A research to study the efficacy of pain reprocessing therapy, an intervention for pain for patients of Fibromyalgia in comparison with the Jacobsons Progressive Muscle Relaxation.
Phase 1
Not yet recruiting
- Conditions
- Health Condition 1: M797- Fibromyalgia
- Registration Number
- CTRI/2023/11/059606
- Lead Sponsor
- Amrita Institute Of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Males and females of age ranging from 20 to 55 years.
Individuals who are diagnosed with Fibromyalgia.
Individuals with minimum 10 years of education
Exclusion Criteria
No reported history of traumatic brain injury.
No reported physical disorders where pain is primary complaint.
No reported history of chronic neurological condition where pain is the primary symptom.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method A comparison of Pre- intervention and post-intervention scores on Bodily and Emotional Perception of Pain questionnaire (BEEP) in both groups will be considered as primary outcome. <br/ ><br>Timepoint: Time points: <br/ ><br>Pre intervention <br/ ><br> <br/ ><br>Baseline assessments <br/ ><br> <br/ ><br>Post intervention: <br/ ><br>5 weeks <br/ ><br> <br/ ><br>Follow up assessmnent: <br/ ><br>9 weeks
- Secondary Outcome Measures
Name Time Method To assess the Bodily and Emotional Perception of Pain <br/ ><br>To assess the symptoms severity before and after PRT by using behavioural evaluation measures. <br/ ><br>To assess the effect of PRT at one month follow up. <br/ ><br>Timepoint: 1 month post intervention