Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
ID06707857

Effects of Tendon Neuroplastic Training on Pain, Range of Motion and Disability in Patients With Rotator Cuff Tendinopathy

Led by Riphah International University · Updated on 2024-11-27

38

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Rotator cuff tendinopathy is a condition where the shoulder's tendon suffers small tears or inflammation, often caused by repetitive use or aging. This condition can lead to pain, reduced range of motion, and disability. The study evaluates and compares the effects of tendon neuroplastic training with conventional therapy on pain, shoulder movement, and functional disability in patients with rotator cuff tendinopathy. Data were collected from a rehabilitation clinic using pain scales, range of motion measurements, and disability questionnaires. Participants are randomly assigned to one of two groups. Group A receives tendon neuroplastic training, performing slow, progressive exercises paced to an external audio cue on a smartphone three times a week for six weeks. This includes isolated abduction, external rotation, internal rotation, and flexion movements. Group B undergoes conventional therapy involving isometric contractions at 90 degrees of arm elevation, with resistance set based on maximal voluntary isometric strength. Both groups have their pain, range of motion, and disability monitored throughout the training. During the study, participants complete assessments before and after the six-week intervention using tools such as the Numeric Pain Rate Scale, Shoulder Pain and Disability Index, and Universal Goniometer. Researchers monitor pain levels, shoulder movement, and functional disability, recording any discomfort or unusual signs. The study aims to understand how these therapies may affect shoulder function and pain over the treatment period.

CONDITIONS

Brief Title

Effects of TNT on Pain, ROM and Disability in Patients With RC Tendinopathy

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Have a current shoulder complaint lasting at least three months prior to enrollment
  • Pain located in the proximal lateral aspect of the upper arm (C5 dermatome)
  • Positive Hawkins-Kennedy test
  • Aged between 18 and 65 years
  • Both genders eligible
Not Eligible

You will not qualify if you...

  • 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 Acromioclavicular joint
  • Frozen shoulder
  • Symptoms derived from the cervical spine

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 6 weeks

Participants undergo either tendon neuroplastic training or conventional training exercises focused on shoulder muscles to improve pain, range of motion, and disability.

3 supervised exercise sessions per week

Follow-up

Duration - Assessment at 6 weeks after treatment start

Participants are assessed for changes in pain, range of motion, and disability after completing the treatment.

1 visit (in-person)

Trial Site Locations

Total: 1 location

1

Riphah Rehabilitation clinic

Lahore, Punjab Province, Pakistan

Actively Recruiting

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Research Team

I

Imran Amjad, Phd

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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