Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 2:36 AM
Ignite Modification Date:
2025-12-25 @ 2:36 AM
NCT ID:
NCT07120334
Eligibility Criteria:
Inclusion Criteria:
* Aged 30 to 65 years
* Recent stroke (ischemic or hemorrhagic), 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
Exclusion Criteria:
* Severe dysphagia that prevents oral intake
* Type 1 diabetes
* Cognitive impairment (e.g., dementia, post-stroke confusion) that precludes consent or compliance, as judged by the clinical care team
* 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
* Serious comorbid conditions that, in the opinion of the
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
30 Years
Maximum Age:
65 Years
Study:
NCT07120334
Study Brief:
Protocol Section:
NCT07120334