Reproductive Health Clinical Trial
— SPARQ_PACKOfficial title:
Strengthening Patient-Centered Accessibility, Respect, and Quality of Care for Post Abortion Care Through Peer and Nurse Based Phone Support
Verified date | January 2020 |
Source | University of California, San Francisco |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to understand the effect of a phone based post-abortion intervention on the experience of post-abortion care.
Status | Completed |
Enrollment | 371 |
Est. completion date | December 18, 2018 |
Est. primary completion date | December 18, 2018 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 15 Years to 49 Years |
Eligibility |
Inclusion Criteria: - Women of reproductive age - Had an Safe Abortion (SA)/Post Abortion Care (PAC) procedure at one of six private clinics that day - Has her own cellphone that is WhatsApp compatible and will have access to this phone for the next four weeks - Willing to receive receive short message service (SMS) messages and phone calls from an Marie Stopes Kenya (MSK) or Innovation for Poverty Action (IPA) professional - Able to communicate in English and/or Swahili - Willing and able to comprehend and give informed consent - Willing to participate in a baseline survey immediately after providing consent - Willing to be followed up by phone at two weeks and four weeks post procedure for a 15-minute survey at each time-point - Has not already participated in this study Exclusion Criteria: - Is not a women of reproductive age - Did not have an SA/PAC procedure at one of six private clinics that day - Does not have her own cellphone that is WhatsApp compatible and will have access to this phone for the next four weeks - Is not willing to SMS messages and phone calls from an MSK/IPA professional - Is not able to communicate in English and/or Swahili - Is not willing or is not able to comprehend and give informed consent - Is not willing to participate in a baseline survey immediately after providing consent - Is not willing to be followed up by phone at two weeks and four weeks post procedure for a 15-minute survey at each time-point - Has already participated in this study |
Country | Name | City | State |
---|---|---|---|
Kenya | Marie Stopes International Kenya | Nairobi |
Lead Sponsor | Collaborator |
---|---|
University of California, San Francisco | Innovations for Poverty Action, Marie Stopes International |
Kenya,
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* Note: There are 25 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Person-Centered Abortion Scale Score | Survey conducted with women: self-report of experiences of PCC. Possible range 0-100; higher the score, better the experience | baseline | |
Primary | Person-Centered Abortion Scale Score | Survey conducted with women: self-report of experiences of PCC. Possible range 0-100; higher the score, better the experience | 2 weeks post-procedure | |
Primary | Person-Centered Abortion Scale Score | Survey conducted with women: self-report of experiences of PCC. Possible range 0-100; higher the score, better the experience | 4 weeks post-procedure | |
Secondary | Post abortion family planning counseling | Self-report if women received counseling on family planning (Yes/No) | baseline | |
Secondary | Post-abortion family planning uptake | Self-report of uptake of family planning (Yes/No/Refused to answer) | baseline | |
Secondary | Perceived social support | Medical Outcomes Study-Social Support 15-item Scale (MOS-SSS): 18-90 where higher scores indicate greater social support | baseline | |
Secondary | Perceived abortion stigma | The Individual Level Abortion Stigma Scale (ILAS Scale) Abbreviated 3-item Scale: 0-9 where higher scores indicate greater worry about stigma | baseline | |
Secondary | Mental Health | Mental Health Inventory (MHI-5) scale; 0-100 with higher scores indicating better mental health | baseline | |
Secondary | Post-abortion family planning uptake | self-report of uptake of family planning (Yes/No/Refused to answer) | 2 weeks post-procedure | |
Secondary | Mental Health | Mental Health Inventory (MHI-5) scale; 0-100 with higher scores indicating better mental health | 2-weeks post procedure | |
Secondary | Post-abortion family planning uptake | self-report of uptake of family planning (Yes/No/Refused to answer) | 4 weeks post-procedure | |
Secondary | Perceived social support | Medical Outcomes Study-Social Support 15-item Scale (MOS-SSS): 18-90 where higher scores indicate greater social support | 4 weeks post-procedure | |
Secondary | Perceived abortion stigma | The Individual Level Abortion Stigma Scale (ILAS Scale) Abbreviated 3-item Scale: 0-9 where higher scores indicate greater worry about stigma | 4 weeks post procedure |
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