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NCT06384521Withdrawn

Lifestyle MIND- Feasibility of Wait-list Control

Type 2 Diabetes Prevention and Management for People With Serious Mental Illness: A Feasibility Study

Source: ClinicalTrials.gov · Last updated 12 Mar 2026

Reason given: No funding obtained

Brief summary (registry, in English)

The goal of this clinical trial is to examine if it is feasible to randomly assign people into two groups and participate in Lifestyle MIND (Mental Illness and/N' Diabetes) at two different times. Lifestyle MIND is a diabetes lifestyle intervention recently developed for people with serious mental illness (SMI). It is known to be helpful for people with SMI who complete it, but the investigators do not know the effect in comparison to those who do not participate in it. The main questions it aims to answer are: * Does Lifestyle MIND improve diabetes control among people with SMI? * Will the effect of Lifestyle MIND be sustained 10 weeks after program completion? * From the provider's perspective, what are the barriers of achieving optimal diabetes treatment outcomes for patients with SMI? Researchers will compare outcomes of participants in the intervention with those in the wait-list control arm, to see if there will be significant differences in blood glucose level, compliance of diabetes self-management, time staying active, number of emergency department (ED) visits and psychiatric hospitalization, and subjective well-being.

Status (registry)
Withdrawn
Study type
Interventional
Enrollment
0 (actual)
First submitted
22 Apr 2024
Start date
Dec 2025
Primary completion date
Jul 2027
Lead sponsor
The University of Texas Health Science Center at San Antonio
NCT number
NCT06384521

Who cannot take part

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

Other

  • unable to perform the moderate intensity exercise program in Lifestyle MIND

Who the study is looking for

  • a diagnosis of SMI
  • a diagnosis of T2DM, seeing a health care provider for T2DM, or having been informed by a healthcare provider for being pre-diabetic or diabetic
  • willingness to commit to participate for 20 weeks
  • ability to respond to self-report scales and questionnaires used in the study

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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SiteCityCountrySite status
University of Texas Health Science Center at San AntonioSan AntonioUnited StatesUnknown status

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