To goal of this study is to pilot the SickleFit exercise and nutrition intervention in adults with sickle cell disease in a randomized control trial
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Feasibility of Randomization
Timeframe: From enrollment to the last paticipants randomized over a 2 year period
Safety/Adverse Events
Timeframe: adverse events will be measured for both arms up to 6 months
Acceptability
Timeframe: From enrollment to after completion of the SickleFit Program over 6 months since we will also measure acceptability for control group
Retention in the program
Timeframe: From the baseline Sickle Cell Disease Functional Assessment to the post-SCD-FA. Over a 30 week period since post assessments will be completed within 3 months of completion of the SickleFit program or control period.
Adherence
Timeframe: From the start of the first SickleFit session to the end of the SickleFit program at 12 weeks