications) baseline compared to 6-months after intervention
Secondary Provider behavior when providing medication abortion (MA) to clients Information provided to mystery clients regarding MA (dose, time, side effects, complications) 3-months post intervention
Secondary Interest and satisfaction with intervention self-reported survey on interest and satisfaction 6-months after intervention
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