Population Services International
Lucknow, Uttar Pradesh, India
NCT Number: NCT04208867
Evaluation of a quality improvement (QI) collaborative aimed at improving person-centered care (PCC) for reproductive health (RH) services.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Lucknow, Uttar Pradesh, India
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.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
for Women:
Exclusion criteria
for Women:
Inclusion criteria
for Providers:
Exclusion criteria
for Provider:
Facilities that participated in a QI collaborative to improve PCC for MH services
Time frame: Baseline
Survey conducted with women: self report of experiences of care. Possible range 0-100; higher the score the better the experience of care
Time frame: 2-weeks post basline
Survey conducted with women: self report of experiences of care. Possible range 0-100; higher the score the better the experience of care
Time frame: 4 weeks post baseline
Survey conducted with women: self report of experiences of care. Possible range 0-100; higher the score the better the experience of care
Time frame: 10 weeks post baseline
Survey conducted with women: self report of experiences of care. Possible range 0-100; higher the score the better the experience of care
Time frame: About 12 months post baseline
Survey conducted with women: self report of experiences of care. Possible range 0-100; higher the score the better the experience of care
Time frame: About 14 months post baseline
Survey conducted with women: self report of experiences of care. Possible range 0-100; higher the score the better the experience of care
Time frame: about 24 months after baseline
Survey conducted with women: self report of experiences of care. Possible range 0-100; higher the score the better the experience of care
Time frame: About 24.5 months post baseline
Survey conducted with women: self report of experiences of care. Possible range 0-100; higher the score the better the experience of care
Time frame: 25 months post baseline
Survey conducted with women: self report of experiences of care. Possible range 0-100; higher the score the better the experience of care
Time frame: 26.5 months past baseline
Survey conducted with women: self report of experiences of care. Possible range 0-100; higher the score the better the experience of care
Time frame: Baseline
Survey conducted with women: self report of experiences of care. Possible range 0-43; higher the score the better the experience of care
Time frame: 4 weeks post baseline
Survey conducted with women: self report of experiences of care. Possible range 0-43; higher the score the better the experience of care
Time frame: 10 weeks post baseline
Survey conducted with women: self report of experiences of care. Possible range 0-43; higher the score the better the experience of care
Time frame: About 12 months post baseline
Survey and in-depth interviews conducted with providers; perceptions of person-centered care
Time frame: About 24 months post baseline
Survey and in-depth interviews conducted with providers; perceptions of person-centered care
University of California, San Francisco
Other
Strengthening People-centered Accessibility, Respect, and Quality for Reproductive Health Services in Uttar Pradesh, India, Phase 1
Acronym: SPARQ_QII1
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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