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Prehabilitation Effect on Function and Patient Satisfaction Following Total Knee Arthroplasty

NCT ID: NCT05892133

Last Updated: 2023-12-15

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

RECRUITING

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-09-05

Study Completion Date

2030-12-31

Brief Summary

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Knee arthrosis has a high prevalence. Non-surgical treatment, such as exercise, is the first choice of treatment. However, most patients end up having a surgical procedure such as total knee arthroplasty. Following surgery with total knee replacement as much as 20% of patients report to not be satisfied with the results. It is noteworthy that this level of dissatisfaction has persisted over the last decades despite formidable progress in surgical methods and technology. Leg strength prior to surgery is associated with faster recovery post operatively, which may influence satisfaction. The investigators aim is to implement a period of strength training prior to surgery to evaluate if training prior to surgery may reduce the level of dissatisfaction post operatively.

Detailed Description

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Conditions

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Prehabilitation Knee Osteoarthritis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors

Study Groups

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Maximal strength training

eight weeks of leg press strength training prior to knee surgery

Group Type EXPERIMENTAL

Maximal strength training

Intervention Type BEHAVIORAL

3 sessions/ week. leg press at \~85% of one repetition maximum for 8 weeks

Control

treatment as usual prior to knee surgery

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Maximal strength training

3 sessions/ week. leg press at \~85% of one repetition maximum for 8 weeks

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Knee artrosis, refered to surgery

Exclusion Criteria

* Kognitive disability
* Inflamatory disease in muscles
* varus/ valgus and extension deficit \>15 degrees
* Neurological disorders
Minimum Eligible Age

50 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Molde University College

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Berg

Role: PRINCIPAL_INVESTIGATOR

Molde UC

Locations

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Molde University College

Molde, Møre og Romsdal, Norway

Site Status RECRUITING

Countries

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Norway

Central Contacts

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Berg

Role: CONTACT

Phone: +47 71 19 57 71

Email: [email protected]

Facility Contacts

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Ole Kristian Berg, Dr.

Role: primary

Other Identifiers

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522685

Identifier Type: -

Identifier Source: org_study_id