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Exercise and Manual Therapy for Shoulder Subacromial Impingement Syndrome

NCT00632996 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 162

Last updated 2015-12-21

No results posted yet for this study

Summary

The purposes of this study are to:

1. determine if a rehabilitation program that consists of exercise and manual therapy reduces pain and improves quality of life in patients with shoulder subacromial impingement syndrome;
2. determine which patients are likely to respond to this rehabilitation program and which patients are not likely to respond to this rehabilitation program

The hypotheses are:

1. the rehabilitation treatment program will result in significant changes in pain and quality of life
2. there will be items from the history and examination that will identify those patients who respond favorably and those who do not respond favorably to rehabilitation at 6 weeks, 3, 6 and 12 months.

Conditions

  • Shoulder Impingement Syndrome

Interventions

OTHER

Rehabilitation

Exercise, manual therapy, patient education, posture, home exercise program

Sponsors & Collaborators

  • National Athletic Trainers' Association Research & Education Foundation (NATA Foundation)

    collaborator OTHER

  • University of North Florida

    collaborator OTHER

  • Arcadia University

    collaborator OTHER

  • Virginia Commonwealth University

    lead OTHER

Principal Investigators

  • Lori A Michener, PhD, PT, ATC · Virginia Commonwealth University

  • Phillip W McClure, PhD, PT · Arcadia University

  • Angela R Tate, PhD, PT · Arcadia University

  • Ian A Young, PT · Virginia Commonwealth University

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-01-31
Primary Completion
2014-01-31
Completion
2014-01-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00632996 on ClinicalTrials.gov