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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05153993
Other study ID # 2017/1215
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 1, 2017
Est. completion date May 5, 2018

Study information

Verified date November 2021
Source University Ghent
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

RCT with two arms: (1) stretch fascia plantaris (6 weeks, n=30) (2) control (n=30); Outcome parameters: ROM ankle and first toe; visco-elastic behaviour of the fascia plantaris determined by means of myotonometry Study protocol: Outcome parameters were evaluated before and after the intervention/control with a 6 weeks interval. All participants were screened bilaterally and for the participants assigned to the intervention group stretching was only performed on the dominant side


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date May 5, 2018
Est. primary completion date December 20, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Healthy volunteers Exclusion Criteria: - Lower extremity injury

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Fascia stretch
Stretch of the fascia plantaris during 3x30", 5x/week, 6 weeks

Locations

Country Name City State
Belgium Roel De Ridder Ghent East Flanders

Sponsors (1)

Lead Sponsor Collaborator
University Ghent

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Visco-elastic behaviour using myotonometry By means of the MyotonPro device within 20 minutes before and after intervention
Secondary Range of Motion of ankle joint and first metatarsalphalangeal joint By means of goniometry within 20 minutes before and after intervention
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