Manual Therapy Versus Conventional Rehabilitation Protocol on Subacromial Pain Syndrome

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

42 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-03-01

Study Completion Date

2018-11-30

Brief Summary

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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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Detailed Description

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Conditions

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Subacromial Impingement Syndrome

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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mulligan method

Mulligan mobilization with mowement method every three days for six weeks

Group Type EXPERIMENTAL

accelerated protocol and mulligan method

Intervention Type OTHER

manual therapy technic

accelerated protocol

accelerated rehabilitation protocol every three days for six weeks

Group Type EXPERIMENTAL

accelerated protocol and mulligan method

Intervention Type OTHER

manual therapy technic

Interventions

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accelerated protocol and mulligan method

manual therapy technic

Intervention Type OTHER

Eligibility Criteria

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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

Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No