- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01518504
Effects of Thoracic Mobilization on Shoulder Range of Motion
Study Overview
Status
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Nebraska
-
Omaha, Nebraska, United States, 68178
- Creighton University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Adults 19-45 years
Exclusion Criteria:
- Individuals who are pregnant
- History of cervical or thoracic surgery
- Bone or joint disease
- Current infection or tumor
- Osteopenia/osteoporosis
- Spinal fracture
- Rheumatologic pathologies
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Thoracic Mobilization
The subject will be in a prone position and the physical therapist will first identify the upper thoracic spine region.
The physical therapist will then cross his or her hands and place them on opposite sides of the spinous processes using the pisiforms as the contact area.
The subject will be asked to exhale and upon exhalation the physical therapist will apply a small amplitude, quick thrust at end of range.
|
The subject will be in a prone position and the physical therapist will first identify the upper thoracic spine region.
The physical therapist will then cross his or her hands and place them on opposite sides of the spinous processes using the pisiforms as the contact area.
The subject will be asked to exhale and upon exhalation the physical therapist will apply a small amplitude, quick thrust at end of range.
Other Names:
|
Sham Comparator: Sham
The subject will be in a prone position and the physical therapist will first identify the upper thoracic spine region.
The physical therapist will then cross his or her hands and place them on opposite sides of the spinous processes using the pisiforms as the contact area.
The subject will be asked to exhale and upon exhalation the physical therapist will not apply any other force than light hand contact.
|
The subject will be in a prone position and the physical therapist will first identify the upper thoracic spine region.
The physical therapist will then cross his or her hands and place them on opposite sides of the spinous processes using the pisiforms as the contact area.
The subject will be asked to exhale and upon exhalation the physical therapist will not apply any other force than light hand contact.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Changes in Shoulder Range of motion
Time Frame: Single Study Visit
|
To determine changes in shoulder active and passive range of motion following one of two intervention protocols. Changes will be measured by examining shoulder range of motion in three directions: Shoulder flexion, internal rotation and external rotation. We hypothesize that the use of a thoracic spine joint manipulation will increase shoulder range of motion in flexion (elevation) as well as external and internal rotation to a greater degree than a sham mobilization. |
Single Study Visit
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Terry L Grindstaff, PHD,PT,ATC, Creighton University
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 11-16286
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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