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NCT Number: NCT06707857

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

EFFECTS OF TENDON NEUROPLASTIC TRAINING ON PAIN, RANGE OF MOTION AND DISABILITY IN PATIENTS WITH ROTATOR CUFF TENDINOPATHY

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Riphah Rehabilitation clinic

Lahore, Punjab Province, Pakistan

Location status: Recruiting

Location contact

Ali Raza, MS-OMPT

CONTACT

0332 6099065

Sheeza kalsoom, MS-OMPT

SUB_INVESTIGATOR

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

tendon neuroplastic training

Other

Throughout the training, participants pain, range of motion and disability were monitored and they were asked to report any discomfort or unusual sign.

Conventional training

Other

Throughout the training, participants pain, range of motion and disability were monitored and they were asked to report any discomfort or unusual sign.

Primary outcomes

  1. 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".

  2. 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"

  3. Universal Goniometer (UG)

    Time frame: 6 weeks

    It will measure range of motion of shoulder

Study contacts

Contact information is provided by the study sponsor or research team.

Imran Amjad, Phd

CONTACT

[email protected]

03324390125

Sponsors and collaborators

Lead sponsor

Riphah International University

Other

Registry information

Official study title

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

Important dates

Study start
2024
Primary completion
2024
Study completion
2025
First posted
Nov 27, 2024
Registry last updated
Nov 27, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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