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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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19 February 2015 |
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Main ID: |
NCT01744002 |
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Date of registration:
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02/12/2012 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Neck Mobs and Impingement
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Scientific title:
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The Addition of Cervical Unilateral Posterior Anterior Mobilization (UPA) in the Treatment of Patients With Shoulder Impingement Syndrome: A Randomized Clinical Trial |
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Date of first enrolment:
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December 2011 |
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Target sample size:
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68 |
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT01744002 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
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Phase:
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Phase 2
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Countries of recruitment
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United States
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Contacts
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Name:
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Chad Cook, PhD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Walsh U |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Patients, age 18 and older, with shoulder impingement syndrome, who attend care at a
physical therapy outpatient setting, will be screened for eligibility for the study
by the treating physical therapists. For patients to meet inclusion requirements,
they require the following:
1. Report pain or dysfunction with elevated (overhead) arm activities, Demonstrate
pain during active shoulder movements
2. Demonstrate a positive Neer or Hawkins Kennedy Test
3. Report an onset that is non-traumatic
4. Report an onset within the last 12 months
5. Demonstrate a painful arc of movement during forward elevation of the arm from
60° to 120°
Exclusion Criteria:
- Exclusion criteria will include The presence of any red flags (i.e., tumor, metabolic
diseases, rheumatoid arthritis, osteoporosis, prolonged history of steroid use,
etc.), a history of frozen shoulder, disorders of the acromioclavicular joint,
degenerative arthritis of the glenohumeral joint, calcifying tendonitis, shoulder
instability, posttraumatic disorders, or shoulder surgery and/or elbow, hand, wrist
and blatantly misdiagnosed cervical spine disorders (e.g., cervical radiculopathy).
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Shoulder and Neck
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Intervention(s)
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Other: Shoulder treatment and neck mobilization
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Other: Control
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Primary Outcome(s)
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Quick Disabilities of Shoulder and Hand Questionaire (QuickDASH)
[Time Frame: participants will be followed for the duration of the treatment which is on average 4 weeks]
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Secondary Outcome(s)
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Numerical Pain Rating Scale (NPRS)
[Time Frame: participants will be followed for the duration of the treatment which is on average 4 weeks]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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