A study to assess use of abdominal binder after cesarean section on maternal comfort and functional outcome
Not Applicable
Not yet recruiting
- Conditions
- Health Condition 1: O754- Other complications of obstetric surgery and proceduresHealth Condition 2: O754- Other complications of obstetric surgery and procedures
- Registration Number
- CTRI/2022/05/042690
- Lead Sponsor
- PGIMER
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Post Cesarean Section women with spinal anaesthesia
2.Those who are willing participate in the study
Exclusion Criteria
•Women with cardiopulmonary, neuromuscular and mental disorders
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcomes will be numeric pain rating scale-assessing pain, symptom distress scale (SDS)-assessing distressTimepoint: primary outcome will be post ceasarean pain and distress and will be assessed at post ceasarean 8hr, 24 hr, 48hr, at the time of discharge and 1st follow-up
- Secondary Outcome Measures
Name Time Method Secondary outcome will be functional outcome including mobolization assessed by 6minute walk test, self care activities assessed by barthal index scale and maternal satisfaction scale <br/ ><br>Timepoint: Secondary outcome will be assessed at post ceasarean 8hr, 24 hr, 48hr, at the time of discharge and 1st follow-up