The goal of this study is to to examine the feasibility of a full-scale trial on Helping Hand, a new Joint Protection Program for Hand Osteoarthritis and to examine the acceptability of the new Joint Protection Program. This study will not assess the effectiveness of the program, as it is not designed or powered to do so. Instead, the information gathered will be used to refine the trial design and ensure the future full-scale trial that will assess the effectiveness of the program is robust and successful. The acceptability of the new Joint Protection Program will be assessed through a survey that will be administered to the intervention group at the end of the trial, which will be based on a standardized acceptability framework Participants will: Gain access to an online Joint Protection Program or continue to receive usual care for 12 weeks Visit the clinic or complete online assessments once every 4 weeks Keep a diary of their symptoms and the number of times they used other interventions to manage their symptoms (i.e. painkillers)
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Recruitment Rates
Timeframe: 4, 8, and 12-weeks after randomization
Adherence
Timeframe: 4, 8, and 12-weeks after randomization
Clinical outcome measure completion
Timeframe: baseline, 4, 8, and 12-weeks after randomization
Attrition Rates
Timeframe: 4, 8, and 12-weeks after randomization