Fact CheckerSign in

NCT07120334Recruiting

Mobile Health Dietary Intervention for Stroke Survivors With Prediabetes or Type 2 Diabetes

mHealth Dietary Intervention for Stroke Survivors With Prediabetes or T2D

Source: ClinicalTrials.gov · Last updated 21 Jan 2026

Brief summary (registry, in English)

Objectives: This study aims to test whether a mobile app called PortionSize Ed can help adults who have had a recent stroke and also have prediabetes or type 2 diabetes improve their diet. Specifically, we want to see if the app can help people follow a Mediterranean-style diet, which may lower the risk of future strokes and improve overall health. The main goals are to: * Test if the app is easy to use and acceptable to participants. * See whether the app helps people follow a healthier diet. * Look at changes in health indicators like blood sugar, cholesterol, blood pressure, and body fat. Design and Outcome: This is a randomized controlled pilot study that will involve 40 participants. All participants will be recruited from Queen's Medical Center after a recent stroke and will be randomly assigned to one of two groups: Intervention Group: Uses the full PortionSize Ed app, gets weekly reminders and educational videos, and has 3 sessions with a registered dietitian (RDN) over 12 weeks. Control Group: Uses a basic version of the app without feedback or RDN support, and receives usual care for stroke recovery. All participants will continue to receive standard care from Queen's, including the My Stroke Recovery Guide. The study lasts 12 weeks, with visits at the beginning and end to collect health data and feedback on the app. Schedule and Type of Evaluations/Interventions: Participants will complete the following: Baseline and Week 12 Visits: In-person assessments for blood sugar (HbA1c), cholesterol, blood pressure, height, weight, and body composition (using DXA, BIA, and 3D imaging), as well as surveys about their diet and activity levels. Intervention Group Only: * Three virtual counseling sessions with a registered dietitian (Week 1, 6, 12) * Weekly nutrition goal tracking and texting with the dietitian * Watching short educational videos through the app * Receiving app-based feedback on how well their diet follows Mediterranean Diet recommendations Duration of Study: The study will last 12 weeks for each participant, with an optional long-term follow-up using medical records. Sample Size and Population: The study will include 40 adults, ages 30 to 65, who: * Recently experienced a stroke * Have a history of prediabetes or type 2 diabetes * Are medically stable and able to use a smartphone (or willing to use a study-provided iPhone) * People will be excluded if they have severe swallowing issues, cognitive problems, or dietary needs that would make it hard to follow a Mediterranean-style diet.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
40 (estimated)
First submitted
28 Jul 2025
Start date
1 Feb 2026
Primary completion date
31 Dec 2026
Lead sponsor
University of Hawaii
NCT number
NCT07120334

What you commit to

  • Study type: Interventional
  • Planned participants: 40
  • From 1 Feb 2026 to the primary completion date, 31 Dec 2026
  • 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.

Other illness

  • Type 1 diabetes
  • Cognitive impairment (e.g., dementia, post-stroke confusion) that precludes consent or compliance, as judged by the clinical care team
  • Serious comorbid conditions that, in the opinion of the

Other

  • Severe dysphagia that prevents oral intake
  • Current participation in another interventional clinical trial
  • Pregnant or breastfeeding, or planning to become pregnant during the study period
  • Unwilling or unable to provide written informed consent

Who the study is looking for

  • Aged 30 to 65 years
  • Recent stroke (ischemic, hemorrhagic or Transient Ischemic Attack), within 1-14 days prior to enrollment
  • Confirmed diagnosis of prediabetes or type 2 diabetes, based on HbA1c results
  • Medically stable and cleared for oral diet and physical activity by the attending physician
  • Cleared for thin liquids and regular textures by physician
  • Capable of providing informed consent
  • Able to speak and read English
  • Owns a smartphone OR is willing to use a study-provided iPhone
  • Has sufficient cognitive and physical function to use a mobile app
  • Willing to participate in all study procedures and available for the 12-week duration

Age in the registry: 30 years to 65 years · Sex: All · Does not accept 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 Hawaii Cancer Center
Coordinator of this site? Confirm its status
HonoluluUnited StatesRecruiting

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