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Investigation of the effect of a myofascial release technique on the thoracolumbar fascia

Investigation of the effect of a myofascial release technique on the thoracolumbar fascia - myof-TLF

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00032209
Enrollment
20
Registered
2023-07-18
Start date
2023-03-09
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy patients

Interventions

Group 1: First application of a placebo treatment, then application of the myofascial treatment, with 3 minutes of active break in between. The myofascial treatment consists of a slow massage of the l
3x in cranial direction parallel to the spine on each side of the back. In the placebo treatment, the same skin areas are touched only with a fingertip, while the same hand holds a Sham laser pen that
while the practitioner and patient each wear laser safety goggles. For both treatments, the patient lies in a prone position. Group 2: First application of a myofascial treatment, then application of
while the practitioner and patient each wear laser safety goggles. For both treatments, the patient lies in a prone position.

Sponsors

Fascia Research Project
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Healthy clients

Exclusion criteria

Exclusion criteria: Patients must have no contraindication to myofascial treatment. Additional exclusion criteria include pregnancy, use of pain medication or medication containing cortisone, history of spinal surgery, and rheumatic diseases. Patients - but not practitioners or evaluators - are blinded to the presumed mechanical efficacy of the two treatment procedures.

Design outcomes

Primary

MeasureTime frame
Measurement of the stiffness of the skin with a durometer, 4 cm lateral to L3. 2) Measurement of the stiffness as well as the elastic recovery capacity of the myofascial tissues close to the skin with an IndentoPro measuring device, 4 cm lateral to L3. 3) Measurement of the pressure pain threshold (Pressure Pain Threshhold) with an Algometer 4 cm lateral to L2. 4) These measurements are applied to both sides of the body (right/left) and are conducted directly before and directly after each of the two interventions.

Secondary

MeasureTime frame
Measurement of active lumbar flexion ability using the modified Schober test.

Countries

Germany

Contacts

Public ContactRobert Schleip

Fascia Research Project

schleip@somatics.de015228816295

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026