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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06398184
Other study ID # MI1
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date May 15, 2024
Est. completion date December 15, 2024

Study information

Verified date April 2024
Source Cardenal Herrera University
Contact Luis Suso-Martí, PhD
Phone 627819667
Email luis.suso@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The main objective of this study is to evaluate the effects of an exercise programme combined with motor imagery and action observation, both in the short and long term.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 40
Est. completion date December 15, 2024
Est. primary completion date October 15, 2024
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - diagnosed with severe knee OA (according to the clinical and radiographic criteria of the American College of Rheumatology Guidelines) Exclusion Criteria: - pain in the contralateral (non-studied) limb (maximum =80 of 100 mm on a visual analog scale (VAS) during daily activities), - undergone another hip or knee joint replacement in the previous year - any medical condition in which exercise was contraindicated or if they had participated in exercise programs or motor imagery/action observation intervention

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Exercise + motor imagery and action observation
A total of 8 sessions of 4 sets of knee extension exercises will be performed. During the breaks between each series, participants will perform a progressive protocol of action observation and motor imagery.
Exercise
A total of 8 sessions of 4 sets of knee extension exercises will be performed.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Cardenal Herrera University

Outcome

Type Measure Description Time frame Safety issue
Primary Pain intensity (Visual analogue scale) Pain intensity will be measured using a visual analogue scale. through study completion, 1 month
Primary Disability (WOMAC scale) Disability will be measured using WOMAC scale. through study completion, 1 month
Primary Algometry Pressure pain thresholds will be measured by algometry on the affected knee, contralateral knee and epicondyle. through study completion, 1 month
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