Skip to content

myHealthHub for Older Adult Inpatients

myHealthHub for Older Adult Inpatients to Lower Loneliness and Improve Patient Engagement, Quality of Life and Mental Health

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05450445
Enrollment
0
Registered
2022-07-08
Start date
2022-09-01
Completion date
2023-09-01
Last updated
2025-07-10

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

Conditions

Loneliness, Patient Engagement, Quality of Life, Stress

Keywords

Older adults, Hospital Inpatients, Technology

Brief summary

This study will assess myHealthhub in hospitalized older adults throughout 5 days of their hospital stay. The investigators propose a mixed method randomized controlled trial (RCT) comparing myHealthHub platform vs. a simplified HealthHub system that provides only TV access, in order to evaluate patients' loneliness, stress, quality of life, patient engagement, and other mental health outcomes in n=60 older adult inpatients. The investigators will also use qualitative methods to assess user and stakeholder experience, and engagement.

Interventions

DEVICEmyHealthHub

myHealthHub is a multimodal patient engagement platform delivered on bedside terminals to provide hospital inpatients with social connection, meal ordering services, entertainment (TV, etc.), and access to medical care team.

DEVICETV-only

myHealthHub device equipped with the TV-only entertainment option.

Sponsors

Lady Davis Institute
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Quantitative Component: Inclusion Criteria: * ≥60 years old * Admitted to non-surgical hospital unit * Speak English or French * Capable of giving consent

Exclusion criteria

* Delirium * Active suicidal ideation * Moderate/severe dementia diagnosis Qualitative Component: Inclusion Criteria: * Participants from quantitative component * Hospital staff, nurses, clinicians facilitative use of the service * ≥18 years old * Speak English or French

Design outcomes

Primary

MeasureTime frameDescription
Changes in LonelinessBaseline, day 2, day 3, day 4, day 5Loneliness measured by the UCLA 3-item Loneliness Scale (UCLA-3). This is a 3-item scale with scores ranging from 3-9, with higher scores indicating greater severity of loneliness.

Secondary

MeasureTime frameDescription
Changes in StressBaseline, day 3, day 5Stress measured by Perceived Stress Scale (PSS). This is a 14-item scale with scores ranging from 0-56, with higher scores indicating greater severity of stress.
Changes in Patient EngagementBaseline, day 3, day 5Patient engagement measured by Patient Activation Measure-13 (PAM-13). This is a 13-question scale.
Changes in Quality of Life in Older AdultsBaseline, day 3, day 5Quality of life which will be measured by the Euro-Quality of Life (EQ-5D). This is a 5-component scale including mobility, self-care, usual activities, pain/discomfort, and anxiety/depression.

Other

MeasureTime frameDescription
Exploratory Outcome: Changes in AnxietyBaseline, day 5Anxiety measured by Generalized Anxiety Disorder-7 (GAD-7) scale. This is a 7-question scale with scores ranging from 0-21, with higher scores indicating greater severity of anxiety.
Feasibility Outcome: EnrollmentDay 5Enrollment rate (percent of participants enrolled from eligible participants)
Qualitative Component: Semi-structured interviewsDay 5The qualitative outcome of this RCT will analyze the experiences, barriers, and engagement of older adults with the myHealthHub device. It will also explore the experiences and limitations of hospital support staff with myHealthHub service.
Feasibility Outcome: RecruitmentDay 5Recruitment target (ability to recruit 60 participants)
Feasibility Outcome: RetentionDay 5Retention rate (percent of randomized participants who complete 5-day assessments in both arms)
Exploratory Outcome: Changes in DepressionBaseline, day 5Depression measured by the Patient Health Questionnaire-9 (PHQ-9). This is a 9-question scale with scores ranging from 0-27, with higher scores indicating greater severity of depression.

Outcome results

None listed

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