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Social Convoy Palliative Care (Convoy-Pal) Mobile Health for Older Adults

The Usability and Feasibility of Social Convoy Palliative Care (Convoy-Pal) Mobile Health for Older Adults

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04779931
Acronym
ConvoyPal
Enrollment
39
Registered
2021-03-03
Start date
2021-04-01
Completion date
2023-05-30
Last updated
2023-06-18

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

Conditions

Chronic Conditions, Multiple

Brief summary

The aim of this study is to test the feasibility and usability of the Convoy-Pal mobile intervention among older adults. The study is a pilot waitlist control RCT with 40 patients and their convoys randomized to one of two arms: Convoy-Pal intervention or waitlist control. Feasibility will be assessed by recruitment, attrition, and data collection on measures of quality of life and social support. Usability will be captured by self-report usability scales and actual back end utilization data.

Interventions

BEHAVIORALConvoy-Pal

12 week mobile self-management intervention with palliative care resources.

Sponsors

National Institute on Aging (NIA)
CollaboratorNIH
University of Colorado, Denver
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* ≥65 years of age * self-report diagnosis of heart failure (HF) * have multiple chronic conditions (MCC) based on the Disease Burden/Morbidity Assessment by Self-Report (Individuals will be eligible if they self-report the number of diagnosis \> 2 and a disease burden score \>2 indicating the presence of at least two chronic conditions that limit activities of daily of living) * community dwelling in the United States * English speaking

Exclusion criteria

* Self-reported diagnosis of Alzheimer's disease or dementia * Self-reported diagnosis of a severe mental health problem (e.g. schizophrenia, bipolar affective disorder or other psychotic illness) * Participation in community-based palliative care in the last 12 months

Design outcomes

Primary

MeasureTime frameDescription
User Mobile Application Rating Scale12 weeksUsability; 20 items; Range 0-25, Higher score indicates better usability

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026