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Clinical Trials/NCT02158741
NCT02158741
Completed
Not Applicable

A Client-Driven Intervention to Support Self-Management Among Community-Living Older Adults With Type 2 Diabetes and Multiple Chronic Conditions

McMaster University8 sites in 1 country291 target enrollmentSeptember 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Type 2 Diabetes Mellitus
Sponsor
McMaster University
Enrollment
291
Locations
8
Primary Endpoint
Summary of Diabetes Self-Care Activities
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The overall purpose of this research is to examine and compare the effectiveness and costs of a community-based intervention to support self-management with usual primary care for older adults with Type 2 Diabetes Mellitus and multiple chronic conditions and their family caregivers. Once the study is complete, the investigators will be able to determine if there is any measurable difference in self-care management between usual care plus the intervention versus usual care alone.

Detailed Description

Research Goal To examine the comparative effectiveness and costs of a community-based intervention to support self-management with usual primary care for older adults with T2DM and Multiple Chronic Conditions and their family caregivers. Objectives 1. To determine if a 6-month, IP, community-based intervention improve self-management compared with usual primary care services? 2. To compare the effectiveness of the intervention on HRQoL, physical activity, nutritional status, depression, anxiety, diabetes parameters (blood glucose levels \[HbA1c, hypoglycemic episodes\]), diabetes-related complications, number of vascular events, social support number of falls, fall risk and medication safety with usual primary care services? 3. To determine the effectiveness of the intervention on HRQoL of family caregivers compared with usual primary care? 4. To assess whether or not the intervention improves clinical practice behaviours? 5. To determine the 6-month costs of use of health services of the intervention compared with usual care, from a social perspective? 6. To identify which subgroups of older adults with T2DM and MCC benefit most from the intervention? 7. To determine the effectiveness of the intervention based on sex/gender and region? 8. To determine the overall feasibility and acceptability of an IP community-based health promotion intervention and what can be identified as barriers and facilitators to implementation?

Registry
clinicaltrials.gov
Start Date
September 2014
End Date
May 2017
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Maureen Markle-Reid

RN, PhD, Scientific Director

McMaster University

Eligibility Criteria

Inclusion Criteria

  • older adults aged 65+
  • live in the local vicinity of a participating Diabetes Education Program
  • were referred to their Diabetes Education Program within the past 24 months
  • competence in English (or access to a translator)
  • intention to continue living in the area for the next 6 months
  • two reported chronic conditions in addition to T2DM. Individuals with newly diagnosed T2DM as well as those who were already receiving treatment for T2DM will be eligible for inclusion in the study.

Exclusion Criteria

  • score of 20 or less in Montreal Cognitive Assessment (MoCA) test AND without access to a substitute decision maker to sign consent (Score of 20 or less is not in itself an exclusion).

Outcomes

Primary Outcomes

Summary of Diabetes Self-Care Activities

Time Frame: Every two months from study onset until the end of study (6 months from baseline)

The SDSCA is a multidimensional measure of diabetes self-management with adequate internal and test-retest reliability, and evidence of validity and sensitivity to change. The revised SDSCA consists of items that assess the following aspects of the diabetes regimen: general and specific diet, exercise, blood-glucose testing, foot care, and smoking. Scores are calculated for each of these five regimen areas. This data is collected by the interventionists at each visit.

Secondary Outcomes

  • SF12v2(Baseline and end of study (6 months from baseline))

Study Sites (8)

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