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The Application of Wearable Technology to Improve the Physical Activity Level of People With Chronic Mental Illness

NCT03408327 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2020-11-06

No results posted yet for this study

Summary

The object is to develop a physical activity promotion program by applying social cognitive theory and wearable technology and evaluate its feasibility in people with MI

Stage I: Accuracy, Acceptability, Feasibility. Stage II: Effectiveness Analysis

In stage II, will conduct a single-blinded, randomized controlled study. 90 participants will be randomly assigned to experimental group or control group. The intervention for both groups will last for 12 weeks, with a 12-week of follow-up. The measurements include physical activity level, physical fitness, cognitive function and sleep quality, as well as the moderators of the effectiveness of program.

Conditions

  • Schizophrenia
  • Physical Activity
  • Health Knowledge, Attitudes, Practice

Interventions

DEVICE

Wearable technology

Fitness wristband \& APP

BEHAVIORAL

LINE group

Promote social interaction

BEHAVIORAL

Group activities

Which was developed by applying social cognitive theory

DEVICE

Health promotion manual

Which was about general physical activity promotion content

Sponsors & Collaborators

  • Kaohsiung Medical University Chung-Ho Memorial Hospital

    lead OTHER

Principal Investigators

  • Ming-De Chen, Ph.D. · Department of Occupational Therapy, Kaohsiung Medical University

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
64 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-03-16
Primary Completion
2020-07-31
Completion
2020-07-31

Countries

  • Taiwan

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03408327 on ClinicalTrials.gov