ClinicalTrials.gg
Not yet recruitingNCT07881510Updated Oct 22, 2026

Artificial Intelligence and Digital Health Literacies Among Older Adults: A Mixed-method Pilot Intervention Study

An interventional study of AI and digital health literacy program (E2NGAGE-Literacy) in Digital Health Literacy, AI Chatbot and Aged 60 Years or Older, sponsored by National University of Singapore. Not yet recruiting. Open to participants aged 60 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-22.

Sponsored by National University of Singapore · Not applicable, Interventional, and Other

Updated Oct 19, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
60 Years and older
Sex
All
01

Study summary

The goal of this pilot study is to determine the feasibility and to learn if a training program called E2NGAGE-Literacy (Empowering Elders in Navigating Generative AI for Greater E-health Literacy) can potentially help older adults in Singapore use generative AI (GenAI) chatbots safely and confidently to find and evaluate health information.

The main questions it aims to answer are:

  • Is the conduct of E2NGAGE-Literacy program to improve older adults' AI literacy and digital health literacy feasible?
  • Do older adults find the E2NGAGE-Literacy program acceptable?
  • What are the potential changes in AI literacy, digital health literacy and actual use of AI-chatbot apps and web-based apps between older adults who receive E2NGAGE-Literacy program and those who do not receive the program?
  • What do participants think about E2NGAGE-Literacy, and how can it be improved?

Researchers will compare two groups:

  • E2NGAGE-Literacy group: Participants will join a 6-week program with face-to-face group lessons on using GenAI for health information, supported by online videos, quizzes and short homework tasks.
  • Waitlist control group: Participants will continue with their usual activities at the senior centres and receive the same program after the study period.

Participants in the E2NGAGE-Literacy group will:

  • Join weekly 1.5-hour face-to-face sessions for 6 weeks during the study period
  • Watch short videos and complete online quizzes and practice tasks between sessions during the study period
  • Be invited to a focus group discussion after the program to share their experiences
  • Complete a questionnaire at the start of the study and again at 7 and 12 weeks later
  • Be invited to share AI-chatbot transcripts for analysis

Participants in the waitlist group will:

  • Complete a questionnaire at the start of the study and again at 7 and 12 weeks later
  • Join weekly 1.5-hour face-to-face sessions for 6 weeks after the study period (after week 8)
  • Watch short videos and complete online quizzes and practice tasks between sessions after the study period (after week 12)
  • Be invited to share AI-chatbot transcripts for analysis
Read the detailed description

Artificial intelligence (AI) is rapidly reshaping how health information is produced, distributed and consumed worldwide. Across healthcare systems and consumer markets, AI-enabled technologies - including large language modelling (LLMs) embedded in search engines, conversational agents (e.g., chatbots), recommender algorithms on social media and automated translation tools - are increasingly integrated into everyday information ecosystems. These global trends increase access to plain-language health information and can offer fast, dialogic, concise and tailored medical knowledge, with potential to close gaps in digital health disparities.

Strengthening AI literacy and digital health literacy among older adults is essential to ensure effective and safe use of online health information. AI literacy is the set of competencies that allows one to effectively interact with AI systems (e.g., generate appropriate prompts), critically evaluate AI-generated responses and leverage them as tools to accomplish tasks proficiently and ethically. Digital health literacy extends these competencies to engaging with digital technologies, including GenAI and web-based searches, in effective, safe and helpful approaches to achieve health goals. Together, these literacies can help older adults better differentiate credible from misleading information, communicate more effectively with healthcare providers using information found online, use digital health platforms with confidence and safety, and reduce harmful self-care practices.

Current research on AI literacy among older adults has focused on understanding their experiences, motivation and preferences in learning AI. Despite calls to prioritise community-based digital literacy programs in public health policies and implementation research, tailored interventions on generative AI education programs among adults remain limited and exploratory. Moreover, existing programs for older adults focus on AI literacy and digital health literacy skills in silos and lack the integration of empowering older adults to leverage and apply AI-mediated information to their individual health context.

Based on the findings of the PI's ongoing trial on a digital health literacy intervention conducted among lower-educated older adults, participants showed great interest in learning the use of AI generative chatbots and gained skills on how to evaluate the credibility of online health information.

This study will pilot E2NGAGE-Literacy to explore its potential benefits in improving AI literacy and digital health literacy among community-dwelling older adults. A mixed methods design will be adopted. Sixty older adults aged 60 years and above with limited prior exposure to GenAI will be recruited from active ageing centres of the Tzu Chi Foundation.

