Blood Flow Within Active Myofascial Trigger Points Following Massage

Sponsor
University of Colorado, Denver (Other)
Overall Status
Completed
CT.gov ID
NCT02389140
Collaborator
(none)
28
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2
22.1
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Study Details

Study Description

Brief Summary

The physiological response at the myofascial trigger point (MTrP) to massage is not known, yet would provide important objective evidence for a treatment effect and clarify the resolution process of a MTrP.

Condition or Disease Intervention/Treatment Phase
  • Other: Trigger point release
  • Other: Ultrasound
N/A

Detailed Description

The physiological response at the myofascial trigger point (MTrP) to massage is not known, yet would provide important objective evidence for a treatment effect and clarify the resolution process of a MTrP. The long-term goal is to understand how therapeutic intervention affects the physiology of the MTrP. The objective of the proposed research is to assess, in a placebo controlled trial, the effectiveness of trigger point release massage (also known as ischemic compression) on blood flow at an active MTrP. The central hypothesis is that the contraction nodule of an active MTrP is characterized by an ischemic state comprised of reduced blood flow and subsequent dysregulation in carbohydrate metabolism. The investigators hypothesize that trigger point release (TPR) can positively impact blood flow leading to a change in high energy carbohydrate tension. The present study has been formulated, in part, from a preliminary study conducted by the investigators, which supports reduced blood flow and physiological disruption at active MTrPs. The proposed research will provide a physiological basis for massage to corroborate subjective reports of reduced pain sensitivity, impart credibility to treatment techniques, and provide insight into a mechanism of action for healing the MTrP.

Study Design

Study Type:
Interventional
Actual Enrollment :
28 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Other
Official Title:
Blood Flow Within Active Myofascial Trigger Points Following Massage
Study Start Date :
Mar 1, 2015
Actual Primary Completion Date :
Dec 1, 2016
Actual Study Completion Date :
Jan 1, 2017

Arms and Interventions

Arm Intervention/Treatment
Experimental: Trigger point treatment

Trigger point release

Other: Trigger point release
Trigger point therapy

Sham Comparator: Ultrasound

Sham US at Trigger point

Other: Ultrasound
sham ultrasound

Outcome Measures

Primary Outcome Measures

  1. Change in Blood Flow as measured by microdialysis [1 hr pre intervention and 1 hr post intervention]

Secondary Outcome Measures

  1. Change in Glucose as measured by microdialysis [1 hr pre intervention and 1 hr post intervention]

  2. Change in Lactate as measured by microdialysis [1 hr pre intervention and 1 hr post intervention]

  3. Change in Pyruvate as measured by microdialysis [1 hr pre intervention and 1 hr post intervention]

Eligibility Criteria

Criteria

Ages Eligible for Study:
21 Years to 49 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Chronic or episodic tension-type headache

  • active MTrP in upper trapezius

  • age 21-49

  • BMI between 18.5-24.9

  • either gender

  • any race or ethnicity

Exclusion Criteria:
  • No or latent MTrP in the upper trapezius

  • migraine 4+/month

  • cluster headache

  • fibromyalgia

  • neurological disease (e.g. Alzheimer's disease, Parkinson's disease, muscular dystrophy, multiple sclerosis)

  • cardiovascular disease (e.g. prior heart attack or stroke)

  • diabetes

  • pregnancy

  • a bleeding disorder (Self-report of hemophilia, known lack/deficiency of clotting factors, or presently °taking anti-coagulants (e.g. warfarin, Coumadin))

  • narcotic use

  • currently receiving massage

  • prior trigger point injection or needling therapies

  • allergy to lidocaine-type anesthetics such as lidocaine and prilocaine

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Colorado Hospital Aurora Colorado United States 80045

Sponsors and Collaborators

  • University of Colorado, Denver

Investigators

  • Principal Investigator: Albert Moraska, PhD, University of Colorado, Denver

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Colorado, Denver
ClinicalTrials.gov Identifier:
NCT02389140
Other Study ID Numbers:
  • 14-1582
  • UL1TR001082
First Posted:
Mar 17, 2015
Last Update Posted:
Sep 1, 2017
Last Verified:
Aug 1, 2017
Keywords provided by University of Colorado, Denver
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 1, 2017