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Effectiveness of a Community-based Multi-modal Tai Chi Rehabilitation Program for Patients After Total Knee Arthroplasty

Acceptability and Feasibility of a Community-based Strength, Balance and Tai Chi Rehabilitation Program in Improving Physical Function and Balance of Patients After Total Knee Arthroplasty: a Pilot Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03565380
Enrollment
53
Registered
2018-06-21
Start date
2018-11-11
Completion date
2021-08-30
Last updated
2022-03-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Total Knee Arthroplasty

Keywords

Tai Chi, Lower limb muscle strength, Balance, Rehabilitation, Multi-faceted intervention

Brief summary

The rate of falls in patients after total knee arthroplasty (TKA) is high and related to lower limb muscle weakness and poor balance control. However, since routine post-TKA rehabilitation is uncommon, it is paramount to explore alternative strategies to enhance balance and physical functioning in post-TKA patients. As Tai Chi is a proven strategy for improving balance in older people, the proposed study aims to determine the feasibility and acceptability of a 12-week community-based post-TKA multimodal Tai Chi program and to collect preliminary data with respect to the efficacy of such a program in improving balance and physical functioning in post-TKA patients as compared to usual postoperative care.

Detailed description

This is a single-blinded 2-arm RCT. TKA participants will be randomized to either a 12-week community-based rehabilitation program starting at 12 weeks after TKA, or usual post-operative care without outpatient physiotherapy. A third group of asymptomatic controls will be recruited to provide comparisons at various time points. All post-TKA participants will undergo five clinical assessments: 1 week before TKA, and at 6, 12, 24 and 52 weeks after TKA. The untreated asymptomatic controls will be assessed at baseline, and 12 and 52 weeks from baseline

Interventions

OTHER12-week community-based multi-model Tai Chi rehabilitation program

Participants will receive 12 x 90 minute sessions of supervised exercises over 12 weeks. In addition to usual care, supervised exercise will be held at the Center of Sports Training and Rehabilitation inside the University and each class will be restricted to no more than 8 participants to ensure sufficient personalized attention. Each training session involves warm-up together with stretching of lower extremity muscles, strengthening exercises of the major lower extremity muscle groups by Theraband, balancing exercise, Tai Chi training, and rest/ cool-down. All lower-extremity exercises will be performed bilaterally.

No intervention will be provided

OTHERUntreated asymptomatic controls

No intervention will be provided

Sponsors

The Hong Kong Polytechnic University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Masking description

The reassessments at 6-, 12-, 24-, and 52 weeks, and prospective falls evaluation will be conducted by assessors blinded to group allocation. Due to the nature of the trial, the certified Tai Chi instructor who provides treatments and participants will not be blinded to group allocation.

Eligibility

Sex/Gender
ALL
Age
60 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

1. 60 years or above; 2. candidates for primary unilateral TKA who are placed on the TKA waiting list for less than 1 month before their surgery; 3. living independently in the community

Exclusion criteria

1. living in assisted living facilities, requiring nursing care, or planning to reside away from the hospital district within 1 year. 2. unstable medical conditions, 3. fracture of lower limbs, 4. malignancy in the last five years, 5. lower limb prosthesis/amputation, 6. congenital defect that is considered to cause the present complaint, 7. systemic inflammatory and autoimmune diseases, 8. previous osteotomy, 9. neurological diseases (e.g. Parkinson's disease, stroke), 10. blindness, revision TKA, 11. complications after primary TKA, 12. cognitive impairment with a Mini-Mental State Examination score \< 19 13. prior experience in practicing Tai Chi exercise for at least 3 months

