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NCT01508715 · ClinicalTrials.gov registry record · NA

Comparison of Exercise Interventions in Adults With Subacromial Impingement Syndrome

A NA study, sponsored by Texas Woman's University.

Completed
Registry status
NA
Development phase
36
Enrollment target

NCT01508715: Completed NA study, sponsored by Texas Woman's University.

NCT01508715 is a NA study that has completed, run by Texas Woman's University. The registered enrollment target is 36 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01508715, a NA study, has completed, sponsored by Texas Woman's University.

COMPLETED
Registry status
NA
Development phase
36 participants
Enrollment target

Study Summary

The purpose of this study is to compare two different physical therapy exercise programs in persons who have shoulder pain in order to determine if they have a different affect on pain level and ability to use the injured shoulder after treatment. Both exercise groups will attend physical therapy for an hour,two to three times a week, for eight weeks. The first two weeks of therapy sessions will involve learning the exercises and testing to determine what weight to use during exercises. One group will perform a traditional therapy exercise program for shoulders using hand weights. The other group will perform a version of the same shoulder exercises but with a different exercise technique. Exercises in both programs are part of the standard of care for shoulder impingement in physical therapy but one program concentrates on the lowering portion of the exercise (eccentrics) while the other emphasizes the lifting portion of the exercise (concentrics). Both groups will perform the same warm-up, stretching, and cool-down exercises. Participants will also be required to perform a daily home exercise program of stretches and range of motion that will take about 20 minutes to complete. Exercise testing will determine the hand weight resistance used by each person during their therapy sessions and re-testing will occur every two weeks to determine any changes in the weight used for the exercises to keep them challenging. Pain level, ability to use the injured arm for daily activities, strength, and amount of movement in the shoulder, will be measured at the start of physical therapy and after five and eight weeks (end of study) of the exercise treatments. A concurrent study investigating the reliability of the shoulder motion and strength measurements used in the larger study will also be performed. Research hypotheses: 1. Adults with shoulder pain who complete the eccentric progressive resistive exercise intervention will demonstrate significantly greater improvements in

Primary Outcome

Measured by change in numeric pain rating scale (NPRS)score for shoulder pain, change in disabilities of the arm, shoulder, and hand (DASH) self-report of function score, change in shoulder abduction and external rotation strength assessed with a hand-held dynamometer, and change in shoulder flexion and scapular plane elevation pain-free range of motion assessed with a digital inclinometer.

Interventions

  • OTHER Shoulder resistive exercise

Trial Details

FieldValue
Enrollment Target 36 participants
Start Date 2012-02
Est. Completion 2014-04
Phase NA
Texas Woman's University

51 total trials

What the finished NCT01508715 record still lists

NCT01508715 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 36 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

The record links to 0 conditions, and to 1 intervention - of which Shoulder resistive exercise is the first listed.

NCT01508715 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01508715 about?

NCT01508715 is a clinical study titled "Comparison of Exercise Interventions in Adults With Subacromial Impingement Syndrome". The purpose of this study is to compare two different physical therapy exercise programs in persons who have shoulder pain in order to determine if they have a different affect on pain level and ability to use the injured shoulder after treatment. Both exercise groups will attend physical therapy fo...

What is the current status of trial NCT01508715?

This trial is currently completed. It is a NA study. The enrollment target is 36 participants. The study started on 2012-02. Estimated completion is 2014-04.

What interventions are being tested in trial NCT01508715?

The interventions under investigation include: Shoulder resistive exercise (OTHER).

Who is sponsoring clinical trial NCT01508715?

This trial is sponsored by Texas Woman's University, which has 51 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01508715's enrollment target sits among peer trials

36 1541st of 2000 higher than 437 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01508715, the US trial registry maintained by the National Library of Medicine. NCT01508715 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.