Study of effect of Garbhsamskar programme on the quality of life of a pregnant wome
Not Applicable
- Conditions
- Health Condition 1: O80- Encounter for full-term uncomplicated delivery
- Registration Number
- CTRI/2023/06/054050
- Lead Sponsor
- Bhaktivedanta Hospital Research Institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Closed to Recruitment of Participants
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patients who have completed four sessions of Garbhasamskar would be enrolled in interventional group.
2.Pregnant women who didn’t attended Garbhasamskar would go in control arm.
3.Participants who would voluntarily consent can participate.
4.Participants of any age who has conceived.
Exclusion Criteria
1.Participants not willing to consent for the study
2.Mentally retarded participants .
3.Participants who may not comply to the study procedures as per the Investigator’s discretion .
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To check the effect of quality of life of pregnant women with respect to Physical , Mental , Social and Spiritual welbeing aspectsTimepoint: 1 Week <br/ ><br>35 Week
- Secondary Outcome Measures
Name Time Method To check the effect of Garbhsamskar program on pregnancy related complications such as Pregnancy Induced Hypertension (PIH), Diabetes Mellitus ( DM),Post partum haemorrhage ( PPH) and Intrauterine growth retardation ( IUGR)Timepoint: 37 Week