TO FIND OUT THE EFFECT OF VARIOUS ALTERNATIVE TREATMENTS IN WOMEN WITH MUSCULOSKELETAL PAIN AND STIFFNESS AND TENDERNESS AT SPECIFIC BODY SITES.
Not Applicable
- Conditions
- Health Condition 1: M797- Fibromyalgia
- Registration Number
- CTRI/2022/04/041601
- Lead Sponsor
- DrPriyanka Sethi
- 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.Subjects meeting the criteria of -
2.Subjects with chronic pain � 6 months.
3.Married and living with partner
4.Local tenderness at 12 of 14 specified sites.
5. Disturbed sleep, with morning fatigue and stiffness.
6. Subjects those are willing to discontinue taking all pain relieving medications(analgesics and NSAIDS, except paracetamol upto 4g/day.
7. Normal laboratory findings
Exclusion Criteria
1.Participant Refusal
2.pregnant women
3. patients with history of a chronic medical conditions like: malignancy, systemic inflammatory disorders.
4.Subjects under treatment of psychiatric conditions and neurological disorders
5. Patients with any history of recent surgery.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Pain Intensity <br/ ><br>2. Tenderness <br/ ><br>2. Quality of Life <br/ ><br>Timepoint: 1. Baseline(Pre-Intervention) <br/ ><br>2. Post Intervention-I(After 4 weeks from the baseline study) <br/ ><br>3. Post Intervention-II (After 6 weeks from the Post Intervention-I Readings) <br/ ><br>4 Follow up (After 2 weeks from Post Intervention-II Readings)
- Secondary Outcome Measures
Name Time Method Activities of Daily LivingTimepoint: 1. Baseline(Pre-Intervention) <br/ ><br>2. Post Intervention-I(After 4 weeks from the baseline study) <br/ ><br>3. Post Intervention-II (After 6 weeks from the Post Intervention-I Readings) <br/ ><br>4 Follow up (After 2 weeks from Post Intervention-II Readings)