Immediate Effects of Self-myofascial Release on Latent Trigger Point Sensitivity

Not Applicable

Completed

• Conditions: Trigger Points

• Registration Number: NCT02609412
• Lead Sponsor: Goethe University

Brief Summary

Latent myofascial trigger points (LMTRP) which impair neuromuscular performance occur in both, patients and asymptomatic subjects. As evidence suggests that LMTRP can transform into active trigger points, therapy seems warranted. Besides other modalities, self-massage using foam rollers (self-myofascial release) has been applied as a treatment. However, there is no data on the efficacy of this method concerning LMTRP. Thus, the present study aims to evaluate the effects of different forms of self-myofascial release on LMTRP pain.

Healthy patients with LMTRP in the calf are randomly allocated to one of three groups: 1) 90s static compression of the most sensitive LMTRP by means of the foam roll, 2) dynamic self-myofascial release rolling back and forth on the calf muscles for 90s using a foam roller, 3) placebo laser acupuncture of the most sensitive LMTRP. All subjects participate in a familiarization session with the foam roller one week prior to treatments. As an outcome, pressure pain threshold is assessed with an algometer. The investigators hypothesize, that static compression can reduce pressure pain of LMTRP more effective than dynamic self-myofascial release. The investigators further expect that placebo treatment will be the least effective method.

Detailed Description

Not available

Study Timeline

• Study Start: 2015-05
• Study First Submitted: 2015-10-02
• Study First Submitted QC: 2015-11-18
• Study First Posted: 2015-11-20
• Status Verified: 2016-05
• Primary Completion: 2016-05
• Study Completion: 2016-05
• Last Update Submitted: 2016-05-10
• Last Update Posted: 2016-05-11

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 48

Inclusion Criteria

• at least one diagnosed latent myofascial trigger point in the calf
• age 18 to 65 years
• written informed consent

Exclusion Criteria

• active myofascial trigger point in the calf
• regular intake of drugs or within past 48 hours
• severe psychiatric, neurological, orthopaedic, cardiovascular or endocrine diseases
• pregnancy or nursing period
• any condition that negatively influences current quality of life

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Change in pressure pain threshold [kg/cm²] assessed by pressure algometer	Baseline (M1) - 3 minutes (M2)

Trial Locations

Locations (1)

Goethe University Frankfurt/Main; 🇩🇪 Frankfurt/Main, Germany