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N/A N=99 Randomized Single-blind Other

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

Aging · Mild Cognitive Impairment · Aging Well

Enrolled (actual)
99
Serious AEs
0.0%
Results posted
Jan 2026
Primary outcome: Primary: Change in Social Isolation Measured by Friendship Scale — 20.37; 20.54; 20.05; 20.23 score on a scale — p=<.05

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
OneClick Social Engagement Intervention (Other); OneClick Social Engagement Intervention Extension (Other)
Age
Older Adult · 65+ yrs
Sex
All
Sponsor
University of Illinois at Urbana-Champaign
Primary completion
Apr 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
Change in Social Isolation Measured by Friendship Scale
20.37; 20.54; 20.05; 20.23; 20.39; 19.54 <.05 sig
PRIMARY
Change in Loneliness Measured by University of California - Los Angeles (UCLA) Loneliness Scale
37.93; 37.08; 40.34; 38.60; 38.05; 39.00 <.05 sig
PRIMARY
Change in Quality of Life Measured by Quality of Life in Alzheimer's Disease
37.52; 37.81; 36.88; 36.63; 37.44; 36.54 <.05 sig
SECONDARY
Change in Social Network Measured by Lubben Social Network Index
18.75; 19.08; 17.59; 17.28; 17.51; 17.54 <.05 sig
SECONDARY
Change in Social Activity Measured by Social Activity Frequency
26.84; 27.98; 27.63; 27.89; 28.07; 27.30 <.05 sig

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.

Eligibility Criteria

Inclusion Criteria

  • Age 65+
  • 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
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05380180). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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