UNISCREEN: Universal Capillary Screening for Chronic Autoimmune, Metabolic and Cardiovascular Diseases: Feasibility and Acceptability Pilot Study.

Sponsor
Emanuele Bosi (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05841719
Collaborator
Italian Diabetes Foundation (Other)
3,095
1
9.4

Study Details

Study Description

Brief Summary

This study represents a model for a public health program based on a general population screening for the most prevalent chronic metabolic, cardiovascular and autoimmune diseases across adulthood, childhood and adolescence. The main purpose is to assess feasibility and acceptability of using a capillary screening for this purpose. Secondly, it will be possibile to identify people at increased risk of developing one of these health conditions as well as those who are at pre-symptomatic clinical stages. Risk assessment is needed to identify prevention strategies; early diagnosis allows to start early treatment interventions aimed at reducing lifetime complications.This interventional study will enroll volunteers from Cantalupo, a locality belonging to the Municipality of Cerro Maggiore (Milan). Participants will be offered to undergo two capillary blood sampling to test blood glucose levels, glycated haemoglobin, total cholesterol, HDL-c, LDL-c, triglycerides and specific antibodies for type 1 diabetes and celiac disease. In case a participant screens positive for type I diabetes and/or celiac disease, they will be subsequently invited to undergo a new confirmatory blood draw on venous blood. Blood pressure will be also measured for each participant

Condition or Disease Intervention/Treatment Phase
  • Other: Screening test
N/A

Detailed Description

This is a low-risk, single-center, interventional study, assessing whether capillary screening for an early staging of the most prevalent chronic metabolic, cardiovascular and autoimmune diseases is feasible at a population-based level. The study will enroll volunteers from Cantalupo, a locality of 3095 inhabitants belonging to the Municipality of Cerro Maggiore (Milan). The main purpose is to assess feasibility and acceptability of using this public intervention. Secondary outcomes are: (i) measurement of the specific disease markers; (ii) estimation of the prevalence of the identified diseases within the population; (iii) estimation of the prevalence of the identified diseases across age classes; (iv) correlation of study disease indicators with demographics, anthropometrics and clinical data of the population , v) multiparametric risk assessment. Participants will be offered to undergo a capillary blood sampling to test blood glucose levels, glycated haemoglobin, total cholesterol , HDL-c, LDL-c, triglycerides, Glutamic Acid Decarboxylase (GADA), Insulinoma-Associated-2/Tyrosine Phosphatase (IA-2A), Insulin (IAA), Zinc Transporter-8 Autoantibodies (ZnT8A) for type I diabetes and tissue transglutaminase antibodies for celiac disease. Glucose and lipid blood levels will be detected at the time of the screening. The results of autoantibodies research for celiac disease and type 1 diabetes will be available within a few days. In case a participant screens positive for type I diabetes and/or celiac disease, they will be subsequently invited to undergo a new confirmatory blood draw on venous blood. Blood pressure will be also measured for each participant.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
3095 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
capillary samplingcapillary sampling
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
General Population Universal Capillary Screening for Chronic Autoimmune, Metabolic and Cardiovascular Diseases (UNISCREEN): Feasibility and Acceptability Pilot Study.
Anticipated Study Start Date :
Apr 22, 2023
Anticipated Primary Completion Date :
Dec 31, 2023
Anticipated Study Completion Date :
Feb 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Other: Population from Cantalupo, locality of the Municipality of Cerro Maggiore (MI).

capillary sampling and questionnaires to test feasibility and acceptability

Other: Screening test
Capillary blood sampling by finger-prick devices and second confirmatory venous sampling when needed.

Outcome Measures

Primary Outcome Measures

  1. feasibility and acceptability [through study completion, an average of 1 year]

    To assess feasibility and acceptability of the screening program

Secondary Outcome Measures

  1. blood glucose and lipids level (mg/dl) [through study completion, an average of 1 year]

    Capillary blood sampling will be performed by finger-prick devices.

  2. IAA, GADA65, ZnT8, IA2 autoantibodies (U/ml) [within a few days]

    Capillary blood sampling will be performed by finger-prick devices.

  3. anti-transglutaminase autoantibodies (UA) [through study completion, an average of 1 year]

    Capillary blood sampling will be performed by finger-prick devices.

  4. systolic and diastolic blood pressure (mmHg) [through study completion, an average of 1 year]

    Blood pressure measurement will be performed through a sphygmomanometer.

  5. HbA1c (mmol/mol) [through study completion, an average of 1 year]

    Glycated hemoglobin will be measured by finger-prick devices.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion criteria:
  • Residency in Cantalupo, locality of the Municipality of Cerro Maggiore (MI)

  • Age between 1 and 100 years

  • Ability to understand the purpose of the project and to sign the informed consent.

Exclusion criteria:

No exclusion criteria.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Emanuele Bosi
  • Italian Diabetes Foundation

Investigators

  • Principal Investigator: Emanuele Bosi, MD, San Raffaele Institute

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Emanuele Bosi, MD, Professor of Internal Medicine, Head, General Medicine, Diabetes & Endocrinology, IRCCS San Raffaele
ClinicalTrials.gov Identifier:
NCT05841719
Other Study ID Numbers:
  • UNISCREEN
First Posted:
May 3, 2023
Last Update Posted:
May 3, 2023
Last Verified:
Mar 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 3, 2023