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Evaluating the Effectiveness of a New CPR Training Program (PURE-LEAD) Among Diverse Community Groups in Mumbai.

Effectiveness of a PURE-LEAD Intervention on bystander CPR knowledge, attitude, self efficacy and procedural skill acquisition among specific vulnerable population cohorts across MMR: A multi-cohort interventional study - Uddharaksha PURE LEAD Bystander CPR Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/05/111128
Enrollment
804
Registered
2026-05-26
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: Uddharaksha PURE-LEAD Module: A copyrighted and content-validated training instrument based on the PURE-LEAD pedagogic construct (Performative, Unified, Rhythm-Entrained Lay-rescuer Edu

Sponsors

Dr Vaibhav Kumar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Verifiable membership of one of the six pre-specified cohorts (occupational identity card, gatekeeper-organization roster, or community-organization referral with self-declaration). Resident of, or working in, the Mumbai Metropolitan Region. Comprehension of Marathi, Hindi, or English. Provision of written informed consent. Functional capacity to perform chest compressions on a manikin (self-reported, with brief functional screen).

Exclusion criteria

Exclusion criteria: Healthcare professionals or individuals with formal certified cardiopulmonary resuscitation or basic life support training within the preceding 12 months Self reported musculoskeletal cardiac pulmonary or neurological condition that may prevent safe performance of chest compressions on a manikin Cognitive impairment or acute psychological distress that may interfere with valid assessment Inability to complete the baseline assessment Refusal to provide consent or withdrawal of consent at any stage

Design outcomes

Primary

MeasureTime frame
Change in overall CPR knowledge attitude self efficacy and skill scores measured using CARE CPR instrumentTimepoint: Baseline immediately post intervention 1 month 3 months—

Secondary

MeasureTime frame
Skill Fidelity Index (compression rate, depth, recoil, and hand placement).Timepoint: Immediate post-intervention and 1-month follow-up.;Domain-specific change scores (Individual Knowledge, Attitude, Self-efficacy, and Skill sub-scales)Timepoint: Baseline, Immediate Post-intervention, and 1-month follow-up;BCPR Hesitation Index and Resuscitation Self-Efficacy (RSE) scale.Timepoint: Baseline, Immediate Post-intervention, and 1-month follow-up;Implementation Outcomes (Acceptability/AIM, Appropriateness/IAM, Feasibility/FIM, and Cascade Multiplier Ratio).Timepoint: At the end of the intervention session.;Adverse Events (Musculoskeletal injury or psychological distress).Timepoint: Throughout the study duration.—

Countries

India

Contacts

Public ContactDr Vaibhav Kumar

Dr.G.D.Pol foundation, Y.M.T. Dental College and Hospital

drvaibhav1989@gmail.com9742501587

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026