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An Exploratory Feasibility Study

AI-Enhanced Educational Intervention to Support Contextual Well-being in Young Adults (ContextWell)

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07009964
Acronym
Contextwell
Enrollment
12
Registered
2025-06-08
Start date
2025-11-01
Completion date
2026-02-01
Last updated
2025-06-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Behavior and Behavior Mechanisms, Lifestyle, Healthy, Well-Being, Young Adult

Keywords

Student well-being, Artificial Intelligence, Contextual Well-being, Contextual AI, Preventive health, Digital Health, Lifestyle medicine, Pilot study, Proof of concept

Brief summary

This study explores the feasibility of ContextWell, a well-being education programme that combines an online webinar with an AI-powered behavioural nudging system. The programme aims to support university students, particularly those in healthcare disciplines, in enhancing well-being and adopting healthier lifestyle habits. The primary objective is to determine whether the programme can be feasibly delivered within university settings. A secondary objective is to assess its potential to improve student well-being and encourage behavioural changes aligned with lifestyle medicine principles. The intervention builds on the understanding that healthcare professionals' lifestyle habits and well-being have a direct impact on patient care. Focusing on healthcare students helps advance the integration of lifestyle medicine within health education and clinical practice. This single-group feasibility study delivers the full intervention to all participants. Students participate in an online well-being webinar and receive AI-generated behavioural prompts designed to promote self-awareness and healthier daily choices. Key evaluation measures will indicated the feasibility of the programme among young adults in academic environments. Participant feedback and initial outcomes will support future development and inform larger-scale research.

Interventions

OTHERContextWell Educational Programme

ContextWell Educational Programme

Sponsors

UCD Clinical Research Centre, Ireland
CollaboratorUNKNOWN
University College Cork
CollaboratorOTHER
Imperial College London
CollaboratorOTHER
University College Dublin
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

Primarily healthcare students, young adults enrolled in higher education (18-30 years old) Access to a computer or mobile device with an internet connection; Willingness to participate in the educational webinar; Willingness to complete AI-driven assignments; Able to read and understand English.

Exclusion criteria

Are under the age of 18, or above 30; Inability to access a computer or mobile device with internet connection; Inability to read or understand English; Unwillingness to participate in the webinar or complete assignments.

Design outcomes

Primary

MeasureTime frameDescription
Recruitment RateUp to 4 weeks post-study launch (enrolment period).Description: Proportion of eligible participants who enroll in the ContextWell Programme. Metric: % of enrolled participants out of those approached. Measurement Method: Screening and enrolment logs.
Retention RateThrough study completion, an average of 5 weeks post-baseline.Proportion of enrolled participants completing the programme. Metric: 1. % completing final follow-up. 2. Count completing all study components. Measurement Method: Attendance records, programme tracking data, follow-up survey.

Secondary

MeasureTime frameDescription
Acceptability of the InterventionAt 2 weeks post-intervention.Description: Participants' satisfaction with the content, format, and delivery. Metric: Mean satisfaction rating; qualitative feedback. Measurement Method: Post-intervention survey (Likert-scale + open-ended items).
Demand for the ProgrammeAt 2 weeks post-intervention.Participants' expressed interest in continued use and peer recommendation. Metric: % intending to continue use or recommend. Measurement Method: Survey responses on future use/recommendation.
Implementation FeasibilityDuring intervention period, Weeks 1 to 3 post-baseline.Practicality of delivering the intervention as planned. Metric: Number of technical issues. % of content delivered as intended. Measurement Method: Researcher logs, participant feedback.
Perceived Impact on Well-BeingAt 4 weeks post-baseline.Participants' perception of effects on well-being Metric: % reporting improved well-being. Measurement Method: follow-up survey (Likert-scale and reflections).

Countries

Ireland

Contacts

Primary ContactYao Xie
toyaoxie@gmail.com0868928972
Backup ContactJohn Broughan
john.broughan@ucd.ie

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026