Rehabilitation Clinical Trial
Official title:
Mind and Body: A Clinical Trial Evaluation of a Smartphone App-based Mindfulness Intervention to Support Psychosocial Resilience in Aging Patients
This study evaluates the use of a mobile-app delivered mindfulness-based intervention for supporting psychosocial resilience in aging patients undergoing rehabilitation treatment. Half of the patients will receive the mobile-app, while the other half will receive the app 6 months later.
Although, several mobile-app based MBTs are available in the marketplace, there is scant
evidence of high scientific rigor to support their therapeutic efficacy. Furthermore, the
tracking of wellness outcomes, stress resilience and functioning as a result of use of a
therapeutic digital product is a challenging task requiring expertise in technology. In this
study, the investigators aim to investigate not only the effectiveness of an app-based MBT in
aging adults, but also the mechanisms of efficacy - i.e. the therapeutic effects - of app
usage, including changes in, depression, anxiety, or mood and the acceptance of the app in
older adult populations. The investigators also aim to measure the Return On Investment (ROI)
of mobile mindfulness on health services utilization.
The study is a randomized controlled design with 1:1 equal allocation to treatment
(Experimental Am app group) or control (treatment as usual). The investigators will recruit
82 participants in total.
The Experimental group will start the 4 week Am app intervention immediately after
randomization and baseline intervention questionnaires, while the wait-list control group
will receive treatment as usual. Assessments are conducted at four time point: At Baseline
(#1), Post-Intervention (#2), Follow-up at 3 months post baseline (#3) and Follow-up at 6
months post baseline (#4).
The clinical champions that referred the patient to the study will complete brief surveys
about the quality of their appointments with the patient at two time points: At baseline (#1)
and Post-Intervention (#2).
The waitlist control group will be granted access to the mindfulness intervention at 6 months
post baseline.
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