Digital Motivation to Decrease Inactive Behaviour in Patients With Knee Osteoarthritis
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|ClinicalTrials.gov Identifier: NCT03339011|
Recruitment Status : Active, not recruiting
First Posted : November 9, 2017
Last Update Posted : June 18, 2018
Physical inactivity is a major risk behaviour with a potential for causing premature death, particularly among people with mobility limitations, such as knee osteoarthritis.
Digital motivational interventions (such as SMS) can motive to a healthy behaviour including increased physical activity.
The purpose of this study is to investigate if motivational text messages following an exercise intervention to improve mobility limitations will change the physical activity level in patients with knee osteoarthritis.
This study is designed as pilot randomized controlled trial, with equal randomization (1:1). Eligible participants will be randomised into one of two groups (intervention or control) after completing their baseline measurements. The intervention group will receive weekly motivational text messages and the control group will not receive any attention from the study.
|Condition or disease||Intervention/treatment||Phase|
|Knee Osteoarthritis||Behavioral: Motivational SMS text message||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||38 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Single (Outcomes Assessor)|
|Primary Purpose:||Supportive Care|
|Official Title:||Effectiveness of Text Messages for Decreasing Inactive Behavior in Patients With Knee Osteoarthritis: a Pilot Randomised Controlled Study|
|Actual Study Start Date :||November 14, 2017|
|Estimated Primary Completion Date :||July 13, 2018|
|Estimated Study Completion Date :||November 14, 2018|
Experimental: SMS text message
The content of the text messages is developed based on recommendation and advice from the Danish Health Authority about the importance of regular daily physical activity.
For 6 weeks, the text messages will be send three times per week, twice during the week days and once in the weekend, based on previous experience with SMS as motivation for chronic pain patients.
Behavioral: Motivational SMS text message
Motivational text messages delivered to the participants' mobile phones. The text messages contain motivational text and advice on physical activity.
No Intervention: No intervention
No attention from the study
- Change from baseline in physical inactivity [ Time Frame: 6 weeks ]Physical inactivity is measured using an accelerometer based activity monitor. Physical activity is defined as time (in minutes) spent inactive, i.e. lying, sitting, standing during a day.
- Change form baseline in the Knee Injury and Osteoarthritis Outcome Score (KOOS) [ Time Frame: 6 weeks ]The Knee injury and Osteoarthritis Outcome Score (KOOS) questionnaire is used to assess patient reported outcomes on pain, function, and quality of life.
- Transition questionnaire (TRANS-Q) of perceived change in knee symptoms [ Time Frame: 6 weeks ]To investigate if participants experience a change in their osteoarthritis symptoms over time, they will be asked: "Pleas answer if you feel that your osteoarthritis symptoms have change for either the better, worse or no changes compared to before you entered this study" at the follow-up visit. The Participants can then check a box say: not change, a change for the worse or change for the better
- Self-reported change in physical inactivity [ Time Frame: 6 weeks ]At the follow-up visit participants will be asked "Have you changed your physical activity behaviour after completing the motivational intervention". This question will be asked at the end of the intervention period to investigate if the objective measurement of sedentary behaviour is related to the participants own perceived behaviour.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03339011
|The Parker Institute, Bispebjerg and Frederiksberg University Hospitals|
|Copenhagen, Denmark, 2000|