- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06773442
Assessment of Shoulder Rehabilitation Practices and Documentation Protocols at Riphah Rehabilitation Center
Assessment of Shoulder Rehabilitation Practices and Documentation Protocols at Rphah Rehabilitation Center, Lahore A Comprehensive Analysis
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.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Lahore, Pakistan, 54840
- Riphah Rehabilitation Center
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Punjab
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Lahore, Punjab, Pakistan
- Riphah Rehabilitation Center
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Patients Undergoing Shoulder Rehabilitation:
Include patients who have undergone or are currently undergoing rehabilitation specifically for shoulder injuries, conditions, or surgeries.
Consider both inpatients and outpatients receiving rehabilitation services at Rphah Rehabilitation Center.
Description
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 Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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GROUP A:Rehabilitation Practices Group:
Objective: Evaluate the effectiveness and quality of shoulder rehabilitation practices. Data Collection, Observation of rehabilitation sessions: Record types of exercises, therapy techniques, patient engagement, and therapist-patient interactions. Interviews with rehabilitation professionals: Gather insights into their approaches, challenges faced, and perceived effectiveness of rehabilitation strategies. Analysis: Assess adherence to established rehabilitation protocols. Evaluate patient outcomes such as pain levels, range of motion, and functional status. Compare observed practices with evidence-based guidelines for shoulder rehabilitation. Findings: Identify strengths and weaknesses in current rehabilitation practices. Highlight areas where improvements or modifications may be necessary. |
Evidence-Based Training Program:Develop a structured training program for rehabilitation professionals focusing on evidence-based shoulder rehabilitation practices. Clinical Mentorship and Supervision:Implement a mentorship program where experienced rehabilitation professionals provide guidance and support to junior staff members. Standardization of Rehabilitation Protocols:Review and standardize rehabilitation protocols for common shoulder conditions based on current evidence and best practices. Patient-Centered Care Approach:Adopt a patient-centered approach to shoulder rehabilitation, emphasizing shared decision-making and individualized treatment plans Outcome Monitoring and Quality Improvement:Use standardized outcome measures to evaluate improvements in pain, function, range of motion, and patient satisfaction. |
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GROUP B:Documentation Protocols Group
Objective: Assess the completeness, accuracy, and organization of documentation related to shoulder rehabilitation. Data Collection: Review of patient records and documentation: Evaluate the quality and consistency of documentation practices, including initial evaluations, progress notes, and discharge summaries. Interviews with rehabilitation staff: Collect feedback on documentation protocols, challenges encountered, and perceived adequacy of documentation practices. Analysis: Assess the clarity and comprehensiveness of documentation. Evaluate adherence to documentation protocols and standards. Identify any deficiencies or inconsistencies in documentation practices. Findings: Highlight strengths and weaknesses in current documentation protocols. Identify areas for improvement, such as standardizing documentation templates or providing training on effective documentation practices. Recommendations: Propose strategies to enhance documentation quality and consistency. |
Training and Education Program:Develop and implement a training program for rehabilitation professionals aimed at enhancing their knowledge and skills in shoulder rehabilitation practices and documentation protocols. Standardization of Protocols:Review and update existing rehabilitation protocols to ensure alignment with current evidence-based guidelines and best practices. Quality Assurance Measures:Establish a system for ongoing monitoring and evaluation of shoulder rehabilitation practices and documentation protocols. Patient Education and Engagement:Develop educational materials and resources for patients undergoing shoulder rehabilitation to enhance their understanding of treatment goals, exercises, and self-management strategies. Outcome Monitoring and Evaluation:Implement a system for monitoring and evaluating patient outcomes, including pain levels, range of motion, functional status, and satisfaction with rehabilitation services. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Pain Severity During Shoulder Rehabilitation Treatment
Time Frame: Baseline and 4 weeks (post-intervention)
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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. |
Baseline and 4 weeks (post-intervention)
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Muhammad Hashim, Riphah International University
Publications and helpful links
General Publications
- Smith BA, Fields CJ, Fernandez N. Physical therapists make accurate and appropriate discharge recommendations for patients who are acutely ill. Phys Ther. 2010 May;90(5):693-703. doi: 10.2522/ptj.20090164. Epub 2010 Mar 18.
- Scalzitti DA. On
- De Villers MJ. Documentation of preventive education and screening for osteoporosis. Outcomes Manag. 2003 Jan-Mar;7(1):28-32.
- Ajami S, Arab-Chadegani R. Barriers to implement Electronic Health Records (EHRs). Mater Sociomed. 2013;25(3):213-5. doi: 10.5455/msm.2013.25.213-215.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/RCR&AHS24/37
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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