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| Name | Class |
|---|---|
| Bolton Clarke Research Institute | UNKNOWN |
| Sunnybrook Research Institute | OTHER |
| North York General Hospital | OTHER |
| King's College London |
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Social isolation and loneliness worsen older peoples' quality of life, risk of dementia, and contributes to 45,000 deaths/year in Canada - as much as smoking. Isolated people use the health care system more often, but have worse outcomes. Effective, inexpensive interventions exist but unfortunately they have not been implemented in Canada.
We partnered with the Australian developer of HOW R U?, an effective and feasible intervention that uses specially trained, older, hospital volunteers to provide peer support to combat isolation and loneliness in isolated older peers.
Little is known about older people's preferences for virtual care (telephone vs. video) nor their relative effectiveness. Thus we will compare two ways of delivering HOW R U: telephone support and a tested, secure user-friendly video conferencing app, aTouch Away® to a common control arm.
We also partnered with Emergency Medicine, Family Medicine, Geriatrics and Psychiatry to identify people who will benefit from peer support; and with Volunteer Services to recruit volunteers.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| HOW RU Intervention delivered by telephone | Experimental | Group Phone will receive the HOW RU? intervention over the telephone. |
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| HOW RU Intervention delivered by video-call | Experimental | Group Video will receive the HOW RU? intervention delivered over video-call using the aTouch Away platform. |
|
| Wait-list Control Group | No Intervention | Control groups will be offered standard care through their referring service (i.e. their routine clinical follow-up). The control group will be offered HOW RU? telephone support outside of the main trial after their primary outcome assessment at 12 weeks |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| HOW R U? Intervention | Other | HOW RU? intervention uses trained volunteer peers to provide strength-based support sessions weekly for 12 weeks. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Change in De Jong Gierveld Loneliness Scale at Baseline | We will use the 6-item De Jong Gierveld loneliness scale as our primary outcome measure.The minimum value is 0 and the maximum value is 6. | This scale will be collected at baseline and at 12 weeks. |
| Measure | Description | Time Frame |
|---|---|---|
| Change in Social Network | Lubben's Social Network Scale | Baseline and at 12 weeks |
| Change in Mood | Geriatric Depression Scale | Baseline and at 12 weeks |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Jacques Lee, MD | Contact | 4168771447 | Jacques.lee@sinaihealth.ca | |
| Joanna Yeung, HBSc | Contact | 6473089440 | Joanna.yeung@sinaihealth.ca |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Mount Sinai Hospital | Recruiting | Toronto | Ontario | M5G 1XS | Canada |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 38199634 | Derived | Lee JS, Rose L, Borgundvaag B, McLeod SL, Melady D, Mohindra R, Sinha SK, Wesson V, Wiesenfeld L, Kolker S, Kiss A, Lowthian J. Impact of a peer-support programme to improve loneliness and social isolation due to COVID-19: does adding a secure, user friendly video-conference solution work better than telephone support alone? Protocol for a three-arm randomised clinical trial. BMJ Open. 2024 Jan 9;14(1):e056839. doi: 10.1136/bmjopen-2021-056839. |
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| ID | Term |
|---|---|
| D012934 | Social Isolation |
| D004630 | Emergencies |
| ID | Term |
|---|---|
| D012919 | Social Behavior |
| D001519 | Behavior |
| D020969 | Disease Attributes |
| D010335 | Pathologic Processes |
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| OTHER |
| University of Toronto | OTHER |
This multi-centered, three-arm, outcome assessor blinded randomized clinical trial will follow CONSORT reporting guidelines and is part of a program of research that adheres to the ORBIT model for developing complex behavioural interventions. In this model, the previous study by Lowthian and colleagues established the proof of concept, and the current trial Phase IIb is adequately powered to test whether two versions of the HOW R U? intervention are effective compared to a common standard care wait-list arm.
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We will use intention-to-treat analysis for the primary outcome to further protect against selection bias. It is not feasible to blind participants to the intervention. Primary outcomes will be assessed after 12 weeks by a research assistant who has had no previous contact with participants and is blinded to the intervention group.
| Change in Quality of life | EQ-5D-5L survey | Baseline and at 12 weeks |
| all-cause mortality | Follow-up phone call at 12 weeks |
| D013568 |
| Pathological Conditions, Signs and Symptoms |