Actively Recruiting

Phase Not Applicable
Age: 40Years - 60Years
All Genders
ID07203963

Additional Effects of Niel Asher Technique Along With Sleeper Stretch on Posterior Capsule in Patients With Adhesive Capsulitis

Led by Riphah International University · Updated on 2025-11-24

36

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to evaluate the additional effects of the Niel-Asher technique combined with sleeper stretch and conventional physical therapy on reducing pain, improving shoulder ranges of motion, and enhancing functional ability in patients with Adhesive Capsulitis, also known as frozen shoulder. Adhesive capsulitis is a painful condition marked by stiffness and reduced movement in the shoulder joint, often caused by fibrosis and contracture of the joint capsule. It is more common in females aged 40 to 60 and leads to significant limitations in shoulder rotation and other movements. The study compares two treatment approaches: one group receives the Niel-Asher technique along with sleeper stretch and conventional therapy, while the other group receives only sleeper stretch and conventional therapy. The Niel-Asher technique involves deep stroking massage and compression of trigger points on major shoulder muscles, applied three times a week for four weeks. Sleeper stretch is applied passively by the investigator to improve shoulder flexibility, also three times a week. Conventional therapy includes joint glides, active and assisted range of motion exercises, isometric exercises, Codman's and pulley exercises, and ischemic pressure to release trigger points. Participants will be involved in treatment sessions over four weeks, with assessments at the end of this period. Researchers will measure pain levels using the Visual Analogue Scale (VAS), shoulder function and disability with the Shoulder Pain and Disability Index (SPADI), and shoulder range of motion using a goniometer. These measures will help evaluate how the treatments affect pain, movement, and daily function. The trial is randomized and single-blinded, with follow-up planned to monitor progress and treatment effects up to four weeks.

CONDITIONS

Brief Title

Additional Effects of Niel-asher Technique on Patients With Adhesive Capsulitis

Who Can Participate

Age: 40Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 40 and 60 years
  • Male or female gender
  • Diagnosed with adhesive capsulitis by an orthopedic or general physician
  • Painful and limited active and passive shoulder movement following the capsular pattern (external rotation > abduction > internal rotation)
  • In phase two or three of adhesive capsulitis based on symptom duration
  • Presence of trigger points in at least one or two of the rotator cuff or deltoid muscles according to Simon and Travell's criteria
Not Eligible

You will not qualify if you...

  • Spinal injuries or other co-morbid conditions
  • History of surgery, infection, trauma, pregnancy, fracture, or recent fall
  • Intra-articular steroid therapy within the last 6 months
  • Unwillingness to comply with follow-up schedule
  • Participation in another intervention study
  • Malignancy
  • Thyroid disorders, rheumatoid arthritis, or glenohumeral osteoarthritis
  • Previous surgery or manipulation under anesthesia of the affected shoulder
  • Duration of symptoms less than three months

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 - 4 weeks

Participants receive either the Niel-Asher Technique combined with sleeper stretch and conventional physical therapy or sleeper stretch with conventional physical therapy to reduce pain and improve shoulder function.

3 visits per week for 4 weeks

Trial Site Locations

Total: 1 location

1

Shafi International Hospital

Islamabad, Punjab Province, Pakistan, 46600

Actively Recruiting

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Research Team

K

KINZA ANWAR, MS-OMPT

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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