Increasing recovery after abdominal surgery through education before surgery and care and follow up after surgery
Not Applicable
- Conditions
- Health Condition 1: null- Undergoing abdominal surgery
- Registration Number
- CTRI/2018/02/011919
- Lead Sponsor
- Self
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Age between 25-65 years
2.Patients undergoing elective laparotomy
Exclusion Criteria
1.Patients undergoing laparoscopic surgery
2.Patients with pre existing chronic airway disease/severe musculoskeletal problems
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method H1-There will be a significant difference in the parameters of postoperative recovery between the experimental group I ,II and the control groupTimepoint: Posttest will be conducted after 7 days
- Secondary Outcome Measures
Name Time Method H2-There will be a significant association between parameters of postoperative recovery and selected variablesTimepoint: 2 years