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Keeping Mothers Safe: Finding the Causes and Prevention of Heavy Bleeding After Delivery

Assessment of risk factors and efficacy of multifaceted intervention to prevent primary Post Partum Hemorrhage among Pregnant women. - nil

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/10/096734
Enrollment
300
Registered
2025-10-31
Start date
Unknown
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Health Condition 1: O269- Pregnancy related conditions, unspecified

Interventions

Intervention1: mutifaceted intervention (structured teaching program): Introduction to PPH Causes and Risks Recognizing PPH Danger Signs Birth Preparedness and Complication Readiness (BPCR) Nutrition

Sponsors

PRINCIPAL NVESTIGATOR
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Pregnant women between 16 to 28 weeks of gestation Pregnant women may be primigravida or multigravida Low to moderate PPH risk Age multiparty mild anemia Malnutrition mild Gestational Hypertension Willing to participate and available for data collection. Women who provide informed consent to participate in the study or intervention

Exclusion criteria

Exclusion criteria: High-Risk Cases: Women identified as high-risk for PPH those with a history of PPH placenta previa or placental abruption Previous Caesarean section deliver Women who do not provide informed consent Women who are not willing to participate.

Design outcomes

Primary

MeasureTime frame
The primary outcome of the study is the improvement in knowledge and preparedness regarding the prevention and early recognition of primary postpartum hemorrhage among antenatal mothers. This will be measured using a structured knowledge questionnaire administer afterthe educational intervention.Timepoint: At 16-28 weeks of gestation One day 10 samples are selected and then to be continued for the rest days till 200 samples 10 samples each day 20 days for 200 sample selection On same day educational intervention Then administer structured knowledge questionnaire on same day At 32-38 weeksgroup discussion with completion of Participant Feedback form to evaluate efficacy of intervention around 20 mothers each day so 10 days for 200 mother.—

Secondary

MeasureTime frame
reduce MMR in pph mother prevalence after interventionTimepoint: 06 month—

Countries

India

Contacts

Public ContactSEEMA SARKAR

Teerthanker Mahaveer University, Moradabad, Uttar Pradesh

seema.scholar@tmu.ac.in8116345398

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Aug 10, 2026