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A clinical trial to study the effect of audio-visual therapy on labor pain and anxiety in laboring women.

Not Applicable
Completed
Registration Number
CTRI/2021/09/036285
Lead Sponsor
I
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
84
Inclusion Criteria

Primigravida woman

- Admitted to the delivery room.

- Term singleton pregnancy (� 37 weeks)

- Being in the active phase of labor (cervical dilatation 4-8 cm)

- Having no obstetric risks.

- Not receiving any analgesia.

- Gives consent to participate in the study.

Exclusion Criteria

- Woman in labor who is either blind or deaf or both.

- Women who could not complete 2 hours of intervention prior to beginning of second stage of labor.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
abor pain perception and maternal anxiety <br/ ><br>Timepoint: Pre intervention <br/ ><br>After 20, 40, 60, 80 minutes
Secondary Outcome Measures
NameTimeMethod
Analgesic seeking frequency <br/ ><br>Timepoint: Throughout labor;Maternal outcomes <br/ ><br>Timepoint: Pre intervention <br/ ><br>After 20, 40, 60, 80 minutes <br/ ><br>After birth;Maternal satisfactionTimepoint: 1 hour after delivery;Neonatal outcomesTimepoint: After birth
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