Design outcomes

Primary

MeasureTime frameDescription
Rate of recruitment and rate of retentionAfter 52 week post-TKA follow-upThe recruitment and attrition rates will be monitored on a monthly basis to determine the presence of any specific trends. The recruitment rate (all potential participants), retention and attrition rates (all randomized participants) and completion rates (all enrolled participants) will be assessed at the end of study. Reasons for ineligibility, and/or non-recruitment of eligible patients will be recorded and grouped into categories.
Facilitators and barriers of the interventionDuring the intervention and after 52 week post-TKA follow-upAttendance and exercise logbooks will be used to monitor non-adherence. The instructor will communicate with non-adherent participants to understand the reasons and barriers for non-adherence and to develop appropriate strategies to improve adherence. Furthermore, to assess the acceptability of the intervention, each participant in the intervention group will be invited to participate in a face-to-face or video call interviews semi-structured interview based on participants' preferences within 1 month after the final follow-up.
Sample size estimation for the future definitive trialAfter 52 week post-TKA follow-upBased on the standard deviation (SD) of The Chinese version of the Knee Injury and Osteoarthritis Outcome Scale (the higher the score, the better the performance )so as to inform the sample size calculation for the effectiveness trial.
Self-reported physical function1-week before TKA, 6-, 12-, 24- and 52-week post-TKA follow-upsThe Chinese version of Knee Injury and Osteoarthritis Outcome Scale will be used to document self-reported physical function and to evaluate knee status before/after TKA
Number of trips/falls1-week before TKA, 6-, 12-, 24- and 52-week post-TKA follow-upsThe number of trips, falls and fall-related injuries in the 12 months before baseline will be documented.

Secondary

MeasureTime frameDescription
Global impression of change1-week before TKA, 6-, 12-, 24- and 52-week post-TKA follow-upsSymptom severity, treatment response and the efficacy of treatment 24-weeks post-TKA will be measured by the Global Impression of change scale.
Joint range of motion1-week before TKA, 6-, 12-, 24- and 52-week post-TKA follow-upsThe ranges of motion of hip, knee, and ankle joints will be evaluated using a goniometer. These assessments are chosen because limited knee/ankle joint ranges have been reported as potential risk factors for falls.
Objective measures of static and dynamic stability1-week before TKA, 6-, 12-, 24- and 52-week post-TKA follow-upsWhen wearing the sensors, participants will perform a tandem stance test with eyes open and eyes closed, the TUG and the 6MWT.
Remote monitoring of physical activityover 7 days at 1 week before TKA, 7 days during the 12th , 24th and 52th week afterParticipants' physical activity will be measured by a wearable sensor. accelerometer. The participant will wear ActiGraph on the right hip, near the iliac crest for 7 days except during sleeping, showering or bathing. Data from the vertical axis will be recorded in 15s epochs and be initialized using the normal filter. The data be classified into different activity levels by ActiLife V6.11.0: sedentary (0-99 counts/minute), light (100-2019 counts/minute), moderate (2020-5998 counts/minute), and vigorous (\> 5999 counts/minute).
Balance assessment1-week before TKA, 6-, 12-, 24- and 52-week post-TKA follow-upsThe Brief-Balance Evaluation Systems test comprises six static and six dynamic tasks of different difficulty levels.
Knee pain1-week before TKA, 6-, 12-, 24- and 52-week post-TKA follow-upsIt will be measured by an 11-point numeric pain rating scale, which ranges from 0 (no pain) to 10 (the worst imaginable pain). It documents the current, best, and worst pain in the last 24 hours. It will be used to record the pain intensity of participant's knee and other body parts, if appropriate.
Depression1-week before TKA, 6-, 12-, 24- and 52-week post-TKA follow-upsDepressive symptoms will be examined by the short form Chinese version of the Geriatric Depression Scale, which comprises 15 questions.
Physical activity level1-week before TKA, 6-, 12-, 24- and 52-week post-TKA follow-upsPhysical activity will be assessed by the Physical Activity Scale for the Elderly (Chinese version), which is a 12-item questionnaire that documents leisure, physical, household and work-related activities over the last 7 days.
Fear of falling1-week before TKA, 6-, 12-, 24- and 52-week post-TKA follow-upsConcern of falling will be measured with the Falls Efficacy Scale, which showed good reliability and validity in measuring fear of falling in frail older people.

Countries

Hong Kong

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026