Exercise With Dual Task in Knee Osteoarthritis

NCT ID: NCT05280080

Last Updated: 2022-05-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

25 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-03-21

Study Completion Date

2022-05-20

Brief Summary

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The purpose of this study is to evaluate the neuromuscular and perceptual responses, pain intensity and performance in patients with severe knee osteoarthritis in a preoperative setting with low-load resistance training with a self-regulated mathematical dual-task.

Detailed Description

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Conditions

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Knee Osteoarthritis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Regular Task

Knee extensions.

Group Type ACTIVE_COMPARATOR

Resistance exercise

Intervention Type OTHER

Do the maximum number of repetitions of externally-resisted (50% 1RM) knee extensions.

Dual Task

Knee extensions while also doing a self-regulated mathematical dual-task.

Group Type EXPERIMENTAL

Resistance exercise

Intervention Type OTHER

Do the maximum number of repetitions of externally-resisted (50% 1RM) knee extensions.

Interventions

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Resistance exercise

Do the maximum number of repetitions of externally-resisted (50% 1RM) knee extensions.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* men and women above 55 years old.
* diagnosed with severe knee osteoarthritis.
* scheduled for unilateral TKA surgery in a local hospital during 2021- 2022.

Exclusion Criteria

* pain in the contralateral limb (maximum pain, ≥80 of 100 mm on a VAS during daily activities).
* another hip or knee joint replacement in the previous year.
* any medical condition in which exercise was contraindicated.
* participated in exercise programs (\>2 days/week, training at intensities of 10-15RM) in the 6 months prior to the study.
* history of stroke, brain surgery, major depression, or any self-perceived cognitive alterations that could affect the performance of dual tasks.
Minimum Eligible Age

55 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Valencia

OTHER

Sponsor Role lead

Responsible Party

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José Casaña Granell

Head of the Physiotherapy Department

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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José Casaña

Role: PRINCIPAL_INVESTIGATOR

University of Valencia

Joaquín Calatayud

Role: STUDY_CHAIR

University of Valencia

Locations

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Clinic Universitary Hospital of Valencia

Valencia, , Spain

Site Status

Countries

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Spain

Other Identifiers

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OA-22-02

Identifier Type: -

Identifier Source: org_study_id

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