The E2NGAGE-Literacy program will last 6 weeks and include weekly face-to-face group lessons, including online videos, quizzes and brief homework tasks. Weekly topics include, but are not limited to, the basics of GenAI chatbots, writing health-related prompts, critically evaluating AI-generated responses, and applying online health information.

Participants in the intervention group may receive additional support where needed. Participants in the waitlist control group will receive the same program after the study period. A subset of participants in the intervention group will join focus group discussions after the program to share their experiences and provide feedback.

Data will be collected at three timepoints: baseline (pre-test), post-test (week 7) and post-test (week 12) to monitor changes in AI literacy, digital health literacy, use of AI chatbots and web-based apps, and other pre-specified outcomes. Quantitative analyses will use repeated measures approaches, and qualitative data will be analysed thematically. Participants will also be invited to share their AI-chatbot transcripts with the research team for further analysis and qualitative data triangulation.

This pilot study will provide insights into the feasibility, acceptability and preliminary changes of E2NGAGE-Literacy as a potentially scalable, culturally responsive intervention to help older adults in Singapore engage with AI-generated health information safely and confidently.

02

Conditions studied

  • Digital Health Literacy
  • AI Chatbot
  • Aged 60 Years or Older

Keywords

  • digital health literacy
  • Artificial intelligence literacy
  • older adults
03

In context

Lead sponsor

National University of Singapore is the lead sponsor of 212 studies on the registry; 54 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
60 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • aged 60 years and above
  • has a smartphone
  • has limited knowledge and exposure to GenAI and internet usage for health information
  • has no cognitive impairment (e.g., screened using the Mini-Cog Test; a score below 3 will be considered a positive screen for possible cognitive impairment or higher risk of dementia)
  • willing to participate and be audio-recorded for qualitative interview

Exclusion criteria

Exclusion Criteria:

  • diagnosed with dementia or cognitive impairment
  • have severe visual or hearing impairments that make it challenging to participate in the intervention group sessions
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
60 participants (estimated)

Study arms

  • Experimental
    E2NGAGE-Literacy Intervention

    Participants in this arm will take part in the E2NGAGE-Literacy program during the study period.

    Behavioral: AI and digital health literacy program (E2NGAGE-Literacy)

  • No intervention
    Waitlist Control

    Participants in this arm will continue with the usual activities provided at their active ageing centres during the study period. They will not receive the E2NGAGE-Literacy program during the study period, and will receive the same program after completing the post-intervention questionnaire.

Interventions

  • BehavioralAI and digital health literacy program (E2NGAGE-Literacy)

    A 6-week program delivered through weekly 1.5-hour face-to-face group lessons, supported by online videos, quizzes and homework on using generative AI chatbots for health information. The programme will be delivered in English and Chinese. Additional support may be provided if needed.

06

What researchers measure

Primary outcomes

  1. Artificial intelligence literacy

    Competency in artificial intelligence (AI) literacy will be measured using the 12-item Artificial Intelligence Literacy Scale (AILS) on a 7-point Likert scale. The AILS includes four domains: awareness (ability to identify and understand AI technology), usage (ability to apply and use AI technology to accomplish tasks proficiently), evaluation (ability to analyse, select and critically evaluate AI applications and their output) and ethics (ability to be aware of the responsibilities and risks associated with the use of AI technology). Internal consistency for the tool is α=0.88, with domains ranging from α=0.73 to 0.78.

    Time frame: Baseline, week 7 (post-test) and week 12 (post-test)

  2. Digital health literacy

    Competency in digital health literacy will be measured using the 24-item Digital Health Literacy Instrument 2.0 (DHLI 2.0). The DHLI 2.0 includes eight domains: operational skills, navigation skills, information searching, evaluating reliability, determining relevance, generating content, using security measures, and protecting privacy. Internal consistency for the tool is α=0.94.

    Time frame: Baseline, week 7 (post-test) and week 12 (post-test)

Secondary outcomes

  1. Actual use of AI chatbot apps and web-based apps

    Measured using self-reported frequency of use and time spent on web browsers, social media platforms, generative AI chatbots and mobile health applications on participants' smartphones.

    Time frame: Baseline, week 7 (post-test) and week 12 (post-test)

  2. Health information orientation

    The 8-item health information orientation scale will be used to measure health information-seeking behaviour style. This five-point Likert scale comprises two domains: information engagement (α=0.66) and information avoidance (α=0.67).

