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TO FIND OUT THE EFFECT OF VARIOUS ALTERNATIVE TREATMENTS IN WOMEN WITH MUSCULOSKELETAL PAIN AND STIFFNESS AND TENDERNESS AT SPECIFIC BODY SITES.

Role of alternative therapies in Fibromyalgia in women- A Clinical Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/04/041601
Enrollment
109
Registered
2022-04-04
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: M797- Fibromyalgia

Interventions

Intervention1: MANUAL THERAPY AND THERAPEUTIC EXERCISES FOR 10 WEEKS: MANUAL THERAPY AND THERAPEUTIC EXERCISES IN GROUP-A FOR 10 WEEKS Intervention2: MANUAL THERAPY AND COGNITIVE BEHAVIOUR THERAPY FOR

Sponsors

DrPriyanka Sethi
Lead Sponsor

Eligibility

Inclusion criteria

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

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.

Design outcomes

Primary

MeasureTime frame
1. Pain Intensity 2. Tenderness 2. Quality of Life Timepoint: 1. Baseline(Pre-Intervention) 2. Post Intervention-I(After 4 weeks from the baseline study) 3. Post Intervention-II (After 6 weeks from the Post Intervention-I Readings) 4 Follow up (After 2 weeks from Post Intervention-II Readings)

Secondary

MeasureTime frame
Activities of Daily LivingTimepoint: 1. Baseline(Pre-Intervention) 2. Post Intervention-I(After 4 weeks from the baseline study) 3. Post Intervention-II (After 6 weeks from the Post Intervention-I Readings) 4 Follow up (After 2 weeks from Post Intervention-II Readings)

Countries

India

Contacts

Public ContactPriyanka Sethi

Delhi Pharmaceutical Sciences and Research University

vkc.chorsiya@gmail.com8010003463

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026