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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03521544
Other study ID # P1/01
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 16, 2018
Est. completion date May 18, 2018

Study information

Verified date June 2018
Source Universitat Internacional de Catalunya
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study investigates the relation between different segments of the posterior myofascial chain of the human body.

The intervention consists on apply self-myofascial release with a foam roller in one of the segments of the posterior myofascial chain of the participants, and then see if the treatment has produced any changes in the hamstrings, gastrocnemius and soleus flexibility.


Description:

The study investigates the relation between different segments of the posterior myofascial chain of the human body.

The intervention consists on apply self-myofascial release with a foam roller in one of the segments of the posterior myofascial chain, and then see if the treatment has produced any changes in the hamstrings, gastrocnemius and soleus flexibility.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date May 18, 2018
Est. primary completion date May 18, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility Exclusion Criteria:

- Pregnant women

- Musculoskeletal problems in the last month

- Surgical interventions in he knee, hip, ankle, back or neck in tha last 6 months

- Psychological or nervous alterations

- Uncomprehension of the study protocol

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Self-myofascial release
The subjects roll a foam roller under a determinated part of the body to self-massage that area.

Locations

Country Name City State
Spain Universitat Internacional de Catalunya Sant Cugat Del Vallès Barcelona

Sponsors (1)

Lead Sponsor Collaborator
Universitat Internacional de Catalunya

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Hamstrings flexibility change Measurement of the hamstrings flexibility change through Sit and Reach Test 0 seconds, 30 seconds, 2 minutes, 5 minutes, 10 minutes
Secondary Triceps surae flexibility change Measurement of the triceps surae flexibility change using the Lunge Test. 0 seconds, 10 minutes
Secondary Fatigue Fatigue subjective sensation using the Modified Borg Scale 10 minutes