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Yoga for general weakness and pain

Comparative efficacy of Yogic Suksma Vyayama in reducing general body stiffness and fatigue, improving flexibility and quality of life in heavy workers : A parallel randomized control trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/04/042083
Enrollment
128
Registered
2022-04-22
Start date
Unknown
Completion date
Unknown
Last updated
2022-05-02

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

Conditions

Health Condition 1: R299- Unspecified symptoms and signs involving the nervous and musculoskeletal systems

Interventions

Intervention1: Suksama vyayama: yogic sukshma vyayamasall the head to toe joints movement exercises for a duration of one month, 5 days a week i.e. from Monday to Friday,45 minutes. Control Intervent

Sponsors

Sant Hirdaram Medical College Of Naturopathy And Yogic ScienceS For Women
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients aged between 25 to 50 years old. Both male and female participants. Patients not undergoing any treatment with analgesics. Patients with Chalder fatigue scale (C.F.S. score) more than 15.

Exclusion criteria

Exclusion criteria: Patients below 25 and above 50 years old. Pregnant and lactating women. Regular practitioners of yoga for last 6 months Patients with Chalder fatigue scale (C.F.S. score) less than 15.

Design outcomes

Primary

MeasureTime frame
Chalderâ??s fatigue scale (C.F.S.)Timepoint: Before starting the study and after completion of one month intervention and after follow up period of one month.—

Secondary

MeasureTime frame
Burnout questionnaire. Timepoint: Before starting the study and after completion of one month intervention and after follow up period of one month.;Pain visual analog scale.Timepoint: Before starting the study and after completion of one month intervention and after follow up period of one month.;Hand Dynamometer. Timepoint: Before starting the study and after completion of one month intervention and after follow up period of one month.;SF-8 Quality of life questionnaire developed by RAND Corporation. Timepoint: Before starting the study and after completion of one month intervention and after follow up period of one month.;Sit and Reach Test. Timepoint: Before starting the study and after completion of one month intervention and then after follow up period of one month.—

Countries

India

Contacts

Public ContactDr Pardeep Nair

Sant Hirdaram Medical College Of Naturopathy And Yogic Sciences For Women

Fogawatkavita555@gmail.com9549025480

Outcome results

None listed

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