Mobile Health App Program to Reduce Physical and Psychological Stress After the COVID-19 Pandemic for Adults Aged 18 to 70
Led by The Hong Kong Polytechnic University · Updated on 2024-02-28
814
Participants Needed
1
Research Sites
78 weeks
Total Duration
AI-Summary
What this Trial Is About
Researchers are studying the impacts of physiological and psychological distress related to COVID-19 and its aftermath, including long-term effects such as depression, anxiety, fatigue, sleep problems, and pain. This trial evaluates a mobile health app called Health Apps for Post-Pandemic Years HAPPY, designed using the Transactional Model of Stress and Coping Theory, to help people manage these distress symptoms during the post-pandemic era. The study involves both individuals affected by COVID-19 and those experiencing related distress without having had COVID-19.
The trial includes two groups an experimental group receiving a 24-week intervention with three levels of support, and a waitlist control group. The intervention provides tailored coping strategies based on participants distress assessments, including physical activity training with motion sensors and wearable devices, mindfulness-based sessions delivered via animation videos, and energy conservation techniques. The experimental group receives 8 weeks of supervised sessions followed by 16 weeks of self-help practice, while the control group receives health promotion materials initially and access to the intervention after 24 weeks.
Participants will wear commercial wearable sensors to track physical activity and sync data with the app. Researchers will measure changes in psychological distress, fatigue, sleep quality, pain, emotional regulation, self-efficacy, and stress symptoms at baseline and after 24 weeks. The study monitors participants progress and coping abilities throughout the intervention and follow-up, aiming to assess the apps effects on managing post-pandemic distress over time.
CONDITIONS
Brief Title
A Health Apps for Post-Pandemic Years for People With Physiological and Psychosocial Distress
Research Team
J
Justina Liu, PhD
A
Amy Cheung, MA
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Exhibiting physiological and/or psychosocial distress as indicated by specific scores on the Kessler Psychological Distress Scale, Brief Fatigue Inventory, Pittsburgh Sleep Quality Index, or Numerical Pain Scale
Has access to the Internet and a smartphone
You will not qualify if you...
Individuals with severe cognitive impairments
Individuals with severe visual impairments
Individuals with severe hearing impairments
Any health conditions that could prevent participation in the HAPPY program
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Treatment
Duration - 24 weeks
Participants in the experimental group receive an 8-week intervention with weekly supervised sessions that include physical activity training, mindfulness-based intervention, and energy conservation techniques tailored to their distress symptoms. This is followed by a 16-week self-help phase where participants continue practicing these interventions at home, supported by a Health Apps program designed to improve coping and reduce distress.
Weekly visits for the first 8 weeks (supervised sessions), then self-practice at home for 16 weeks
Follow-up
Duration - Duration of follow-up not specifically defined beyond 24 weeks
Participants are monitored to assess the mid-term effects of the intervention on physiological and psychosocial distress after completing the 24-week program.
Visits aligned with outcome assessments at 24 weeks
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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Published Research Related To This Trial
The prevalence of depressive and anxiety symptoms and their associations with quality of life among clinically stable older patients with psychiatric disorders during the COVID-19 pandemic.
A Health App for Post-Pandemic Years (HAPPY) for people with physiological and psychosocial distress during the post-pandemic era: Protocol for a randomized controlled trial.
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