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A prospective single center study to assess the effect of pre operative spiritual intervention on stress in patients post surgery

Not Applicable
Conditions
Health Condition 1: F09- Unspecified mental disorder due toknown physiological condition
Registration Number
CTRI/2021/12/038576
Lead Sponsor
il
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Closed to Recruitment of Participants
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patients of the gynecological department undergoing major surgery at Bhaktivedanta

Hospital.

Patients of under the age group of 18-65

Exclusion Criteria

Patients in the ICU

Patients without signed ICF

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To assess the effect of spiritual intervention on stress levels, acute and chronic pain levels and negative emotional symptomsTimepoint: Assessment of the patient would be performed pre operation (before the surgery) and post operation (after 24 hours of the surgery). <br/ ><br>Mode of assessment is verbal (questionnaire).
Secondary Outcome Measures
NameTimeMethod
Vital signs such as blood pressure, pulse rate, and oxygen saturation. <br/ ><br>Overall wellbeing of the patientsTimepoint: Every 4 hours
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