Effects of Tendon Neuroplastic Training on Pain, Range of Motion and Disability in Patients With Rotator Cuff Tendinopathy
Overview
- Phase
- Not Applicable
- Status
- Recruiting
- Enrollment
- 38
- Locations
- 1
- Primary Endpoint
- Numeric pain rate scale (NPRS)
Overview
Brief Summary
EFFECTS OF TENDON NEUROPLASTIC TRAINING ON PAIN, RANGE OF MOTION AND DISABILITY IN PATIENTS WITH ROTATOR CUFF TENDINOPATHY
Detailed Description
Rotator cuff tendinopathy is a condition where the shoulder's tendon suffers small tears or inflammation, often causing pain frequently arises from repetitive overuse or the natural aging process Regular overhead activities can aggravate the shoulder's wear and tear, leading to tendinosis. The purpose of this study is to evaluate and compare the impact of tendon neuroplastic training with standard treatments on pain levels, functional disability, and the range of motion in patients suffering from rotator cuff tendinopathy. Data were collected from Riphah rehabilitation clinic Lahore. Nprs , goinmeter and Spadi questioner were used before and after the intervention. Assessment was done through the tool before and after the treatment.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Single (Outcomes Assessor)
Masking Description
The study was single blinded, as accessor of the study were kept blind to the intervention groups
Eligibility Criteria
- Ages
- 18 Years to 65 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Have a current shoulder complaint lasting at least three months prior to the time of enrollment
- •Pain is located in the proximal lateral aspect of the upper arm (C5 dermatome)
- •Positive Hawkins-Kennedy test
Exclusion Criteria
- •Bilateral shoulder pain
- •Less than 90 degrees of active elevation of the arm
- •Corticosteroid injection within the last six weeks
- •Radiologically verified fracture
- •Glenohumeral osteoarthritis
- •Surgery or dislocation of the affected shoulder
- •Symptomatic arthritis in the Ac joint
- •Frozen shoulder
- •Symptoms derived from the cervical spine
Outcomes
Primary Outcomes
Numeric pain rate scale (NPRS)
Time Frame: 6 weeks
Patient level of pain will be assessed using this scale. This scale ranges from 0 to 10. 0 indicates "no pain" and 10 indicates "worst pain".
Shoulder pain and disability index (spadi)
Time Frame: 6 weeks
Patient level of disability will be assessed using this scale. This ranges from 0 to 100. 0 indicates no disability" and 100 indicates disability"
Universal Goniometer (UG)
Time Frame: 6 weeks
It will measure range of motion of shoulder
Secondary Outcomes
No secondary outcomes reported