NCT03453450

Brief Summary

This study is meant to evaluate the Health TAPESTRY volunteer program. The objective of this study is to explore volunteer experiences in Health TAPESTRY in terms of implementation and to understand how participation in Health TAPESTRY as a volunteer is related to compassion, self-reported physical activity, quality of life, and attitudes toward older adults.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
89

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Mar 2018

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 27, 2018

Completed
6 days until next milestone

First Posted

Study publicly available on registry

March 5, 2018

Completed
8 days until next milestone

Study Start

First participant enrolled

March 13, 2018

Completed
2.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 24, 2020

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 24, 2020

Completed
Last Updated

December 21, 2020

Status Verified

September 1, 2020

Enrollment Period

2.5 years

First QC Date

February 27, 2018

Last Update Submit

December 18, 2020

Conditions

Keywords

Primary Care

Outcome Measures

Primary Outcomes (1)

  • Volunteers' Experiences

    Volunteers' and volunteer coordinators' perceptions about their experiences in Health TAPESTRY overall, and specifically in regards to their understanding of their role; the training that was offered and how it did or did not support them in carrying out their role effectively; the process of engagement in the program from onboarding through the volunteer coordination to conducting home visits with clients; and the perceived outcomes of volunteering, including the impact of volunteering on their own health and wellness. This will be collected through qualitative data: focus groups for volunteers and interviews for volunteer coordinators at the 12-month mark, and volunteer narratives which are written post-client-visits.

    12 months

Secondary Outcomes (7)

  • Compassion satisfaction and compassion fatigue

    Baseline, 3 month, 6 month, 9 month, 12 months

  • Physical Activity

    Baseline, 12 months

  • Quality of Life

    Baseline, 12 months

  • Attitudes Toward Older Adults

    Baseline, 12 months

  • Empathy

    Baseline, 12 months

  • +2 more secondary outcomes

Study Arms (2)

Health TAPESTRY volunteers

Volunteers in a primary care setting connecting with Health TAPESTRY clients

Health TAPESTRY Volunteer Coordinators

The coordinators of volunteers

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Study participants are drawn from the Health TAPESTRY volunteer pool. All Health TAPESTRY volunteers will be invited into the evaluation, however only those volunteers who choose to take part in the evaluative component of the program will be included in the analysis. Although we aim to include as many Health TAPESTRY volunteers as possible, an achievable target is set at half of the volunteers (approximately 17) in each of the 6 sites being involved in the research component. The Volunteer Coordinator (VC) in each site will also be invited to attend an interview. The day-to-day management of volunteers within each site is managed by a VC from the Canadian Red Cross. The VC is the first contact for volunteers, and also the primary conduit that connects volunteers with clients.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

David Braley Health Sciences Centre, McMaster University

Hamilton, Ontario, L8S 4K1, Canada

Location

Study Officials

  • Doug Oliver, MSc,MD,CCFP

    McMaster University

    PRINCIPAL INVESTIGATOR
  • Dee Mangin, MBChB,DPH,FRN

    McMaster University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
OTHER
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 27, 2018

First Posted

March 5, 2018

Study Start

March 13, 2018

Primary Completion

September 24, 2020

Study Completion

September 24, 2020

Last Updated

December 21, 2020

Record last verified: 2020-09

Data Sharing

IPD Sharing
Will not share

Locations