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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05226611
Other study ID # #BHS-1561
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 10, 2021
Est. completion date April 14, 2021

Study information

Verified date January 2022
Source New York Institute of Technology
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Medical students are prone to developing neck pain due to prolonged studying and poor posture. This can manifest as tender points in the upper trapezius region. Counterstrain (CS) is an osteopathic manipulative technique that has shown efficacy in previous studies in treating tender points. The MyotonPRO is a myotonometric device that can be used to measure various muscle parameters such as muscle stiffness. There is limited research regarding the use of osteopathic manipulative medicine to produce measurable changes in muscle stiffness by the MyotonPRO. This educational study aims to establish the efficacy of CS technique in decreasing the pain level of upper trapezius tender points in medical students as well as determining if CS causes a significant decrease in muscle stiffness in treated tender points as measured by the MyotonPRO. The investigators hope this educational study will encourage further studies on how osteopathic manipulative techniques affects the physiologic parameters of muscles.


Recruitment information / eligibility

Status Completed
Enrollment 27
Est. completion date April 14, 2021
Est. primary completion date April 14, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Subject is at least 18 years of age Exclusion Criteria: - Traumatized (sprained or strained) tissues, which would be negatively affected by the positioning of the patient - Illness or other conditions in which strict positional restrictions preclude treatment - Instability of the area being positioned that has the potential to produce unwanted neurologic or vascular side effects - Vascular or neurologic syndromes, such as basilar insufficiency or neural foraminal compromise whereby the position of treatment has the potential to exacerbate the condition - Severe degenerative spondylosis with local fusion and no motion at the level where treatment positioning would normally take place - Pregnancy - Positive for COVID-19 as well as symptoms indicating a SARS-CoV-2 infection

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Counterstrain
Counterstrain is a hands-on OMM technique that involves shortening the muscle to resolve the dysfunctional muscle stretch reflex and holding it for 90 seconds. The patient is then brought back to a neutral position and reassessed.

Locations

Country Name City State
United States NYIT College of Osteopathic Medicine Glen Head New York

Sponsors (1)

Lead Sponsor Collaborator
New York Institute of Technology

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain level Pain level of the tender point as rated by the test subject out of a scale of 1 to 10, 1 being very little pain and 10 being the most pain the test subject has ever felt. This was done immediately before and immediately after counterstrain treatment. Counterstrain treatment is a hands-on osteopathic manipulative technique that involves shortening the muscle belly of the painful region.
Secondary Muscle Stiffness Muscle stiffness measured by the MyotonPRO, a myotonometric device that applies a brief mechanical impulse to the targeted muscle, used to measure physiologic parameters such as muscle stiffness. This was done immediately before and immediately after counterstrain treatment. Counterstrain treatment is a hands-on osteopathic manipulative technique that involves shortening the muscle belly of the painful region.
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