Walking Stick Exercise in Patients Underwent Total Knee Arthroplasty

NCT ID: NCT05030662

Last Updated: 2023-08-21

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

UNKNOWN

Clinical Phase

NA

Total Enrollment

88 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-08-01

Study Completion Date

2023-10-31

Brief Summary

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The purpose of this study is to examine whether the effect of "hiking poles exercise" on lower extremity muscular strength, knee range of motion, and quality of life in elderly patients underwent total knee arthroplasty

Detailed Description

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This is a longitudinal-experimental study. The data collection and analysis are in a single-blind manner. The study will be undertaken in the Department Orthopaedics of En Chu Kong hospital (approximate 500-bed regional teaching hospital). All patients who meet the inclusion criteria are admitted for primary total knee arthroplasty and assigned to control group or intervention group randomly. The 44 patients in the control group received routine guidance of " Rehabilitation and precautions for artificial knee replacement ". In addition to the routine guidance, the 44 patients in the intervention group received educations of " hiking poles exercise " on the day before surgery and before discharge, as well as a follow-up call at least once a week after discharge.

Conditions

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Arthroplasty Replacement Knee Osteoarthritis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants
Sigle,were not involved in the study assessments beyond recording the timed-get-up-and-go test before and after the treatment intervention

Study Groups

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Experimental:Walking stick exercise

The experimental:Walking stick exercise

1. Education of walking stick exercise by research nurses twice before discharge (on the day before surgery and before discharge)
2. The video clip of "walking stick exercise" is available to the patients.
3. The research nurses encourage our patients to keep rehabilitation by phone calls once a week after discharge.

Group Type EXPERIMENTAL

Walking stick exercise

Intervention Type OTHER

1. Education of walking stick exercise by research nurses twice before discharge (on the day before surgery and before discharge)
2. The video clip of "walking stick exercise" is available to the patients.
3. The research nurses encourage our patients to keep rehabilitation by phone calls once a week after discharge.

Control group: conventional physical therapy.

1. Perform bed mobility and transfers with the least amount of assistance while maintaining appropriate weight bearing (WB) precautions.
2. Ambulate with an assistive device for 25-100 feet and ascend/descend stairs to allow for independence with household activities while maintaining appropriate WB.
3. Verbalize understanding of post-operative activity recommendations/precautions including use of proper positioning of the lower extremity, range of motion and strengthening exercises.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Walking stick exercise

1. Education of walking stick exercise by research nurses twice before discharge (on the day before surgery and before discharge)
2. The video clip of "walking stick exercise" is available to the patients.
3. The research nurses encourage our patients to keep rehabilitation by phone calls once a week after discharge.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Age between 60 and 85 years
* Informed consent
* Receipt of elective unilateral primary knee arthroplasty surgery.

Exclusion Criteria

* Non-degenerative arthritis, including rheumatoid arthritis, or traumatic arthritis
* Patients receiving rehabilitation simultaneously
* Patients with other musculoskeletal or neurological problems, including fractures, Parkinsonism, cerebrovascular events, or patients with multiple comorbidities
* Cancer patients receive chemotherapy
* Patients with the peri-operative complication that has an adverse effect on outcomes,for example: intra-operative fractures, thromboembolism, peri-operative infections, or phlebitis
Minimum Eligible Age

60 Years

Maximum Eligible Age

85 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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National Taipei University of Nursing and Health Sciences

OTHER

Sponsor Role lead

Responsible Party

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Yu Hua Chou

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Yu Hua Chou

Role: PRINCIPAL_INVESTIGATOR

none,specify Unaffiliated

Locations

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TAIWAN

New Taipei City, , Taiwan

Site Status

Countries

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Taiwan

Provided Documents

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Document Type: Study Protocol and Informed Consent Form

View Document

Other Identifiers

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YChou

Identifier Type: -

Identifier Source: org_study_id

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