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Interprofessional Community-Based Diabetes Intervention for Older Adults

McMaster University logo

McMaster University

Status

Completed

Conditions

Diabetes Mellitus, Type 2

Treatments

Other: Home visits and group program

Study type

Interventional

Funder types

Other

Identifiers

NCT01880476
Labarge-13-377

Details and patient eligibility

About

This study will examine the feasibility and acceptability of a 6-month interprofessional community-based health promotion program, and explore its effects on older adults' self-management of Type 2 Diabetes (T2DM). Recently enrolled clients of Diabetes Care Guelph (DCG), who are age 65+ and have at least two other chronic conditions, will be eligible to participate. Participants must be English speaking, community-dwelling, independent in activities of daily living, and mentally competent to give informed consent. The 6-month intervention will consist of: in-home visits by a Registered Nurse and Registered Dietitian from DCG; participation in a monthly Diabetes Wellness Day group program offered through the Guelph Wellington Seniors Association (GWSA) together with DCG; peer support from trained volunteers at the Diabetes Wellness Day group program; care coordination by the DCG Registered Nurse to help participants access necessary supports and services; and monthly team conferences between care providers at DCG and the GWSA to develop a client-centred plan of care. To evaluate the program, participants will complete interviewer-administered questionnaires before and after the intervention, and care providers and peer volunteers will take part in group interviews.

Enrollment

45 patients

Sex

All

Ages

65+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Age 65+
  • Referred to Diabetes Care Guelph within the past 12 months
  • At least two chronic conditions in addition to Type 2 Diabetes Mellitus
  • English speaking
  • Community-dwelling, in the city of Guelph
  • Independent in activities of daily living
  • Mentally competent to provide informed consent

Trial design

Primary purpose

Health Services Research

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

45 participants in 1 patient group

Home visits and group program
Experimental group
Treatment:
Other: Home visits and group program

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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