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Effect of Shoulder Exercise Program on Pain and Confidence in Competitive Swimmers with Shoulder pain

THE EFFICACY OF RESILIENT SHOULDER REHABILITATION ON PAIN AND FEAR AVOIDANCE BEHAVIOR AMONG COMPETITIVE SWIMMERS WITH ROTATOR CUFF RELATED SHOULDER PAIN - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/109465
Enrollment
40
Registered
2026-04-27
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

None listed

Interventions

Intervention1: Resilient Shoulder Rehabilitation Program: The Resilient Rehabilitation for Rotator Cuff Related Shoulder Pain program is a structured progressive shoulder rehabilitation protocol desig

Sponsors

Shradha
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Subjects voluntarily willing to participate and who have signed a written informed consent form Subjects willing to comply with the rehabilitation protocol Competitive swimmers aged 19 years to 35 years who are actively participating Swimmers training for 6 to 8 hours per week or completing 4 to 5 training sessions per week Swimmers with unilateral shoulder pain Subjects with shoulder pain for more than 3 months Presence of any three positive signs Neers impingement test Hawkins Kennedy test painful arc drop arm test or pain on resisted external rotation State and district level competitive swimmers Swimmers with more than 3 years of experience Score of 4 or more on SFPS Score of more than 20 on AFAQ

Exclusion criteria

Exclusion criteria: Subjects with history of shoulder trauma Subjects with history of recurrent shoulder dislocation Subjects with any history of shoulder surgery within the past year Subjects who have received steroid or PRP injection in the shoulder within the last 3 months

Design outcomes

Primary

MeasureTime frame
Swimmers Functional Pain Scale Athlete Fear Avoidance QuestionnaireTimepoint: At the baseline and 6 weeks At the baseline and 6 weeks

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDr Pruthviraj R

RV College of Physiotherapy

principal.rvcp@rvei.edu.in9886590506

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026