    Time frame: Baseline, week 7 (post-test) and week 12 (post-test)

  3. Motivated learning behaviour

    Measured using an adapted 5-item Motivated Learning Behaviour scale on a 5-point Likert scale, assessing the extent to which participants are willing to work hard and persist in learning AI (α=0.92).

    Time frame: Baseline, week 7 (post-test) and week 12 (post-test)

  4. Perceived usefulness of GenAI chatbots

    Measured using a 4-item adapted subscale from the Technology Acceptance Model 3 tool (α=0.92).

    Time frame: Baseline, week 7 (post-test) and week 12 (post-test)

  5. Perceived ease of use of GenAI chatbots

    Measured using a 4-item adapted subscale from the Technology Acceptance Model 3 tool (α=0.93)

    Time frame: Baseline, week 7 (post-test) and week 12 (post-test)

  6. Trust in health-related information from AI

    Measured using a 3-item adapted trust subscale on a 5-point Likert scale (α=0.91)

    Time frame: Baseline, week 7 (post-test) and week 12 (post-test)

Other outcomes

  1. Participant recruitment

    The speed or proportion at which this study successfully enrolls eligible individuals

    Time frame: Baseline

  2. Retention rate

    The percentage of enrolled individuals who stay in a study and complete all required parts until the end

    Time frame: End of the study (week 12)

  3. Intervention attendance

    The proportion of scheduled or offered weekly intervention sessions that participants actually attend

    Time frame: 6-week intervention

  4. Completion of outcome assessment

    The proportion of enrolled subjects who completed the week 12 data collection

    Time frame: Baseline, week 7 (post-test) and week 12 (post-test)

07

Study locations

No study locations are listed for this record.

08

References and documents

Publications

  • Yang K, Hu Y, Qi H. Digital Health Literacy: Bibliometric Analysis. J Med Internet Res. 2022 Jul 6;24(7):e35816. doi: 10.2196/35816. PubMed 35793141 ↗
  • Milanti A, Norman C, Chan DNS, So WKW, Skinner H. eHealth Literacy 3.0: Updating the Norman and Skinner 2006 Model. J Med Internet Res. 2025 Mar 11;27:e70112. doi: 10.2196/70112. PubMed 40068166 ↗
  • van der Vaart R, Drossaert C. Development of the Digital Health Literacy Instrument: Measuring a Broad Spectrum of Health 1.0 and Health 2.0 Skills. J Med Internet Res. 2017 Jan 24;19(1):e27. doi: 10.2196/jmir.6709. PubMed 28119275 ↗
  • Eskinazi N, Zwilling M, Marques A, Tesler R. The Role of AI in Improving Digital Wellness Among Older Adults: Comparative Bibliometric Analysis. JMIR AI. 2026 Jan 14;5:e71248. doi: 10.2196/71248. PubMed 41540814 ↗
  • Dong Q, Liu T, Liu R, Yang H, Liu C. Effectiveness of Digital Health Literacy Interventions in Older Adults: Single-Arm Meta-Analysis. J Med Internet Res. 2023 Jun 28;25:e48166. doi: 10.2196/48166. PubMed 37379077 ↗

Individual participant data

Plan to share: No — Individual participant data (IPD) will not be shared because this is a small pilot study involving community-dwelling older adults in Singapore. Sharing of IPD is not planned due to privacy, ethical, and institutional data protection requirements under Singapore's Personal Data Protection Act (PDPA) and the National University of Singapore's research data management policies. Only aggregate results will be reported in publications and presentations.

09

Timeline

2 registry updates since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Oct 2026; primary completion for Mar 2027, 5 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 12, 2026
First posted
Oct 19, 2026
StartEst.
Oct 2026
Primary completionEst.
Mar 2027
CompletionEst.
Jul 2027
Last update
Oct 22, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 19, 2026
Show all 2 updates
  1. Oct 22, 2026
    Minor edits only
    + 1 other change: description
  2. Oct 19, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07881510
Collaborators
Buddhist Compassion Relief Tzu-Chi Foundation (Singapore)
Responsible party
Seah Betsy (Betsy Seah, PhD, BSc (Nursing)(Hons), RN, National University of Singapore, Alice Lee Centre for Nursing Studies, National University of Singapore) — Principal investigator
First posted
Oct 19, 2026
Start date
Oct 2026 (estimated)
Primary completion
Mar 2027 (estimated)
Completion
Jul 2027 (estimated)
Last update
Oct 22, 2026

Study contacts

Betsy Seah, PhD, BSc (Nursing)(Hons), RN
Contact
nurseah@nus.edu.sg
6566013213

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion