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Foam Rolling: Effects of Different Densities of Foam Rollers on Passive Hip Flexion and Conditioned Pain Modulation during Self-Myofascial Release

Foam Rolling: Effects of Different Densities of Foam Rollers on Passive Hip Flexion and Conditioned Pain Modulation during Self-Myofascial Release

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00036760
Enrollment
10
Registered
2025-05-12
Start date
2025-04-18
Completion date
Unknown
Last updated
2025-10-06

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

Conditions

Study with healthy participants. Data collection regarding orthopedic questions, specifically how myofascial self-treatment using foam rollers affects mobility and conditioned pain modulation, and whether the firmness of the foam roller used plays a role in this context.

Interventions

Group 1: Three minutes of self-treatment each with a soft and a hard foam roller. 1. Pre-test: Measurement of hip joint mobility using a digital easyangle goniometer and pressure point threshold usin

Sponsors

Fascia Research Project
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: No known diseases or dysfunctions that could impede active foam rolling self-treatment of the hamstrings while seated on the floor.

Exclusion criteria

Exclusion criteria: 1. Surgery within the last three months, 2. Psychotherapeutic and/or psychiatric treatment within the last two years, 3. Major scars (2 cm in length or larger) in the area of the posterior thighs, 4. Absent or reduced perception and communication of pain, 5. Regular and long-term, as well as recent, use of pain medication, 6. Contraindications regarding self-myofascial treatment: a. Adhesions, hematomas, or skin diseases in the area of the posterior thighs, b. Acute or chronic inflammation of the muscles of the posterior thighs (redness, swelling, pain), c. Osteoporosis, d. Fibromyalgia, e. Rheumatism, f. Tumor diseases, g. Use of anticoagulant medication.

Design outcomes

Primary

MeasureTime frame
Pressure Point Threshold (PPT) at the thenar eminence, measured with the IndentoPRO Tissue Compliance Meter (Thermotrigger: Richard-Strauß-Straße 3, 85391 Allershausen) in accordance with the guidelines for "Quantitative Sensory Testing of the German Research Network on Neuropathic Pain." Measurements were taken before and after each intervention.

Secondary

MeasureTime frame
Passive hip flexion with an extended knee was measured before and after each intervention using the digital easyAngle goniometer.

Countries

Germany

Contacts

Public ContactRobert Schleip

Fascia Research Project

schleip@somatics.de+49 15228816295

Outcome results

None listed

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