Could involving family in diabetes education improve blood sugar control?
NCT ID NCT04334109
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This trial tests whether a family-centered diabetes education program helps people with type 2 diabetes manage their blood sugar better than standard education. About 1,100 adults with type 2 diabetes and their family members take part. Participants are randomly assigned to either family education (where family members join sessions) or standard education (where only the patient attends). The main goal is to see changes in HbA1c levels after 12 weeks.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Diabetes self-management education and support (behavioral intervention)
- What this could lead to
- If effective, family-centered diabetes education could improve blood sugar control more than standard education alone.
- What could go wrong
- This is a behavioral study, not a drug trial, so results may vary widely. The primary outcome is short-term (12 weeks), and long-term benefits are uncertain.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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1,100 people
The number who actually took part.
- Started
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Jan 2021
- Finished
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Sep 2024
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * adults ≥18 years of age * have HbA1c ≥ 7.0% * speak English * have a family member/support person willing to take part in the study Exclusion Criteria: * have received formal DSMES in the past three years * have a condition that makes it unlikely for them to be able to follow the study protocol, such as a terminal illness * have plans to move out of the area within 18 months
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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University of Arkansas for Medical Sciences Northwest
Fayetteville, Arkansas, 72703, United States
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