Collaborative Care With Smart Health Management Program for Patients With Chronic Illness

Sponsor
Seoul National University Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT03294057
Collaborator
Korea Health Industry Development Institute (Other), National Evidence-Based Healthcare Collaborating Agency (Other), National Institute of Health, Korea (Other), National Clinical Research Coordination Center, Seoul, Korea (Other), Seoul National University Bundang Hospital (Other)
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Study Details

Study Description

Brief Summary

This study verifies efficacy of collaborative care with Smart Health Management Program developed for patients with chronic illness. The aim of the study is to observe the changes in clinical indicators, quality of life and health related behaviors when providing self-management programs with ICT for chronic disease patients.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Tele-coaching programs
  • Behavioral: ICT programs
  • Behavioral: A book about chronic disease
N/A

Detailed Description

This study is to demonstrate that chronic disease patients receiving collaborative care with ICT-based self-management and educational program can improve clinical outcomes and overall health status, including quality of life and health habits.

In addition to the economic burden, people with chronic disease experience various psychosocial crises such as anxiety and depression, which causes the deterioration of overall quality of life and increases social burden. The collaborative care management based Chronic Care Model (CCM) have provided coaching by a medically supervised nurse, working with each patient's physician. However, standard CCM have limitations in that they do not provide self-management strategies of the patient in detail. Therefore, to improve the effectiveness of the CCM model, it is required to propose a new approach to the utilization of IT-based self-management program that is currently being developed to increase accessibility and efficiency of health care service.

Primary outcomes of this study are as follow: Improvement of depression in patients with osteoporosis, chronic respiratory disease and chronic arthritis.

Participants in this study will respond a baseline questionnaire about depressive mood, health habits, health behavior patterns and quality of life, diet, exercise, etc. After that, participants will be allocated equally into three groups - the intervention group 1, intervention group 2 and the control group. The intervention group 1 will receive S Healthing and a tele- coaching program conducted 12 times (one time for one week), and more than 20 minutes each by a trained nurse. The intervention group 2 will receive S Healthing while the control group will receive basic educational material on the disease. Coaching content consists specifically of: 1) evaluation, 2) facing and accepting the health crisis, 3) setting up new goals, 4) making decisions and plans, and 5) practice. "S Healthing" is based ICT- program and includes educational contents and self-management program based on Smart Management Strategy for Health (SMASH). The intervention group 1, 2 will conduct self-management for 3 months through smart phone application and web program. Participants will receive a questionnaire about the quality of life and health habits with the clinical examination 3 months after baseline survey was conducted. The result from two questionnaires (baseline, 3 months post-intervention) and clinical outcome of baseline and 3 months will be compiled and be compared with others.

Study Design

Study Type:
Interventional
Actual Enrollment :
54 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Parallel AssignmentParallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
The Effectiveness of Collaborative Care With Smart Health Management Program for Patients With Chronic Illness: Randomized Controlled Trial
Actual Study Start Date :
Oct 27, 2017
Actual Primary Completion Date :
Jun 7, 2018
Actual Study Completion Date :
Jun 30, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: ICT programs + Tele-coaching programs

ICT programs that include health information learning by disease and self-management based on Smart Management Strategy for Health (SMASH) are provided. And a trained nurse provides tele-coaching programs to subjects. After that, subjects will conduct self-management health care and tele-coaching programs for 12 weeks. After 3 months, they finish self-management ICT + coaching programs, and then they fill out the questionnaire.

Behavioral: Tele-coaching programs
Tele-coaching program conducted 12 times (one time for one week), and more than 20 minutes each by a trained nurse. Coaching content specifically, 1) evaluation, 2) facing and accepting the health crisis, 3) setting up new goals, 4) making decisions and plans, and 5) practice.

Behavioral: ICT programs
ICT programs that include health information learning by disease and self-management based on Smart Management Strategy for Health (SMASH)

Experimental: ICT programs

ICT programs that include health information learning by disease and self-management based on Smart Management Strategy for Health (SMASH) are provided. After that, subjects will conduct self-management health care for 12 weeks. After 3 months, they finish self-management ICT programs, and then they fill out the questionnaire.

Behavioral: ICT programs
ICT programs that include health information learning by disease and self-management based on Smart Management Strategy for Health (SMASH)

Active Comparator: A book about chronic disease

Subjects in the group get a book about chronic disease for patients. After 3 months, they finish reading the materials, they fill out the questionnaire.

Behavioral: A book about chronic disease
A Take-home book about chronic disease are provided for self-education

Outcome Measures

Primary Outcome Measures

  1. Depression [Baseline, 3 months post-intervention]

    Improvement of depression (PHQ-9)

Secondary Outcome Measures

  1. Health behavior patterns [Baseline, 3 months post-intervention]

    We identify health habits by dividing into five steps according to the TTM stage. We evaluate Increase in maintenance rate of health behavior patterns.

  2. Health Management Strategies [Baseline, 3 months post-intervention]

    Improvement of Health Management Strategies by SAT (We use Smart Management Strategy for Health Assessment Tool (SAT) to assess their self-management (SM) strategies of health by themselves).

  3. Quality of life (Mcgill QoL) [Baseline, 3 months post-intervention]

    Improvement of quality of life (Mcgill QoL)

  4. Quality of life (EuroQoL) [Baseline, 3 months post-intervention]

    Improvement of quality of life (EuroQoL)

  5. Quality of life (SF-12) [Baseline, 3 months post-intervention]

    Improvement of quality of life (SF-12)

  6. Physical activity [Baseline, 3 months post-intervention]

    Changes in exercise (Godin's Leisure Time Exercise Questionnaire)

Eligibility Criteria

Criteria

Ages Eligible for Study:
19 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Subject 19 years old and more

  • Subject who understands the purpose of the study and signs with informed consent form

  • Subject with chronic disease (osteoporosis, chronic pulmonary disease, chronic arthritis)

  • Subject with METs less than 12.5 hours per week

  • Subjects who use smart phones and PCs (those who can use ICT-based health care programs)

Exclusion Criteria:
  • Inability to speak, understand, or write Korean

  • Inability to understand the contents of the provided materials due to poor eyesight and hearing

  • Medical conditions that would limit adherence to participation of the clinical trial (as confirmed by their referring physician; e.g. dyspnea, severe depression and other mental disorders)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Seoul National University Hospital Seoul Korea, Republic of 03080

Sponsors and Collaborators

  • Seoul National University Hospital
  • Korea Health Industry Development Institute
  • National Evidence-Based Healthcare Collaborating Agency
  • National Institute of Health, Korea
  • National Clinical Research Coordination Center, Seoul, Korea
  • Seoul National University Bundang Hospital

Investigators

  • Principal Investigator: Young Ho Yun, MD, PhD, Seoul National University Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Young Ho Yun, Principal Investigator, Seoul National University Hospital
ClinicalTrials.gov Identifier:
NCT03294057
Other Study ID Numbers:
  • HI16C0455-2
First Posted:
Sep 26, 2017
Last Update Posted:
Mar 17, 2021
Last Verified:
Mar 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Young Ho Yun, Principal Investigator, Seoul National University Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 17, 2021