Habitual Physical Activity and Sedentary Behavior Following Total Knee Arthroplasty

Knee Osteoarthritis Clinical Trial

Official title:

The Effect of Total Knee Arthroplasty on Habitual Physical Activity, Sedentary Behaviour and Health Outcomes in Patients With Osteoarthritis

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02675062
• Other study ID #: M150323
• Status: Completed
• Phase: N/A
• First received: January 29, 2016
• Last updated: May 1, 2017
• Start date: August 2015
• Est. completion date: April 30, 2017

Study information

• Verified date: May 2017
• Source: University of Witwatersrand, South Africa
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The purpose of this study is to determine whether habitual physical activity and sedentary behaviour improve six weeks and between three to six months after total knee replacement surgery in people with osteoarthritis.

Description:

The aims of this study are to

1. describe habitual physical activity and sedentary behaviour patterns in knee osteoarthritis patients who are scheduled for total knee arthroplasty,

2. investigate the effects of unilateral primary total knee arthroplasty on objectively and subjectively measured physical activity, sedentary behaviour and health outcomes of knee OA patients and

3. compare subjective measures of functional ability and sedentary behaviour (questionnaires) with objective measures of habitual physical activity and sedentary behaviour (accelerometry) both before and after total knee arthroplasty.

Study design:

This a longitudinal follow-up study of a cohort of participants who have been diagnosed with knee osteoarthritis and who will all be undergoing total knee arthroplasty. After enrolment into the study, baseline assessments will be done prior to total knee arthroplasty. After total knee arthroplasty, participants will be followed-up and the same assessments done at baseline will also be done at 6 weeks, and 3 to 6 months post-operatively. Habitual physical activity and sedentary behaviour will be measured using accelerometry (Actigraph GTX3+ and ActivPal monitors) at the specific time points.The ActiGraph will be worn by participants for 24 hours/day for seven days at each of the assessment time points. It will be attached to an elastic nylon strap which the participants can wear as a belt around the waist on the side of right/left hip (depending on which knee is being operated on). Thus, the ActiGraph will be worn on the side of left hip if the total knee arthroplasty is on the left knee and vice versa. Participants will be asked to remove the ActiGraph when showering, bathing or swimming. After seven days of accelerometer wear, the accelerometers will be collected at the next possible visit to the hospital or arrangement will be made for collection from participants at a location most convenient to them. An ActivPAL will be taped to the thigh of the patient with waterproof taping and the patient will be asked to keep the ActivPAL on for the same amount of time as the ActiGraph. The ActivPAL can be covered with waterproof taping therefore, there will be no need to remove the ActivPAL when showering, bathing or swimming. The ActivPAL will be collected at the same time as the ActiGraph. In addition, general health, functional ability, generic quality of life and sleep and pain questionnaires will be conducted at each time point on each participant.

Study Site:

The study will be conducted at the Charlotte Maxeke Academic Hospital in Johannesburg, South Africa. It is an accredited central hospital with about 1088 beds serving patients from across Gauteng and neighbouring provinces. The hospital is situated in Parktown and also, serves as the main teaching hospital for the University of the Witwatersrand, Faculty of Health Sciences. Study participants will be recruited from the Division of Orthopaedics in the hospital. This hospital is chosen because: (1) it is a tertiary hospital that runs several specialist clinics including the Orthopaedic Division where total knee arthroplasty is performed and (2) there is a collaboration between the Academic staff of the Faculty of Health Sciences of University of the Witwatersrand and the hospital Staff for teaching and research which will facilitate accessibility to patients.

Sample Size Determination:

Based on an anticipated 2% decrease in the amount of time spent in sedentary behaviour per day (which, for an average 16 hour day, equates to a 20 minute reduction), a sample size calculation shows that a total sample of 107 participants will be required in this study to detect a significant effect of knee arthroplasty on sedentary behaviour with a power of 80%.

The effect of the total knee arthroplasty on the change in habitual physical activity and sedentary behaviour will be assessed between the three timepoints (baseline, six weeks and three to six months).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 80
• Est. completion date: April 30, 2017
• Est. primary completion date: April 30, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 55 Years to 80 Years

Eligibility

Inclusion Criteria:

• clinical diagnosis of knee osteoarthritis

• Kellgren and Lawrence grade 4 severity of knee osteoarthritis

• refractory to analgesics for at least six months

• undergoing primary or first-time single total knee arthroplasty

• are ambulant with or without assistive devices

Exclusion Criteria:

• use assistive ambulatory devices for mobility problems other than knee osteoarthritis

• scheduled for bilateral knee arthroplasty, a second knee arthroplasty or revision

• scheduled for total hip replacement

• co-morbidities or medical conditions that affect physical activity such as congestive heart failure, stroke and other neurological problems, chronic obstructive pulmonary disease, gout and/or sepsis

• rheumatoid arthritis

• undergoing another surgery following the knee arthroplasty

• non-ambulant or wheel chair-bound

Related Conditions & MeSH terms

• Knee Osteoarthritis
• Osteoarthritis
• Osteoarthritis, Knee

Locations

Country	Name	City	State
South Africa	Division of Orthopaedics, Charlotte Maxeke Johannesburg Academic Hospital	Johannesburg	Gauteng

Sponsors (1)

Lead Sponsor	Collaborator
University of Witwatersrand, South Africa

Country where clinical trial is conducted

South Africa, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Habitual physical activity level	Measured using the ActiGraph accelerometer	Baseline
Primary	Habitual physical activity level	Measured using the ActiGraph accelerometer	Six weeks post-op
Primary	Habitual physical activity level	Measured using the ActiGraph accelerometer	Between three and six months post-op
Primary	Time spent in sedentary behaviour	Measured using the activPAL accelerometer	Baseline
Primary	Time spent in sedentary behaviour	Measured using the activPAL accelerometer	Six weeks post-op
Primary	Time spent in sedentary behaviour	Measured using the activPAL accelerometer	Between three and six months post-op
Secondary	Knee osteoarthritis-specific quality of life	Measured using Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)	Baseline, 6 weeks post-op, between 3 and 6 months post-op
Secondary	Activity	Measured using the UCLA activity index (self-report)	Baseline, 6 weeks post-op, between 3 and 6 months post-op
Secondary	Pain	Measured using a visual analogue scale	Baseline, 6 weeks post-op, between 3 and 6 months post-op
Secondary	Sleep quality	Measured using a sleep questionnaire	Baseline, 6 weeks post-op, between 3 and 6 months post-op
Secondary	Total summed score of pain, activity, sport and recreation function and knee-related quality of life.	Measured using the Knee injury and Osteoarthritis Outcome Score (KOOS)	Baseline, 6 weeks post-op, between 3 and 6 months post-op
Secondary	Score of pain and physical disability	Measured using the Oxford Knee Score (OKS)	Baseline, 6 weeks post-op, between 3 and 6 months post-op
Secondary	Knee functional score	Measured using the Knee Society Clinical Rating System (KSS)	Baseline, 6 weeks post-op, between 3 and 6 months post-op
Secondary	Patient functional score	Measured using the Knee Society Clinical Rating System (KSS)	Baseline, 6 weeks post-op, between 3 and 6 months post-op