MedPath

To study whether brief interventions are effective in reducing fear of childbirth and impact self-efficacy among first time mothers

Phase 1
Registration Number
CTRI/2019/11/021950
Lead Sponsor
Mr Dan Isaac Pothiyil
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Primigravid singleton delivery

2. Must be able to read and speak Kannada and/or English

3. Women who voluntarily consent to participate

Exclusion Criteria

1. Women with planned cesarean delivery

2. Women anticipating or experiencing a perinatal death (congenital abnormality incompatible) or stillbirth

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1. Fear of Childbirth <br/ ><br>2. Self-EfficacyTimepoint: 1. Baseline on first contact <br/ ><br>2. Post intervention (1-2 days) <br/ ><br>3. Post delivery (1 day)
Secondary Outcome Measures
NameTimeMethod
a. Expectations from Childbirth <br/ ><br>b. Experience of ChildbirthTimepoint: For a. <br/ ><br>1. Baseline on first contact <br/ ><br>2. Post intervention (1-2 days) <br/ ><br>For b. <br/ ><br>1. Post delivery (1 day)
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