Actively Recruiting

Phase Not Applicable
Age: 18Years - 70Years
All Genders
ID05459896

A Health Apps for Post-Pandemic Years (HAPPY) for People With Physiological and Psychosocial Distress During the Post-Pandemic Era

Led by The Hong Kong Polytechnic University · Updated on 2024-02-28

814

Participants Needed

1

Research Sites

78 weeks

Total Duration

On this page

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 app's 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

Who Can Participate

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 18 and older
  • 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
Not Eligible

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

AI-Screening

AI-Powered Screening

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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

Trial Site Locations

Total: 1 location

1

The Hong Kong Polytechnic University

Hong Kong, Hong Kong

Actively Recruiting

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Research Team

J

Justina Liu, PhD

A

Amy Cheung, MA

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

Mental health interventions and supports during COVID- 19 and other medical pandemics: A rapid systematic review of the evidence.

Sophie Soklaridis, Elizabeth Lin, Yasmin Lalani...

https://pubmed.ncbi.nlm.nih.gov/32858431

Evidence Synthesis of Digital Interventions to Mitigate the Negative Impact of the COVID-19 Pandemic on Public Mental Health: Rapid Meta-review.

Christian Rauschenberg, Anita Schick, Dusan Hirjak...

https://pubmed.ncbi.nlm.nih.gov/33606657

Association Between Depression, Health Beliefs, and Face Mask Use During the COVID-19 Pandemic.

Daniel Thomas Bressington, Teris Cheuk Chi Cheung, Simon Ching Lam...

https://pubmed.ncbi.nlm.nih.gov/33192697

Effects of an mHealth Brisk Walking Intervention on Increasing Physical Activity in Older People With Cognitive Frailty: Pilot Randomized Controlled Trial.

Rick Yc Kwan, Deborah Lee, Paul H Lee...

https://pubmed.ncbi.nlm.nih.gov/32735218

Perceived Risk and Protection From Infection and Depressive Symptoms Among Healthcare Workers in Mainland China and Hong Kong During COVID-19.

Simon Ching Lam, Teresa Arora, Ian Grey...

https://pubmed.ncbi.nlm.nih.gov/32765321

Effective behavioral intervention strategies using mobile health applications for chronic disease management: a systematic review.

Jung-Ah Lee, Mona Choi, Sang A Lee...

https://pubmed.ncbi.nlm.nih.gov/29458358

Face Mask Wearing Behaviors, Depressive Symptoms, and Health Beliefs Among Older People During the COVID-19 Pandemic.

Rick Yiu Cho Kwan, Paul Hong Lee, Daphne Sze Ki Cheung...

https://pubmed.ncbi.nlm.nih.gov/33614680