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Assessment of Shoulder Rehabilitation Practices and Documentation Protocols at Riphah Rehabilitation Center

Completed
Conditions
Shoulder Pain
Rotator Cuff Injury
Shoulder Impingement
Registration Number
NCT06773442
Lead Sponsor
Riphah International University
Brief Summary

This study aims to evaluate Riphah Rehabilitation Center's shoulder rehabilitation procedures and documentation guidelines. The study will specifically assess the efficacy of shoulder rehabilitation procedures, their methodology, and the techniques employed to record patient improvement. In order to make sure the centre adheres to best practices, improves patient care, and keeps accurate records for better treatment outcomes, the study intends to identify areas of strength and potential improvements in both the rehabilitation techniques and documentation processes. The evaluation's findings will improve the center's operational effectiveness and clinical practices.

Target Audience:Healthcare Professionals (such as physicians, physiotherapists, and rehabilitation therapists): This study will assist guide evidence-based strategies for managing shoulder injuries and offer insights into contemporary rehabilitation procedures.

Centre Administration: For better patient care, resource management, and operational efficiency, the results will point out areas where documentation and treatment protocols should be strengthened.

Patients and Families: In the end, the study will improve rehabilitation results, increasing the likelihood that patients will heal from shoulder injuries more quickly and completely.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
20
Inclusion Criteria
  • Patients undergoing shoulder rehabilitation at Rphah Rehabilitation Center.
  • Rehabilitation protocols implemented within the center.
  • Documented cases with sufficient information for analysis.
  • Both acute and chronic shoulder conditions
Exclusion Criteria
  • Patients with shoulder conditions not requiring rehabilitation.
  • Cases lacking adequate documentation.
  • Rehabilitation protocols not specific to shoulder conditions.
  • Patients with comorbidities significantly affecting rehabilitation outcomes.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain Severity During Shoulder Rehabilitation TreatmentBaseline and 4 weeks (post-intervention)

Pain severity will be assessed using a Numerical Rating Scale (0-10), where 0 indicates no pain and 10 indicates the worst imaginable pain. Both groups will receive 2 treatment sessions per week. Pain assessments will be made at baseline (pre-intervention) and at the end of the 4-week intervention (post-intervention) to evaluate changes in pain severity.

Measurement Unit: Numerical Rating Scale (0-10), where 0 = no pain, 10 = worst possible pain.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Riphah Rehabilitation Center

🇵🇰

Lahore, Pakistan

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