Quality Improvement Project for Reproductive Health Services in India, Phase 1

Maternal Health Clinical Trial

— SPARQ_QII1  

Official title:

Strengthening People-centered Accessibility, Respect, and Quality for Reproductive Health Services in Uttar Pradesh, India, Phase 1

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04208867
• Other study ID #: 15-18008_IndiaQI1
• Status: Completed
• Phase: N/A
• Start date: September 16, 2016
• Est. completion date: December 6, 2018

Study information

• Verified date: December 2019
• Source: University of California, San Francisco
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Evaluation of a quality improvement (QI) collaborative aimed at improving person-centered care (PCC) for reproductive health (RH) services.

Description:

Evaluation of a quality improvement (QI) collaborative in public facilities in Uttar Pradesh, India aimed at improving person-centered care (PCC) for reproductive health (RH) services.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 2989
• Est. completion date: December 6, 2018
• Est. primary completion date: December 6, 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria for Women:

• Women aged 18-49

• Agree/consent to participate

• Delivered a baby at the facility within 7 days (or adopted a family planning method at time of visit (baseline only, not part of intervention))

Exclusion Criteria for Women:

• Not a women aged 18-49

• Did not agree/consent to participate

• Did not deliver a baby at the facility within 7 days (or adopted a family planning method at time of visit (baseline only, not part of intervention))

Inclusion Criteria for Providers:

• Agreed/consented to participate

• Staff at facility

Exclusion Criteria for Provider:

• Did not agree/consent to participate

• Not Staff at facility

Related Conditions & MeSH terms

• Delivery
• Maternal Health
• Reproductive Health

Intervention

Behavioral:
• QI Collaborative
Facilities that participated in a QI collaborative to improve PCC for MH services

Locations

Country	Name	City	State
India	Population Services International	Lucknow	Uttar Pradesh

Sponsors (2)

Lead Sponsor	Collaborator
University of California, San Francisco	Population Services International

Country where clinical trial is conducted

India, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Person Centered Maternal Health Scale Score	Survey conducted with women: self report of experiences of care. Possible range 0-100; higher the score the better the experience of care	Baseline
Primary	Person Centered Maternal Health Scale Score	Survey conducted with women: self report of experiences of care. Possible range 0-100; higher the score the better the experience of care	2-weeks post basline
Primary	Person Centered Maternal Health Scale Score	Survey conducted with women: self report of experiences of care. Possible range 0-100; higher the score the better the experience of care	4 weeks post baseline
Primary	Person Centered Maternal Health Scale Score	Survey conducted with women: self report of experiences of care. Possible range 0-100; higher the score the better the experience of care	10 weeks post baseline
Primary	Person Centered Maternal Health Scale Score	Survey conducted with women: self report of experiences of care. Possible range 0-100; higher the score the better the experience of care	About 12 months post baseline
Primary	Person Centered Maternal Health Scale Score	Survey conducted with women: self report of experiences of care. Possible range 0-100; higher the score the better the experience of care	About 14 months post baseline
Primary	Person Centered Maternal Health Scale Score	Survey conducted with women: self report of experiences of care. Possible range 0-100; higher the score the better the experience of care	about 24 months after baseline
Primary	Person Centered Maternal Health Scale Score	Survey conducted with women: self report of experiences of care. Possible range 0-100; higher the score the better the experience of care	About 24.5 months post baseline
Primary	Person Centered Maternal Health Scale Score	Survey conducted with women: self report of experiences of care. Possible range 0-100; higher the score the better the experience of care	25 months post baseline
Primary	Person Centered Maternal Health Scale Score	Survey conducted with women: self report of experiences of care. Possible range 0-100; higher the score the better the experience of care	26.5 months past baseline
Primary	Person Centered Family Planning Scale Score	Survey conducted with women: self report of experiences of care. Possible range 0-43; higher the score the better the experience of care	Baseline
Primary	Person Centered Family Planning Scale Score	Survey conducted with women: self report of experiences of care. Possible range 0-43; higher the score the better the experience of care	4 weeks post baseline
Primary	Person Centered Family Planning Scale Score	Survey conducted with women: self report of experiences of care. Possible range 0-43; higher the score the better the experience of care	10 weeks post baseline
Primary	Attitude toward Person-Centered Care	Survey and in-depth interviews conducted with providers; perceptions of person-centered care	About 12 months post baseline
Primary	Attitude toward Person-Centered Care	Survey and in-depth interviews conducted with providers; perceptions of person-centered care	About 24 months post baseline