The effect of a foam rolling self-treatment on Conditioned Pain Modulation (CPM)

Not Applicable

• Conditions: Pressure pain sensitivity; hip joint mobility

• Registration Number: DRKS00032054
• Lead Sponsor: Fascia Research Project

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2023-06-13
• Study Completion: 2023-06-30
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 34

Inclusion Criteria

No additional inclusion criteria

Exclusion Criteria

Patients who have severe orthopedic, cardiovascular, pulmonary, neurological, psychiatric or inflammatory rheumatic diseases, who are pregnant or lactating, who have taken pain medication in the last 48 hours, or who have had surgery or trauma to the lower extremity cannot participate in the study. Furthermore, patients suffering from poor sleep quality will be excluded from the study.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pressure pain threshold (PPT) at the thenar prominence, measured with Algometer FDN 300 from Wagner Instruments (Greenwich, CT 06836-1217 USA) according to the guidelines for Quantitative Sensory Testing of the German Neuropathic Pain Research Association. Measurement before and after each intervention. <br>

Secondary Outcome Measures

Name	Time	Method
Passive Range of Motion (ROM) of hip joint with extended knee before and after each intervention, assessed with EasyAngle digital goniometer.