Jacobson’s Technique on Postoperative Pain, Activity Tolerance and Sleeping
Not Applicable
Recruiting
- Conditions
- Patients Undergoing Gynaecological Surgery.
- Registration Number
- IRCT20210131050193N1
- Lead Sponsor
- Damanhour University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 116
Inclusion Criteria
patients undergoing abdominal gynaecological surgery for benign conditions, being able to differentiate between the different images in visual analogue scale, being free from any psychological or mental disorders, taking non-steroidal anti-inflammatory medication as post-operative analgesia, and being enthusiastic about contributing in the study.
Exclusion Criteria
Drug abusers, alcoholics, those who undergo laparoscopic surgery, drink more than 3 cups of coffee per day, use sleep medications, and had intra or post-operative complications will be excluded from the study.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative Pain, Activity Tolerance and Sleeping Quality. Timepoint: before intervention and 2, days after intervention. Method of measurement: pain analogue scale; activity tolerance questionnaire, and the Groningen sleeping quality scale.
- Secondary Outcome Measures
Name Time Method one. Timepoint: None. Method of measurement: None.