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Using Technology-assisted exercise programs and Relaxation therapy to Reduce Pain and Improve Well-Being in Fibromyalgia

VIRTUAL REALITY-ASSISTED EXERCISE PROGRAM IN COMBINATION WITH GUIDED IMAGERY ON PATIENT-REPORTED SYMPTOMS IN FIBROMYALGIA - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/101433
Enrollment
30
Registered
2026-01-19
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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: VR Assisted exercises: Virtual reality (VR) technology immerses patients in a computer-generated environment that closely resembles the real world, enabling interactive experiences- 20

Sponsors

Kartika agarwal
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Widespread Pain Index more than or equal to 7 and Symptom Severity Score more than or equal to 5 2. Generalized pain present in more than or equal to 4 of 5 regions: left upper, right upper, left lower, right lower, axial 3. Symptoms present at a similar level for more than or equal to 3 months 4. Pain intensity: more than or equal to 5 on the Visual Analogue Scale at baseline 5. age of 25- 35 years 6. Physical activity status: Sedentary lifestyle- no structured exercise or irregular physical activity in the last 6 months

Exclusion criteria

Exclusion criteria: 1. Co-morbid autoimmune disorders 2. Serious medical illness, cognitive impairment, psychosis, suicidality, or recent alcohol/drug dependence 3. Surgery of the spine, vertebral fractures, sciatic pain, tumors 4. Previous myocardial infarction, lower extremity arterial disease, major neurological problems, diabetes, gastrointestinal disease, chronic respiratory disease, kidney disease

Design outcomes

Primary

MeasureTime frame
1.VAS 2.Pressure algometer 3. Penn Computerized Neurocognitive Battery 4.Hospital Anxiety and Depression Scale (HADS) Timepoint: 4 weeks, 3 times per week

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactKartika Agarwal

SGT University

Priyanka.sphy@sgtuniversity.org8588878467

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026