To study the effectiveness of Udvartana in managing pain produced after Vyayama in Sthula.

CLINICAL EVALUATION OF EFFECTIVENESS OF UDVARTANA IN MANAGING PAIN INDUCED DUE TO VYAYAM IN STHULA(OVERWEIGHT/OBESE). - nil

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/02/080892

Enrollment

Registered

2025-02-19

Start date

Unknown

Completion date

Unknown

Last updated

2025-03-03

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

Conditions

Health Condition 1: E663- Overweight

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1. Subjects with BMI 23 to 39.9 kg m2, who don t practice exercise regularly. 2. Subjects who experience body pain after vyayama and with Defense and Veterans pain rating scale (DVPRS)equal to or greater than 03. 3. Subjects aged between 25 to 50 years irrespective of the gender occupation and socio-economic status. 4.Subjects who are fit for udvartana

Exclusion criteria

Exclusion criteria: 1. Subjects who are on regular analgesic medication. 2. Subjects with impaired mobility. 3. Subjects who are unfit for Vyayama. 4. Subjects who can t follow the instructions given

Design outcomes

Primary

Measure	Time frame
1. To study the effectiveness of udvartana in preventing pain given before vyayama on subjects with pain induced due to vyayama. 2. To study the effectiveness of udvartana in alleviating pain given after vyayama on subjects with pain induced due to vyayama. 3. To compare the effectiveness of udvartana given pre and post vyayama on subjects with pain induced due to vyayama in order to ascertain the best sequence. Timepoint: 5 DAYS	—

Measure

Time frame

1. To study the effectiveness of udvartana in preventing pain given before vyayama on subjects with pain induced due to vyayama. 2. To study the effectiveness of udvartana in alleviating pain given after vyayama on subjects with pain induced due to vyayama. 3. To compare the effectiveness of udvartana given pre and post vyayama on subjects with pain induced due to vyayama in order to ascertain the best sequence. Timepoint: 5 DAYS

—

Secondary

Measure	Time frame
1. BMI before and after the intervension. Timepoint: 5 DAYS	—

Countries

India

Contacts

Public ContactDr Adithi B

Sri Dharmasthala Manjunatheshwara College of Ayurveda and Hospital

drmbkavita@sdmcahhassan.org9447654298

Outcome results