Progressive Exercise After Total Knee Arthroplasty (TKA)

NCT ID: NCT00605124

Last Updated: 2013-03-05

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

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

120 participants

Study Classification

INTERVENTIONAL

Study Start Date

2008-01-31

Study Completion Date

2012-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Total knee arthroplasty (TKA) is performed more than 7.000 times a year in Finland most often for osteoarthritis (OA). While pain is predictably reduced, function does not typically ever reach that of age-matched, uninjured subjects. Quadriceps weakness has been implicated in the development and progression of knee OA and is a significant problem after TKA. Advance to return to normal daily activities is not sufficient to restore knee function or quadriceps strength after TKA.

The aim of this study is to assess the effectiveness of progressive exercise program restoring knee strength, mobility and improving the functional outcome after primary TKA.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Many studies have shown, that after TKA pain decreased significantly, but muscle strength of the operated knee did not recover and may stay under the preoperative level. To find out the effects of progressive exercise program the investigators will perform, 6 weeks after TKA, a randomized clinical trial of lower extremity strength training using two subgroups of people: traditional exercise group and progressive exercise group.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Osteoarthritis

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Investigators Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

exercise

progressive exercise, home-based exercise program, tree exercise sessions weekly, chec-up visits every third month

Group Type EXPERIMENTAL

Knee muscle exercises

Intervention Type OTHER

Home exercises three times a week, control every three months

Conventional treatment

Normal treatment, single guidance to home exercise

Group Type ACTIVE_COMPARATOR

Knee muscle exercises

Intervention Type OTHER

Home exercises three times a week, control every three months

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Knee muscle exercises

Home exercises three times a week, control every three months

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* primary unilateral TKA for knee osteoarthritis

Exclusion Criteria

* Rheumatoid arthritis
* Fibromyalgia
* Bilateral TKA
* Heart or lung disease, which prevent training
* Unstable serious disease (cancer)
* Reduced cooperation (drug, alcohol abuse, mental illness)
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Jyväskylä Central Hospital

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Mirja Vuorenmaa

physiotherapist

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Jari Ylinen, MD, PhD

Role: STUDY_DIRECTOR

Central Finland Health Care District

Arja Häkkinen, PhD, Professor

Role: STUDY_CHAIR

Central Finland Health Care District

Petri Salo, M.Sc.

Role: PRINCIPAL_INVESTIGATOR

Central Finland Health Care District

Mirja Vuorenmaa, M.Sc.

Role: PRINCIPAL_INVESTIGATOR

Central Finland Health Care District

Maija Pesola, MD

Role: STUDY_CHAIR

Central Finland Health Care District

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Ceneral Finland Health Care District

Jyväskylä, , Finland

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Finland

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

KSSHP

Identifier Type: OTHER

Identifier Source: secondary_id

KSSHP Dnro6/2007

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Knee Arthroplasty Activity Trial
NCT04107649 ACTIVE_NOT_RECRUITING NA
Muscle Recovery After Total Knee Arthroplasty
NCT06096792 ACTIVE_NOT_RECRUITING
PNF Stretching for TKA on ROM
NCT00797875 UNKNOWN NA