Quality Improvement Project for Maternal Health and Family Planning Services in Kenya

Maternal Health Clinical Trial

— SPARQ_QIK  

Official title:

Strengthening People-centered Accessibility, Respect, and Quality for Maternal Health and Family Planning Services in Nairobi, Kenya

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04208191
• Other study ID #: 15-18008_KenyaQI
• Status: Completed
• Phase: N/A
• Start date: August 8, 2016
• Est. completion date: April 12, 2019

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 maternal health (MH) and family planning (FP) services

Description:

Evaluation of a quality improvement (QI) collaborative in public facilities in Nairobi and Kiambu Counties in Kenya aimed at improving person-centered care (PCC) for maternal health (MH) and family planning (FP) services.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 3354
• Est. completion date: April 12, 2019
• Est. primary completion date: April 12, 2019
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 15 Years and older

Eligibility

Inclusion Criteria for Women:

• Women aged 15-49 years old

• Agreed/consented to participate

• Delivered at the facility within the last 7 days OR adopted a family planning method at their visit on day of survey

• Has a working mobile phone and specified service provider (airtel/safaricom)

Exclusion Criteria for Women:

• Not a women aged 15-49 years old

• Did no agreed/consented to participate

• Did not deliver at the facility within the last 7 days OR adopted a family planning method at their visit on day of survey

• Does not have a working mobile phone or specified service provider (airtel/safaricom)

Inclusion Criteria for Providers:

• Agreed/consented to participate

• Staff at facility

Exclusion Criteria for Providers

• Did no agreed/consent to participate

• Not staff at facility

Related Conditions & MeSH terms

• Delivery
• Family Planning
• Maternal Health

Intervention

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

Locations

Country	Name	City	State
Kenya	Innovations for Poverty Action	Nairobi

Sponsors (2)

Lead Sponsor	Collaborator
University of California, San Francisco	Innovations for Poverty Action

Country where clinical trial is conducted

Kenya, 

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 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	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	6-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 24 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 26 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 30 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 30.5 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	about 31 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	31.5 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	32 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	32.5 months 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	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	6 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	8 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	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	About 24 months 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	About 26 months 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	About 30 months 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	About 31 months 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	About 31.5 months 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	About 32 months 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	About 32.5 months post baseline
Primary	Attitudes toward Person-Centered Care	Survey and In-depth interviews conducted with providers; perceptions of person-centered care	Baseline
Primary	Attitudes toward Person-Centered Care	Survey conducted with providers; perceptions of person-centered care	About 24 months post baseline
Primary	Attitudes toward Person-Centered Care	Survey conducted with providers; perceptions of person-centered care	About 26 months post baseline
Primary	Attitudes toward Person-Centered Care	Survey and In-depth interviews conducted with providers; perceptions of person-centered care	About 30 months post baseline
Primary	The Model for Understanding Success in Quality Survey	Survey conducted with intervention providers on facility readiness to implement QI; Possible range 0-154; higher the score the more ready facility is to participate in QI activities	About 30 months post baseline