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Clinical Trials/NCT05380180
NCT05380180
Completed
N/A

Enhancing Quality of Life for Older Adults With and Without Mild Cognitive Impairment (MCI) Through Social Engagement Over Video Technology

University of Illinois at Urbana-Champaign2 sites in 1 country99 target enrollmentApril 15, 2022

Overview

Phase
N/A
Intervention
Not specified
Conditions
Aging
Sponsor
University of Illinois at Urbana-Champaign
Enrollment
99
Locations
2
Primary Endpoint
Change in Social Isolation Measured by Friendship Scale
Status
Completed
Last Updated
3 months ago

Overview

Brief Summary

The goal of this randomized controlled trial is to rigorously assess the efficacy of an 8-week social engagement OneClick intervention. A total of 120 older adults with and without mild cognitive impairment (60 per group) will be randomized after a baseline assessment to the social engagement OneClick intervention group or the waitlist control group. Participants assigned to the intervention group will receive the social engagement OneClick intervention for 8 weeks, and will complete a mid-assessment at week 4, and a post-assessment at week 8. Participants assigned to the waitlist control group will receive no intervention for the first 8 weeks and will complete assessments at week 4 and week 8. Subsequently, as an extension to this study, participants assigned to the waitlist control group will have an opportunity to participate in 8 weeks of social engagement OneClick intervention.

Registry
clinicaltrials.gov
Start Date
April 15, 2022
End Date
June 6, 2023
Last Updated
3 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Wendy Rogers

Khan Professor of Applied Health Sciences

University of Illinois at Urbana-Champaign

Eligibility Criteria

Inclusion Criteria

  • Fluent in English
  • Adequate visual and auditory acuity
  • Passing score on Telephone Interview for Cognitive Status - Modified (TICS-M) of 22 and above included
  • Passing score on Montreal Cognitive Assessment (MoCA) of 20 and above included
  • Geriatric Depression Scale (GDS) score of less than 9
  • Stated willingness to comply with all study procedures and availability for the duration of the study
  • Access to and ability to use necessary resources for participating in technology-based intervention

Exclusion Criteria

  • Diagnosis of dementia
  • Live in assisted living facility or skilled nursing facility

Outcomes

Primary Outcomes

Change in Social Isolation Measured by Friendship Scale

Time Frame: Baseline, Week 4, Week 8

Measures six dimensions that contribute to social isolation. Lower scores indicate lower extent of social isolation. Range (0-24)

Change in Loneliness Measured by University of California - Los Angeles (UCLA) Loneliness Scale

Time Frame: Baseline, Week 4, Week 8

Measures the respondents' subjective feeling of loneliness. Higher scores indicate a greater feeling of loneliness. Range (20-80).

Change in Quality of Life Measured by Quality of Life in Alzheimer's Disease

Time Frame: Time Frame: Baseline, Week 4, Week 8

Measures quality of life indicators such as physical health, energy, family, and money. Lower scores indicate a lower quality of life. Range (13-52).

Secondary Outcomes

  • Change in Social Network Measured by Lubben Social Network Index(Baseline, Week 4, Week 8)
  • Change in Social Activity Measured by Social Activity Frequency(Baseline, Week 4, and Week 8)

Study Sites (2)

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