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NCT07023406: Disfrutando 2

Effectiveness of and Implementation Strategies for 'Disfrutando'.

Not yet recruiting NA Last updated 17 June 2025
What this trial tests

NA trial testing Disfrutando in Type 2 Diabetes Mellitus (T2DM) in 30 participants. Not yet recruiting.

Timeline
1 August 2025
Primary endpoint
15 May 2026
31 July 2026

Quick facts

Lead sponsorUniversity of Missouri-Columbia
PhaseNA
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposeprevention
Enrollment30
Start date1 August 2025
Primary completion15 May 2026
Estimated completion31 July 2026

Drugs / interventions tested

Conditions studied

Sponsor

University of Missouri-Columbia

Who can join

18 and older, any sex, with Type 2 Diabetes Mellitus (T2DM). Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Despite much research that has focused on enhancing type 2 diabetes mellitus (T2DM) health outcomes for high burden populations, more remains to be done. There is a need to develop practical approaches that not only equip people with knowledge about T2DM self-management, but also help them mitigate the adverse social determinants of health (SDOH) that are fueling the burgeoning numbers of people in the United States with T2DM and that are preventing them from practicing healthful behaviors. This study will examine an intervention named 'Disfrutando' that strives to help people prevent and manage T2DM.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Type 2 Diabetes Mellitus (T2DM)

Currently open trials in the same condition.

Other University of Missouri-Columbia trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07023406.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing