Population Services International
Lucknow, Uttar Pradesh, India
NCT Number: NCT04206527
To evaluate the impact of a training to ASHAs on person-centered care (PCC) for family planning (FP).
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Notify Me18 year–49 year
Female
Interventional
Not applicable
Lucknow, Uttar Pradesh, India
ASHAs will be provided with a training on family planning (FP) counseling and method options. Half of the group will receive additional trainings on person-centered care (PCC) principles and respectful care while the other half of the group will not receive this additional training. Women working with both the control ASHAs (FP trained) and Interventions ASHAs (FP+PCC trained) will be surveyed following their interactions with the ASHA to understand the quality of their experience with the ASHA and whether the woman has taken up a FP method of her choice following interaction with the ASHA.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
ASHAs provided with training on FP methods and counseling plus PCC for FP
Participation in an enhanced FP training including PCC
Time frame: 3-months after first FP counseling with ASHA
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: at least 3-months after FP training
In-depth interviews with ASHAs from intervention and control arms to understand experience providing FP counseling
Time frame: 3-months after first FP counseling with ASHA
Self-report of uptake of a FP method; Yes/No/I Don't remember
University of California, San Francisco
Other
Strengthening People-centered Accessibility, Respect, and Quality for Family Planning Services in India
Acronym: SPARQ_FPI
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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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