New phone program aims to help overwhelmed caregivers control diabetes
NCT ID NCT04831697
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This pilot study tested a 12-week phone program for 60 African American women aged 40-64 with type 2 diabetes and multiple caregiving responsibilities. Half received extra support for their caregiving stress plus diabetes education, while the other half got standard diabetes education. The goal was to see if the extra support could improve blood sugar control (HbA1c) over 6 months.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Multi-Caregiving Intervention (behavioral support and diabetes education)
- What this could lead to
- If successful, this approach could offer a practical way to help African American women with diabetes and caregiving responsibilities better manage their blood sugar.
- What could go wrong
- This is a small pilot study with only 60 participants, so results may not apply to everyone. The intervention is behavioral, so improvements may be modest or not sustained long-term.
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
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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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60 people
The number who actually took part.
- Started
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Dec 2021
- Finished
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May 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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40 to 64 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: * Age 40-64 years * Self-identifies as female * Self-identifies as African American or Non-Hispanic Black * Self-reports multi-caregiving responsibilities * Clinical diagnosis of T2DM based on HbA1c≥8% at the screening/baseline assessment * Able to communicate in English * Access to a telephone (i.e., landline, mobile device, smart device, etc.) Exclusion criteria: * Mental confusion at screening/baseline assessment suggesting significant dementia, active psychosis, or acute mental disorder * Participation in other diabetes trials * Life expectancy \<6 months based on screening questionnaire
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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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Medical College of Wisconsin
Milwaukee, Wisconsin, 53226, United States
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