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Completed

NCT Number: NCT04057170

Manual Therapy Versus Conventional Rehabilitation Protocol on Subacromial Pain Syndrome

This study compares the periodic effects of Accelerated rehabilitation protocol (ARP) and Mulligan mobilization with mowement method (MWM) in subacromial pain syndrome patients rehabilitation. Half of the participants will receive ARP, while the other half will receive MWM.

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Key information

Conditions

Subacromial Impingement Syndrome Arthralgia Joint Diseases Musculoskeletal Diseases Neurologic Manifestations Pain Pathological Conditions, Signs and Symptoms Shoulder Impingement Syndrome Shoulder Injuries Shoulder Pain Signs and Symptoms Wounds and Injuries

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Volkan Deniz

Ankara, 06560, Turkey (Türkiye)

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • to be in the 18-60 age range, to be cooperative during evaluation and treatment and to accept to participate in the study

Exclusion criteria

  • the presence of adhesive capsulitis, surgical indication or shoulder surgery, cervicothoracic problems (such as stenosis and disc herniation) diagnosed as neurological or inflammatory joint diseases

Treatment and study plan

accelerated protocol and mulligan method

Other

manual therapy technic

Primary outcomes

  1. Shoulder Pain and Disability Index

    Time frame: two weeks

    It consists of 13 questions in two sections as 5 pain questions and 8 disability questions. Both sections are scored with VAS. The total score range is between 0-130 and it is calculated with the percentage score. Pain and disability are inversely proportional with the percentage score

  2. Visual Analogue Scale

    Time frame: two weeks

    to record pain intensity during rest and active shoulder movements. The patient is asked to mark the point corresponding to the pain (0 no pain and 10 maximal pain) on 10 cm horizontal line. The distance between the marked point and the beginning is recorded as a pain score

  3. Active Range of Motion measurement

    Time frame: two weeks

    Conventional goniometer with 1° increments is used to determine shoulder limitations due to pain in patients

  4. Subacromial Interval Measurement

    Time frame: six weeks

    Subacromial interval measurement was performed via anterior-posterior shoulder radiography

Sponsors and collaborators

Lead sponsor

Cukurova University

Other

Registry information

Official study title

Comparison of the Effects of Mulligan Mobilization With Movement Method and Accelerated Rehabilitation Protocol on Shoulder Pain and Functions in Subacromial Pain Syndrome: A Randomized Single Blind Trial

Important dates

Study start
2018
Primary completion
2018
Study completion
2018
First posted
Aug 15, 2019
Registry last updated
Aug 15, 2019

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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