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Effectiveness of a Culturally Adapted Online Education Program (iSupport-Korea) for Family Caregivers of People With Dementia: A Randomized Controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This randomized controlled trial evaluates the effectiveness of iSupport-Korea, a culturally adapted online education program for family caregivers of people with dementia. A total of 160 caregivers will be randomly assigned to either the intervention or control group and followed for 4 months. The investigators hypothesize that the intervention group will show greater improvements in care-related quality of life, caregiver self-efficacy, and family decision-making self-efficacy.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 19
Healthy Volunteers: f
View:

• Adults aged 19 years or older

• Family caregivers currently providing care for a person diagnosed with dementia

• Informal caregivers such as spouse, children, or relatives

• Living with the person with dementia or providing regular care even if not cohabiting

• Able to read and understand Korean and communicate in Korean

• Able to use digital devices (e.g., smartphone, tablet, or computer) to access an online program

• Willing to provide informed consent and participate in the study

Locations
Other Locations
Republic of Korea
College of Nursing, Chungnam National University
RECRUITING
Daejeon
Contact Information
Primary
JINSOL SON
jinsoleei21@gmail.com
+8242-580-8407
Time Frame
Start Date: 2026-05-13
Estimated Completion Date: 2027-04-04
Participants
Target number of participants: 160
Treatments
Experimental: iSupport-Korea Group
Participants will receive access to the iSupport-Korea program for 2 months.
Active_comparator: Dementia Information Website Group
Participants will be provided access to publicly available dementia-related informational websites, such as those provided by dementia care centers.
Related Therapeutic Areas
Sponsors
Leads: Chungnam National University

This content was sourced from clinicaltrials.gov