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| ID | Type | Description | Link |
|---|---|---|---|
| OT2HL158287 | U.S. NIH Grant/Contract | View source |
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| Name | Class |
|---|---|
| National Heart, Lung, and Blood Institute (NHLBI) | NIH |
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In a 3-group trial with randomization and follow-up for 12 months, we will compare use of the VSC as well as health and quality of life outcomes among 650 older adults in St. Louis who receive either: (1) home delivered meals AND a GrandPad; (2) home-delivered meals but no GrandPad for 6 months; and (3) in person meals at senior center but no GrandPad.
The aims of the study are:
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| GrandPad1 | Experimental | This group will receive a GrandPad right away after they complete the baseline survey |
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| GrandPad2 - 6mo | Other | Delayed interventional. This group will receive a GrandPad after 6 months. |
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| Congregate | Active Comparator | This group will not receive a GrandPad but will get access to the Virtual Senior Center |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Virtual Senior Center - GrandPad | Behavioral | The Virtual Senior Center engages older adults in programs and services online with the help of a GrandPad. |
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| Measure | Description | Time Frame |
|---|---|---|
| The Social Isolation Scale in Older Adults (Nicholson et al., 2020; The Gerontologist) | This 6-item questionnaire measures the extent to which an individual feels socially unconnected, using 2 related constructs (3 items per construct): quantity of social contacts and sense of relationship. The response options for social contacts ranges from 1 (none) to 5 (6 or more) and the sense of relationship ranges from 1(strongly disagree) to 5 (strongly agree). The possible summed scores range from 6 to 30, with higher scores indicating less social isolation. | 12 month |
| Measure | Description | Time Frame |
|---|---|---|
| Digital Social Participation (Anderberg et al., 2021; JMIR) | This 6-item questionnaire measures extent to which someone feels that digital technology is beneficial in their life. Response options range from 1 (strongly disagree) to 5 (strongly agree), so total summed scores range from 6 -30. A higher scores indicates more positive perceptions of digital technology. | 12 month |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Matthew Kreuter, PhD, MPH | Washington University School of Medicine | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Washington University | St Louis | Missouri | 63101 | United States |
The raw survey response data including dates collected, as well as participant ID codes generated for this study will be shared in order to link the five waves of survey data as well as documentation of participation. All respondent identifiers (e.g., names, addresses) will be removed before sharing. Final de-identified intervention data and Common Survey 4 data will be shared with the CEAL (community engagement Alliance) Technical Assistance Team. Other CEAL researchers will be allowed to request common survey data.
We will share all publicly accessible files on WashU Research Data, an institutional repository managed by the Washington University in St. Louis Libraries that uses a cloud-based hosted repository service called TIND as its platform. TIND is based on the open-source Invenio software developed at the research institute CERN to manage its own scholarly output. TIND uses an OAIS-compliant approach to preservation, with redundancy backup, conversion to archival file format
3/31/28 - indefinitely
Users must register with the repository and agree to the License specified for the project. This license will allow users to adapt and build upon the materials in any format for noncommercial purposes only and so long as attribution is given to the original creators and grant funding. Any adapted or new data formats and accompanying descriptions will also need to be publicly available under identical terms as the original. Additionally, the license will protect study participants by limiting data use to scientific research and aggregate statistical reporting, prohibit attempts to identify study participants, and require immediate reporting of any identification of study participant's identity. Data users also agree not to share or redistribute any data downloads.
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Participants in 2 of the groups will be randomly assigned to receive the intervention immediately or in 6 month. The 3rd groups is naturally occurring comparison.
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Though participants and investigators won't know condition of the randomized groups upon enrollment, they will know when they receive the GrandPad. The 3rd group will not be masked at any point.
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| Virtual Senior Center - No GrandPad | Behavioral | Participants will be given information to access the website when they are able from their own phone, tablet, or computer. |
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