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NCT04334109Completed

Comparative Effectiveness of Family DSMES and Standard DSMES Among Diverse Populations

Source: ClinicalTrials.gov · Last updated 22 Jun 2026

Brief summary (registry, in English)

The investigators conducted a comparative effectiveness randomized controlled trial comparing a family model diabetes self-management education and support intervention (Family-DSMES) and a standard model DSMES intervention (Standard-DSMES). The trial included 550 persons with type 2 diabetes mellitus (PWD) and 550 of their family members/support persons. PWD were randomly assigned to either the Family-DSMES arm or the Standard-DSMES arm. In the Family-DSMES arm, the family members/support persons of the PWD took part in the educational sessions. In the Standard-DSMES arm, the family members/support persons did not participate in educational sessions or goal setting. Both interventions were delivered in a group setting via telehealth. Baseline, immediate post-intervention (12 weeks) and 6 months post-intervention data were collected from PWD and family members/support persons in both study arms. In both study arms, we obtained a medical records release to abstract the primary outcome at 12 months post-intervention and 18 months post-intervention for PWD. The primary outcome was change in Hemoglobin A1c between baseline and immediate post-intervention among PWD.

Status (registry)
Completed
Study type
Interventional
Enrollment
1100 (actual)
First submitted
26 Mar 2020
Start date
4 Jan 2021
Primary completion date
17 May 2023
Lead sponsor
University of Arkansas
NCT number
NCT04334109

What you commit to

  • Study type: Interventional
  • Participants enrolled: 1100
  • From 4 Jan 2021 to the primary completion date, 17 May 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • have received formal DSMES in the past three years

Other illness

  • have a condition that makes it unlikely for them to be able to follow the study protocol, such as a terminal illness

Other

  • have plans to move out of the area within 18 months

Who the study is looking for

  • adults ≥18 years of age
  • have HbA1c ≥ 7.0%
  • speak English
  • have a family member/support person willing to take part in the study

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Arkansas for Medical Sciences Northwest
Coordinator of this site? Confirm its status
FayettevilleUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.