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AgingNCT05380180

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

A study testing OneClick Social Engagement Intervention and OneClick Social Engagement Intervention Extension in people with Aging and Mild Cognitive Impairment, run by University of Illinois at Urbana-Champaign at 2 sites in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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… Read more about this study

Who is it for?
Ages 65 years and olderHealthy volunteers can take part
Conditions the study is for
Aging, Mild Cognitive Impairment, Aging Well
What is being tested?
OneClick Social Engagement Intervention and OneClick Social Engagement Intervention Extension
Type of treatment
Pill or oral medicine
Could I receive a placebo?
No, everyone receives an active treatment
How many people
99 participants
Where
2 sitesUnited States
Study dates
15 Apr 2022to 6 Jun 2023
Phase
Interventional
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 65 years and older
  • All sexes
  • Healthy volunteers accepted
  • Older adult

Who may be able to join

  • 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

Who cannot join

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

Trial locations and contacts

2 sites in 1 country.

United States2 sites

  • University of Illinois, Urbana Champaign

    Champaign, Illinois, 61821

  • CJE Senior Living

    Chicago, Illinois, 60645

Other trials in United States

About this study

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.

Being tested
OneClick Social Engagement Intervention, OneClick Social Engagement Intervention Extension
Keywords
videoconferencing, social engagement, loneliness, social isolation, quality of life
Medical subject headings
Cognitive Dysfunction, Social Isolation

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • OneClick Social Engagement InterventionOther

    Intervention group participants 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 will use a computer or tablet to participate in two social engagement events per week. The intervention events will be delivered through the OneClick video conferencing platform. During each session participants will watch a short slideshow around a series of topics (e.g., nature, technology, hobbies) and get to engage in conversations surround the topics presented, which will be held in breakout rooms. Breakout room discussions will be set for 30 minutes, and participants will be provided with questions surrounding the topics to help stimulate conversation.

  • OneClick Social Engagement Intervention ExtensionOther

    Waitlist control group participants will receive no intervention for the first 8 weeks and will complete assessments at week 4 and week 8. Following the completion of the 8-week controlled portion, waitlist participants will be provided with the opportunity to participate in the OneClick social engagement intervention through the intervention extension. Waitlist participants will use a computer or tablet to participate in two social engagement events per week. The intervention events will be delivered through the OneClick video conferencing platform over the span of 8 weeks.

Study groups in NCT05380180
Study groupRoleWhat they receive
OneClick Social Engagement Intervention GroupExperimentalIntervention group participants 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.
Receives: Other: OneClick Social Engagement Intervention
OneClick Social Engagement Waitlist Control GroupOtherWaitlist control group participants will receive no intervention for the first 8 weeks and will complete assessments at week 4 and week 8. Following the completion of the 8-week controlled portion, waitlist participants will be provided with the opportunity to participate in the OneClick social engagement intervention through the intervention extension.
Receives: Other: OneClick Social Engagement Intervention Extension

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in Social Isolation Measured by Friendship Scale

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

    Measured: Baseline, Week 4, Week 8

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

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

    Measured: Baseline, Week 4, Week 8

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

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

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

Secondary outcomes (2)

  1. Change in Social Network Measured by Lubben Social Network Index

    Measures social network size for both family and friends and also the frequency of interaction with them. Higher scores indicate higher level of social engagement. Range (0-30).

    Measured: Baseline, Week 4, Week 8

  2. Change in Social Activity Measured by Social Activity Frequency

    Measures how often during the past year participants have engaged in various social activities. Lower scores indicate less engagement in social activities. Range (10-50).

    Measured: Baseline, Week 4, and Week 8

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 May 2022
  2. Study start15 Apr 2022
  3. Primary completion6 Apr 2023
  4. Study completion6 Jun 2023

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Randomised
Intervention model
Parallel groups
Model description
Participants will be screened and assigned to either intervention group or wait-listed group.
Masking
Single blind
Who is masked
Investigator
Enrolment
99 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05380180
Sponsor's protocol ID
22212
Status last verified
Apr 2026
First submitted
12 May 2022
Last updated
19 May 2026
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Mois G, Lydon EA, Mathias VF, Jones SE, Mudar RA, Rogers WA. Best practices for implementing a technology-based intervention protocol: Participant and researcher considerations. Arch Gerontol Geriatr. 2024 Jul;122:105373. doi: 10.1016/j.archger.2024.105373. Epub 2024 Feb 19.

    PubMed 38460265

  • Lydon EA, Mois G, Shende SA, Myers D, Danilovich MK, Rogers WA, Mudar RA. Methods and baseline characteristics for a social engagement technology-based randomized controlled trial for older adults. Contemp Clin Trials Commun. 2024 May 13;39:101308. doi: 10.1016/j.conctc.2024.101308. eCollection 2024 Jun.

    PubMed 38841566

  • Mois G, Lydon EA, Danilovich MK, Myers D, Chen XS, Mudar RA, Rogers WA. A social engagement technology-based randomized controlled trial for older adults: Outcomes and lessons learned. Contemp Clin Trials Commun. 2025 Jul 28;47:101529. doi: 10.1016/j.conctc.2025.101529. eCollection 2025 Oct.

    PubMed 40822701

Questions about this trial

What is this clinical trial studying?

A study testing OneClick Social Engagement Intervention and OneClick Social Engagement Intervention Extension in people with Aging and Mild Cognitive Impairment, run by University of Illinois at Urbana-Champaign at 2 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 8 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 19 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Yes. Results are posted in the registry (first posted 16 Jan 2026). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in Social Isolation Measured by Friendship Scale (time frame: Baseline, Week 4, Week 8). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05380180, which also lists 3 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 May 2026.

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