Quality Improvement Project for Reproductive Health Services in India, Phase 1 (SPARQ_QII1)

University of California San Francisco (UCSF)

Status: Completed

Conditions: Delivery; Reproductive Health; Maternal Health

Treatments: Behavioral: QI Collaborative

Study type: Interventional

Funder types: Other

Identifiers

NCT04208867

15-18008_IndiaQI1

Details and patient eligibility

About

Evaluation of a quality improvement (QI) collaborative aimed at improving person-centered care (PCC) for reproductive health (RH) services.

Full description

Evaluation of a quality improvement (QI) collaborative in public facilities in Uttar Pradesh, India aimed at improving person-centered care (PCC) for reproductive health (RH) services.

Enrollment: 2,989 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria for Women:

• Women aged 18-49
• Agree/consent to participate
• Delivered a baby at the facility within 7 days (or adopted a family planning method at time of visit (baseline only, not part of intervention))

Exclusion Criteria for Women:

• Not a women aged 18-49
• Did not agree/consent to participate
• Did not deliver a baby at the facility within 7 days (or adopted a family planning method at time of visit (baseline only, not part of intervention))

Inclusion Criteria for Providers:

• Agreed/consented to participate
• Staff at facility

Exclusion Criteria for Provider:

• Did not agree/consent to participate
• Not Staff at facility

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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2,989 participants in 4 patient groups

Intervention - Women

Experimental group

Description:

Women who receive MH services from a facility participating in the QI collaborative to improve PCC

Treatment:

Behavioral: QI Collaborative

Control - Women

No Intervention group

Description:

Women who receive MH services from a facility not participating in the QI collaborative to improve PCC

Intervention - Provider

Experimental group

Description:

Provider working at a facility participating in the QI collaborative to improve PCC

Treatment:

Behavioral: QI Collaborative

Control - Provider

No Intervention group

Description:

Provider working at a facility not participating in the QI collaborative to improve PCC