Mobile application for Shoulder rehabilitation
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 30
- Locations
- 1
- Primary Endpoint
- Enhanced functional recovery, including improvements in shoulder function, range of motion,strength, and mobility, as measured by validated
Study Overview
Brief Summary
The mobile application for shoulder rehabilitation aims to enhance the recovery process and outcomes for patients . Through a user-friendly platform, the app guides patients through their rehabilitation exercises, tracks their progress, and educates them about recovery journey. Furthermore, it fosters communication between patients and healthcare providers, facilitating timely support and guidance. Overall, the app seeks to improve patient engagement and adherence to rehabilitation protocols, ultimately leading to better recovery outcomes and overall satisfaction with the treatment process
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Masking
- Participant and Investigator Blinded
Eligibility Criteria
- Ages
- 18.00 Year(s) to 60.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Patients who needs shoulder rehabilitation Individuals who have access to a smartphone or tablet device with internet connectivity.
- •Participants willing and able to engage in post-operative rehabilitation exercises and activities.
- •Patients with sufficient understanding and proficiency in the language(s) supported by the mobile application.
- •Patients who have completed the immediate post-operative recovery phase and have been cleared by their healthcare provider to begin rehabilitation.
Exclusion Criteria
- •Individuals with cognitive impairments or mental health conditions that may affect their ability to use the mobile application effectively.
- •Patients with contraindications or complications that require specialized rehabilitation interventions beyond the scope of the mobile application.
- •Participants with severe mobility limitations or comorbidities that may prevent them from safely performing rehabilitation exercises.
- •Patients who are unable or unwilling to provide informed consent for participation in the study.
- •Individuals currently participating in other rehabilitation programs or clinical trials , to avoid confounding variables.
Outcomes
Primary Outcomes
Enhanced functional recovery, including improvements in shoulder function, range of motion,strength, and mobility, as measured by validated
Time Frame: 3 weeks after the start of rehabilitation
clinical scales over the study period.
Time Frame: 3 weeks after the start of rehabilitation
Secondary Outcomes
- Improved rehabilitation adherence rates assessed through engagement metrics in the mobile application.(Increased patient satisfaction evaluated via standardized satisfaction surveys.)
Investigators
Naveen Kumar
Saveetha medical college and hospital