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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03189784
Other study ID # ankle ujaen
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 15, 2018
Est. completion date April 2, 2019

Study information

Verified date December 2019
Source University of Jaén
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Ankle joint self mobilization.


Description:

The intervention would consist in the administration of self mobilization with movement techniques in patients with chronic ankle instability in addition to an exercise program


Recruitment information / eligibility

Status Completed
Enrollment 52
Est. completion date April 2, 2019
Est. primary completion date March 30, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- ankle range of motion limitation respect the contralateral ankle.

- At least two episodes of giving way on the affected ankle.

- Scores of at least 24 in the cumberland ankle instability tool.

Exclusion Criteria:

- recent fractures of the involved limb.

- Vestibular or balance dysfunction.

- Acute ankle sprain.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
mobilization with movement techniques
patient will receive an anteroposterior stimuli in the talus in order to restore the range of motion

Locations

Country Name City State
Spain University of Jaen Jaen
Spain University of Jaen campus Jaen

Sponsors (1)

Lead Sponsor Collaborator
University of Jaén

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary range of motion the ankle range of motion will be measured by goniometry. from baseline prior to the beginning of the intervention to the completion of the study at four weeks.
Secondary dynamic balance Dynamic balance will be determined by the star excursion balance test from baseline prior to the beginning of the intervention to the completion of the study at four weeks.
Secondary Self reported instability Self reported instability will be assessed by the Cumberland ankle instability tool from baseline prior to the beginning of the intervention to the completion of the study at four weeks.
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