Reproductive Health
Conditions
Keywords
post abortion, person-centered care
Brief summary
The purpose of this study is to understand the effect of a phone based post-abortion intervention on the experience of post-abortion care.
Detailed description
This study evaluates whether personalized text messages and phone calls to post abortion women can improve post abortion person-centered care, perceived social support, post-abortion family planning, and reduce perceptions of social stigma and stress. Women were randomized to one of three study arms: personalized communication with a peer counselor or nurse who received person-centered care (PCC) training, or a control arm where participants received the standard of care.
Interventions
Post abortion phone based support
Sponsors
Study design
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
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Person-Centered Abortion Scale Score | baseline | Survey conducted with women: self-report of experiences of PCC. Possible range 0-100; higher the score, better the experience |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Mental Health | baseline | Mental Health Inventory (MHI-5) scale; 0-100 with higher scores indicating better mental health |
| Perceived abortion stigma | baseline | The Individual Level Abortion Stigma Scale (ILAS Scale) Abbreviated 3-item Scale: 0-9 where higher scores indicate greater worry about stigma |
| Post abortion family planning counseling | baseline | Self-report if women received counseling on family planning (Yes/No) |
| Post-abortion family planning uptake | baseline | Self-report of uptake of family planning (Yes/No/Refused to answer) |
| Perceived social support | baseline | Medical Outcomes Study-Social Support 15-item Scale (MOS-SSS): 18-90 where higher scores indicate greater social support |
Countries
Kenya