Community Based Rehabilitation Model After Total Knee Replacement

NCT ID: NCT06270446

Last Updated: 2024-02-21

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

COMPLETED

Clinical Phase

NA

Total Enrollment

59 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-01-01

Study Completion Date

2022-07-01

Brief Summary

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To investigate the clinical efficacy of community-based early stage knee replacement rehabilitation program as compared with usual care in acute hospital outpatient clinic

Detailed Description

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To investigate the clinical efficacy of community-based early stage knee replacement rehabilitation program as compared with usual care in acute hospital outpatient clinic

Conditions

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Knee Osteoarthritis

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Data analysis blinded

Study Groups

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Outpatient

Usual care, outpatient physiotherapy

Group Type OTHER

Outpatient physiotherapy

Intervention Type OTHER

Physiotherapy at hospital

CRC

Community based physiotherapy

Group Type ACTIVE_COMPARATOR

Community based physiotherapy

Intervention Type OTHER

Physiotherapy at community rehabilitation center

Interventions

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Community based physiotherapy

Physiotherapy at community rehabilitation center

Intervention Type OTHER

Outpatient physiotherapy

Physiotherapy at hospital

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

i) unilateral TKA; ii) age 55 years old and above; iii) able to engage in outpatient physiotherapy; iii) postoperative knee flexion ≥75° and knee extension ≤5°; iv) able to ambulate independently preoperatively.

Exclusion Criteria

i) had revision TKA or fully constrained knee arthroplasty; ii) had knee replacement for indications other than osteoarthritis; iii) had post-operative complications during hospital stay; iv) were unable to participate due to cognitive impairment or language barriers; v) had acute spinal diseases or joint, muscle or systemic diseases affecting gait; iv) had comorbid health conditions that would prevent active participation (e.g. prior hemiplegic stroke, severe cardiorespiratory illnesses.
Minimum Eligible Age

55 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Tan Tock Seng Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Eng Chuan Neoh

Role: PRINCIPAL_INVESTIGATOR

Tan Tock Seng Hospital

Locations

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Tan Tock Seng Hospital

Singapore, , Singapore

Site Status

Countries

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Singapore

Other Identifiers

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DSRB 2019/01135

Identifier Type: -

Identifier Source: org_study_id

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