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Effect of exercise adherence app to find Improvement among orthopedic pain patients

Design, Development, and Effectiveness of SRIHER EXercise System which measures exercise adherence among musculoskeletal disorder individuals: A Randomized Controlled Crossover trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/10/075742
Enrollment
124
Registered
2024-10-23
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

Health Condition 1: M958- Other specified acquired deformities of musculoskeletal system

Interventions

Intervention1: SRIHER EXercise System: SRIHER EXercise System (Group A) receives STANDARD exercise as recommended by ACSM with APP study participant allocated in this group receives exercise and stan

Sponsors

Sri Ramachandra Institute of Higher Education and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Participants with Musculoskeletal (MSK) Pain 2. Participants referred for Physiotherapy with MSK Pain 3. Participants who gave consent to participate in the study

Exclusion criteria

Exclusion criteria: 1. Participants with diagnosis/ severe injury, in whom surgery is indicated. 2. Participants with a history of upper/ lower limb joint replacement/ surgery, spine surgery 3. Participants with corticoid injection within the past one month. 4. Participants with any congenital or acquired deformity in the spine or lower limb 5. Participants diagnosed with comorbidities - neurological conditions, psychiatric conditions, systemic diseases/cancer 6. Participants with unstable medical conditions 7. Participants not able to come for follow-ups / not willing to participate in the study 8. Participants with suspicion of chronic widespread pain 9. Participants with insufficient language comprehension.

Design outcomes

Primary

MeasureTime frame
Numerical rating scaleTimepoint: at Baseline, at the end of the 1st week, 2nd week, 4th week, 6th week, 8th week, 10th week, 12th week, 24th week.

Secondary

MeasureTime frame
Global perceived effectTimepoint: at Baseline, at the end of the 1st week, 2nd week, 4th week, 6th week, 8th week, 10th week, 12th week, 24th week.;Patient Reported Outcomes Measurement Information System (PROMIS)Timepoint: at Baseline, at the end of the 1st week, 2nd week, 4th week, 6th week, 8th week, 10th week, 12th week, 24th week.;Range of MotionTimepoint: at Baseline, at the end of the 1st week, 2nd week, 4th week, 6th week, 8th week, 10th week, 12th week, 24th week.;Muscle Strength/ enduranceTimepoint: at Baseline, at the end of the 1st week, 2nd week, 4th week, 6th week, 8th week, 10th week, 12th week, 24th week.;Quality of LifeTimepoint: at Baseline, at the end of the 1st week, 2nd week, 4th week, 6th week, 8th week, 10th week, 12th week, 24th week.

Countries

India

Contacts

Public ContactSoundararajan K

Sri Ramachandra Institute of Higher Education and Research

k.soundararajan1995@gmail.com09551163416

Outcome results

None listed

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