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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02552290
Other study ID # 1303-4412
Secondary ID
Status Completed
Phase N/A
First received September 14, 2015
Last updated September 16, 2015
Start date November 2013
Est. completion date November 2014

Study information

Verified date September 2015
Source University of Nevada, Las Vegas
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The proposed project seeks to evaluate the influence of cervicothoracic (CT) manipulation and passive stretching to the upper trapezius on pressure pain thresholds and range of motion (ROM) in individuals without recent complain of neck pain.


Description:

Not needed


Recruitment information / eligibility

Status Completed
Enrollment 90
Est. completion date November 2014
Est. primary completion date November 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

1. No current history or past history of neck pain; able to lie on back or stomach without difficulty

Exclusion Criteria:

1. 'Red flag' items indicated in your Neck Medical Screening Questionnaire such as history of a tumor, bone fracture, metabolic diseases, Rheumatoid Arthritis, osteoporosis, severe atherosclerosis, prolonged history of steroid use, etc.

2. History of neck whiplash injury

3. Diagnosis from your physician of cervical spinal stenosis (narrowing of spinal canal) or presence of symptoms (pain, pins and needles, numbness) down both arms

4. Presence of central nervous system involvement such as exaggerated reflexes, changes in sensation in the hands, muscle wasting in the hands, impaired sensation of the face, altered taste, and presence of abnormal reflexes

5. Evidence of neurological signs consistent with nerve root entrapment (pinched nerve in the neck)

6. Prior surgery to your neck or upper back

7. A medical condition which may influence assessment of pain or pressure pain thresholds (i.e. taking analgesics, sedatives, history of substance abuse, or cognitive deficiency)

8. Diagnosis from your physician of fibromyalgia syndrome

9. Currently pregnant, or could be pregnant

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Other:
Upper Trapezius Stretch
Sustained stretch of upper trapezius muscle
Cervicothoracic manipulation
Manipulation to the cervicothoracic spine
No intervention
Wait

Locations

Country Name City State
United States University of Nevada Las Vegas - Department of Physical Therapy Las Vegas Nevada

Sponsors (1)

Lead Sponsor Collaborator
University of Nevada, Las Vegas

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Cervical Range of Motion Cervical Range of Motion in each cardinal plane (sagittal, coronal and transverse) will be measured in angular degrees using a CROM device Immediately after the intervention No
Secondary Pain Pressure Threshold Pain Pressure Threshold measured using a standard handheld algometer with 1 cm round tip Two minutes and 5 Minutes after the intervention No
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