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SMARTCLOTH. Design, Implementation and Study of the Effectiveness and Usability of a Digital Tablecloth for Self-management of Diet in Diabetic Patients.

M

Maimónides Biomedical Research Institute of Córdoba

Status

Invitation-only

Conditions

Diabetes Mellitus Type 2
Diabetes Mellitus Type 1

Treatments

Device: SMARTCLOTH

Study type

Interventional

Funder types

Other

Identifiers

NCT06623708
PI21/01602

Details and patient eligibility

About

The objective of this clinical trial is to know the usability and efficacy of SMARTCLOTH for better control and adherence to the dietary patterns recommended to patients with diabetes, both the portion diet system (more common for cases of Diabetes Mellitus type 1 -DM1-), and the plate method (more recommended in cases of Diabetes Mellitus type 2-DM2-). The main questions are:

  • Does the use of SMARTCLOTH improve glycemic control in patients with diabetes mellitus?
  • Do patients with diabetes mellitus find SMARTCLOTH useful in their daily lives?

The researchers will compare changes over 3 months in variables related to glycemic control in two groups, one using SMARTCLOTH (intervention group) and the other following standard recommendations (control group). To do so, participants will have to:

  • Use SMARTCLOTH for 3 months or follow the recommendations they receive from their referring health professionals.
  • Come back after three months for a check-up of the chosen variables.
  • The experimental group should contact the investigators in case the hardware has any problems.

Enrollment

90 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria: Subjects with type 1 and 2 diabetes (eligible population) aged between 18 and 70 years with disease progression not exceeding 15 years and HbA1c greater than 7.5.

Exclusion Criteria:

  • Degree of dependence (physical or psychological) that makes it impossible for them to perform autonomous self-care of the dietary-nutritional regimen.
  • Oncological or autoimmune disease, chronic renal insufficiency, transplant patients and others that alter the values of the result variables or may constitute a confounding factor.
  • Other diseases that entail surgical interventions or hospital admissions that make it impossible to follow up the study.
  • Patients with complications due to the evolution of the diabetic pathology: retinopathy, nephropathy, polyneuropathy, ischemic heart disease, as well as other micro and macrovascular complications derived from the same and already recorded in the patient.
  • Those subjects subjected to specific dietary regimes such as celiac disease, lactose intolerant, etc.

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

90 participants in 2 patient groups

Control
No Intervention group
Description:
This group of participants should follow the general recommendations for the management of Type 1 or Type 2 Diabetes.
SMARTCLOTH
Experimental group
Description:
This group will use SMARTCLOTH for 3 months.
Treatment:
Device: SMARTCLOTH

Trial contacts and locations

5

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Data sourced from clinicaltrials.gov

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