NCT05226611

Brief 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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
27

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Mar 2021

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 10, 2021

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 14, 2021

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 14, 2021

Completed
9 months until next milestone

First Submitted

Initial submission to the registry

January 12, 2022

Completed
26 days until next milestone

First Posted

Study publicly available on registry

February 7, 2022

Completed
Last Updated

February 7, 2022

Status Verified

January 1, 2022

Enrollment Period

1 month

First QC Date

January 12, 2022

Last Update Submit

January 25, 2022

Conditions

Keywords

CounterstrainMyotonPROTender pointsMedical Students

Outcome Measures

Primary Outcomes (1)

  • 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 Outcomes (1)

  • 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.

Study Arms (1)

Tender point treatment with Counterstrain

EXPERIMENTAL

A tender point was located in the upper trapezius region of the test subject and treated with counterstrain. The side with the highest initial pain level was used as the treatment side. Pain level was measured before and after treatment. The MyotonPRO was also used to measure physiologic parameters of the muscle before and after treatment.

Other: Counterstrain

Interventions

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.

Tender point treatment with Counterstrain

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Subject is at least 18 years of age

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

NYIT College of Osteopathic Medicine

Glen Head, New York, 11545, United States

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Masking Details
The participant felt which side was being treated however, the investigator measuring the physiologic parameters of the muscle with the MyotonPRO was blinded in terms of what side was being treated.
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 12, 2022

First Posted

February 7, 2022

Study Start

March 10, 2021

Primary Completion

April 14, 2021

Study Completion

April 14, 2021

Last Updated

February 7, 2022

Record last verified: 2022-01

Data Sharing

IPD Sharing
Will not share

Locations