Immediate Effects Cervicothoracic Manipulation Versus Passive Upper Trapezius Stretch

NCT ID: NCT02552290

Last Updated: 2015-09-17

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 90 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2013-11-30
• Study Completion Date: 2014-11-30

Brief 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.

Detailed Description

Not needed

Conditions

Neck Pain

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Cervicothoracic manipulation

Description of a Right C7/T1 manipulation. The subject will lie prone. The therapist will stand on the L side of the subject facing in a cephalic direction (towards the patient's head). The therapist's right hand makes contact with the thumb on the right side of the spinous process of the first thoracic vertebra. The therapist left hand supports the head making contact on the temporal bone. The hand/neck is gently laterally flexed to the right, until slight tension is palpated in the tissues. A high-velocity low-amplitude thrust will be applied towards the subjects left side. If cavitation does not occur (an audible pop) the subject will be repositioned and the manipulation attempted a second time. A maximum of 2 attempts will be performed for each side of the neck.

Group Type: ACTIVE_COMPARATOR

Cervicothoracic manipulation

Intervention Type: OTHER

Manipulation to the cervicothoracic spine

Upper trapezius stretch

The subjects will be in a supine position. A researcher will passively place the subject's head into flexion, side-bending away and rotation towards the side to be stretched until the muscle barrier is met. The researcher will depress the subject's shoulder with 100 Newtons of force measured with a Micro FET pressure dynamometer (Hoggan Health Industries, Salt Lake City, UT).) Once this pressure amount is achieved the stretch will be held for 30 seconds. This will be repeated two times on each side.

The subject will be asked to provide continuous feedback about the stretch felt and the degree of discomfort (if any) felt during the 30 second stretches.

Group Type: ACTIVE_COMPARATOR

Upper Trapezius Stretch

Intervention Type: OTHER

Sustained stretch of upper trapezius muscle

Control group

Subjects assigned to the control group will receive no intervention. They will stay behind the curtained research area for approximately 3 minutes in a seated position.

Group Type: OTHER

No intervention

Intervention Type: OTHER

Wait

Interventions

Upper Trapezius Stretch

Sustained stretch of upper trapezius muscle

Intervention Type: OTHER

Cervicothoracic manipulation

Manipulation to the cervicothoracic spine

Intervention Type: OTHER

No intervention

Wait

Intervention Type: OTHER

Eligibility Criteria

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

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

University of Nevada, Las Vegas

OTHER

Sponsor Role: lead

Responsible Party

Emilio J Puentedura, PT, DPT, PhD

Associate Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Emilio J Puentedura, PT, DPT, PhD

Role: PRINCIPAL_INVESTIGATOR

UNLV

Locations

University of Nevada Las Vegas - Department of Physical Therapy

Las Vegas, Nevada, United States

Countries

United States

Other Identifiers

1303-4412

Identifier Type: -

Identifier Source: org_study_id