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

Sponsor
University of California, San Francisco (Other)
Overall Status
Completed
CT.gov ID
NCT04208191
Collaborator
Innovations for Poverty Action (Other)
3,354
1
4
32.1
104.5

Study Details

Study Description

Brief Summary

Evaluation of a quality improvement (QI) collaborative aimed at improving person-centered care (PCC) for maternal health (MH) and family planning (FP) services

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Quality Improvement Collaborative
N/A

Detailed 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.

Study Design

Study Type:
Interventional
Actual Enrollment :
3354 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Strengthening People-centered Accessibility, Respect, and Quality for Maternal Health and Family Planning Services in Nairobi, Kenya
Actual Study Start Date :
Aug 8, 2016
Actual Primary Completion Date :
Apr 12, 2019
Actual Study Completion Date :
Apr 12, 2019

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Control - Women

Participants who delivered or received family planning services at a facility that was not implementing a QI project on PCC

Experimental: Intervention - Women

Participants who delivered or received family planning services at a facility that was implementing a QI project on PCC

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

No Intervention: Control - Provider

Provider working in a facility that is not implementing a QI project on PCC

Experimental: Intervention - Provider

Provider working in a facility that is implementing a QI project on PCC

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

Outcome Measures

Primary Outcome Measures

  1. Person Centered Maternal Health Scale Score [Baseline]

    Survey conducted with women: self report of experiences of care. Possible range 0-100; higher the score the better the experience of care

  2. Person Centered Maternal Health Scale Score [2-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

  3. Person Centered Maternal Health Scale Score [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

  4. Person Centered Maternal Health Scale Score [6-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

  5. Person Centered Maternal Health Scale Score [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

  6. Person Centered Maternal Health Scale Score [About 24 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

  7. Person Centered Maternal Health Scale Score [About 26 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

  8. Person Centered Maternal Health Scale Score [About 30 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

  9. Person Centered Maternal Health Scale Score [About 30.5 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

  10. Person Centered Maternal Health Scale Score [about 31 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

  11. Person Centered Maternal Health Scale Score [31.5 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

  12. Person Centered Maternal Health Scale Score [32 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

  13. Person Centered Maternal Health Scale Score [32.5 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

  14. Person Centered Family Planning Scale Score [Baseline]

    Survey conducted with women: self report of experiences of care. Possible range 0-43; higher the score the better the experience of care

  15. Person Centered Family Planning Scale Score [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

  16. Person Centered Family Planning Scale Score [6 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

  17. Person Centered Family Planning Scale Score [8 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

  18. Person Centered Family Planning Scale Score [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

  19. Person Centered Family Planning Scale Score [About 24 months 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

  20. Person Centered Family Planning Scale Score [About 26 months 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

  21. Person Centered Family Planning Scale Score [About 30 months 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

  22. Person Centered Family Planning Scale Score [About 31 months 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

  23. Person Centered Family Planning Scale Score [About 31.5 months 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

  24. Person Centered Family Planning Scale Score [About 32 months 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

  25. Person Centered Family Planning Scale Score [About 32.5 months 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

  26. Attitudes toward Person-Centered Care [Baseline]

    Survey and In-depth interviews conducted with providers; perceptions of person-centered care

  27. Attitudes toward Person-Centered Care [About 24 months post baseline]

    Survey conducted with providers; perceptions of person-centered care

  28. Attitudes toward Person-Centered Care [About 26 months post baseline]

    Survey conducted with providers; perceptions of person-centered care

  29. Attitudes toward Person-Centered Care [About 30 months post baseline]

    Survey and In-depth interviews conducted with providers; perceptions of person-centered care

  30. The Model for Understanding Success in Quality Survey [About 30 months post baseline]

    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

Eligibility Criteria

Criteria

Ages Eligible for Study:
15 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Innovations for Poverty Action Nairobi Kenya

Sponsors and Collaborators

  • University of California, San Francisco
  • Innovations for Poverty Action

Investigators

  • Principal Investigator: Dominic Montagu, DrPH, University of California, San Francisco

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of California, San Francisco
ClinicalTrials.gov Identifier:
NCT04208191
Other Study ID Numbers:
  • 15-18008_KenyaQI
First Posted:
Dec 23, 2019
Last Update Posted:
Dec 23, 2019
Last Verified:
Dec 1, 2019
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University of California, San Francisco

Study Results

No Results Posted as of Dec 23, 2019