Changes in Person-reported Outcomes and Behavior Using the Accu-Chek SmartGuide CGM and Predict App
- NCT ID
- NCT07814508
- Registry status
- Recruiting
- Study type
- Not specified in the registry data
- Phase
- Not applicable
- Sponsor
- FIDAM RDC
Overview
ClinicalTrials.gov lists this study as Recruiting.
Enrollment: 89 participants (Estimated).
What is being studied
No interventions are listed in the registry data.
Who may be eligible
- Ages
- Not specified in the registry data
- Sex
- Not specified in the registry data
- Healthy volunteers accepted
- No
ClinicalTrials.gov lists the following eligibility criteria.
Inclusion Criteria:
* Type 1 diabetes or Type 2 diabetes with intensified insulin therapy (defined as basal-bolus therapy with self-adjustment of bolus doses)
* CGM use during the past 3 months (without predictive features)
* Age ≥ 18 years
* HbA1c \< 10%
* Informed consent
Exclusion Criteria:
* Use of the SmartGuide CGM solution
* AID use
* Current treatment with psychiatric medications
* Diabetes duration \< 3 months
* Current or planned pregnancy
* Peripheral neuropathy that will impact sleep quality according to the judgement of the participant
* Severe complications (e.g. kidney disease, cancer)
Study locations
1 study location is listed.
Site recruitment status is not specified in the registry data for these locations.
Countries: Germany
- Baden-Wurttemberg, Germany: 1
Sample of listed locations
- Fidam Rdc — Bad Mergentheim, Baden-Wurttemberg, 97980, Germany — Site recruitment status not specified in the registry data
Study details
- Start date
- February 1, 2026
- Primary completion date
- October 31, 2026
- First posted
- September 11, 2026
Source and update information
- Source
- ClinicalTrials.gov
- NCT ID
- NCT07814508
- Registry last updated
- September 11, 2026
- QualifiedStudies registry data refreshed
- September 21, 2026
View NCT07814508 on ClinicalTrials.gov
Trial information can change. Confirm current study details with the study team or the registry.
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