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Clinical Trials/NCT06785857
NCT06785857CompletedNot Applicable

An Intervention Effect Study of a Mobile Medical Supportive Care Program for Family Caregivers With Dementia Combined With Diabetes: a Randomized Controlled Trial

Yuanjiao Yan1 site in 1 country60 target enrollmentStarted: May 1, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
60
Locations
1
Primary Endpoint
Caregiver Burden Inventory- Baseline (Month 0)

Study Overview

Brief Summary

The purpose of this project is to evaluate the effectiveness of the clinical application of a mHealth supportive care program for family caregivers with dementia combined with diabetes based on the supportive care framework. The results of the study will provide family caregivers with more economical and efficient care guidance, thereby improving the quality of care and quality of life for people with dementia and diabetes in general.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
Single (Outcomes Assessor)

Masking Description

The intervention group received an mHealth supportive care program, the control group received an offline supportive care program, and all caregivers received health education related to diabetes and dementia. The intervention was conducted concurrently in the experimental and control groups, and both groups were followed up in the home once a month for 12 weeks, with each caregiver receiving three 1-hour visits from the researcher.

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Caregivers:
  • •caregivers and patients have legal kinship (such as spouses, children or siblings) and other non-costly caregivers such as babysitters, bellhops, etc.;
  • •caregiving work ≥ 8 hours / day, care for the patient ≥ 5 days a week, the care time ≥ 1 month;
  • •conscious adults with a certain degree of reading and comprehension;
  • •at least have a smart phone (with Internet access) and will be able to use it proficiently;
  • •informed consent and voluntary participation in the study. Informed consent and voluntary participation in the study.
  • •meet the diagnostic criteria of Alzheimer's disease;
  • •meet the diagnostic criteria of type 2 diabetes mellitus;
  • •age ≥ 60 years old, permanent residents of the district.

Exclusion Criteria

  • •Caregivers:
  • •severe physical or mental illness;
  • •people with drug or alcohol dependence;
  • •caregivers who are participating in a similar intervention study.
  • •Caregivers:
  • •patients with severe physical illnesses, major illnesses, or terminal illnesses;
  • •patients with drug or alcohol dependence.

Arms & Interventions

an offline supportive care program

Active Comparator

This was done routinely in accordance with the requirements of public health services for chronic diseases in the community elderly. In addition, health education on diabetes mellitus and dementia was provided to the caregivers during their monthly home visits.

① the content of diabetes health education: the researcher gave the caregivers education and training on the care of diabetes patients: the main points of care in diet, sleep, exercise, etc.

② The content of dementia health education: the researcher gave the caregivers education and training related to the care of dementia patients: instructing the caregivers in the basic life care skills of patients' diet, sleep, exercise, etc.

Intervention: Offline supportive care (Other)

mHealth Supportive Care Program

Experimental

On the basis of the monthly home visits in the control group, "Xiamen iHealth" was used as a medium to add a weekly mHealth supportive care intervention program, with one supportive care item every two weeks for 12 weeks, for a total of 12 online interventions, as well as to provide online consultation and appointment services for caregivers at any time.

Intervention: mHealth Supportive Care Program (Other)

Outcomes

Primary Outcomes

Caregiver Burden Inventory- Baseline (Month 0)

Time Frame: Baseline (pre-intervention)

The scale used in this study was obtained by Rui Zhang based on the Chinese version of the CBI by Taiwanese scholar Guiru Zhou, who modified the questionnaire according to the linguistic characteristics of mainland China.The CBI was initially used to measure the evaluation of the burden on caregivers of patients with dementia, which includes multiple dimensions such as physical burden, emotional burden, social burden, time-dependent burden, and developmentally limited burden, and the scoring of each entry was based on a Likert 5-point scale ranging from strongly agree (4) to strongly disagree (0). Likert 5-point scale from strongly agree (4 points) to strongly disagree (0 points). Total scale scores ranged from 0 to 96; higher scores indicated greater caregiver burden. When the score is ≥ 24, consideration should be given to receiving therapeutic interventions; when the score is greater than or equal to 36, it suggests the risk of severe burden.

Caregiver Burden Inventory - Post-intervention (Month 3)

Time Frame: Post-intervention (Month 3)

The scale used in this study was obtained by Rui Zhang based on the Chinese version of the CBI by Taiwanese scholar Guiru Zhou, who modified the questionnaire according to the linguistic characteristics of mainland China.The CBI was initially used to measure the evaluation of the burden on caregivers of patients with dementia, which includes multiple dimensions such as physical burden, emotional burden, social burden, time-dependent burden, and developmentally limited burden, and the scoring of each entry was based on a Likert 5-point scale ranging from strongly agree (4) to strongly disagree (0). Likert 5-point scale from strongly agree (4 points) to strongly disagree (0 points). Total scale scores ranged from 0 to 96; higher scores indicated greater caregiver burden. When the score is ≥ 24, consideration should be given to receiving therapeutic interventions; when the score is greater than or equal to 36, it suggests the risk of severe burden.

Secondary Outcomes

  • Social Support Rating Scale - Post-intervention (Month 3)(Post-intervention (Month 3))
  • Dementia Caring Knowledge Scale - Post-intervention (Month 3)(Post-intervention (Month 3))
  • Social Support Rating Scale - Baseline (Month 0)(Baseline (Pre-intervention))
  • Dementia Caring Knowledge Scale-Baseline (Month 0)(Baseline (Pre-intervention))

Investigators

Sponsor
Yuanjiao Yan
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Yuanjiao Yan

Sponsor-Investigator

Fujian Provincial Hospital

Study Sites (1)

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