Qatar Universal Diabetes Outcomes (QUDOS) Study

Cornell University

Status: Terminated

Conditions: Type 2 Diabetes Mellitus; Diabetes Mellitus

Study type: Observational

Funder types: Other; Industry

Identifiers

NCT02660476

JIRB: 14-0032. MRC: #14461/14

Details and patient eligibility

About

QUDOS is a cross-sectional population study aiming to answer key questions about diabetes and its complications in Qatar as well as identify factors associated with the development and progression of diabetes complications.

Full description

QUDOS aims to gain a better understanding of diabetes in primary and secondary care over a period of 24 months.

A range of patients with diabetes will be sampled (including those with Type 1 diabetes as this group is under-studied in Qatar). This will be important in designing appropriate intervention plans that will improve diabetic patients' health conditions to prevent or delay the onset of complications and will provide a strong foundation for longitudinal study.

The broad objectives of the study are:

QUDOS 1: Aims to recruit 1,700 diabetic patients (including 200 with type 1 diabetes mellitus (independent of healthcare setting)) attending the hospitals and primary care and to collect the following data:

• Demographics: age, sex, ethnicity, socio-economic background, smoking status;
• Anthropometrics: vital signs, height, weight, body fat percentage, fat mass, neck and waist circumference;
• Medical History: medications, complications, comorbidities, latest HbA1c and lipid profiles and family medical history;
• Routine laboratory data;
• Lifestyle: diet, physical activity,;
• Sleep: quality and daytime sleepiness;
• Cognition and Mental Health: depression, anxiety, stress and memory;
• Diabetes microvascular complications: diabetic neuropathy, urine albumin/creatinine ratio; routine retinal screening data.
• Gut microbiome from a stool sample

QUDOS 2: To further characterise 500 patients, from the total 1500 patients with T2DM recruited in QUDOS 1, who accept to continue with QUDOS 2 (a more detailed study and assessment).

This phase aims to concentrate on the following aspects:

• Obstructive sleep apnoea;
• Sleep duration and quality;
• Diet;
• Objective physical activity;
• Stress;
• Quality of Life;
• Depression and anxiety;
• Perceived control of health;
• Detailed neuropathy screening;
• Cardiovascular function;
• Cognitive function;
• Biological samples.

Enrollment: 475 patients

Sex: All

Ages: 18 to 70 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Type 1 and Type 2 diabetes mellitus;
2. Male or Female;
3. Resident in Qatar;
4. MENA birthplace and family origin;
5. 18-70 years old;
6. Capable to give informed consent and complete the study.

Exclusion criteria

1. Known pregnancy or planning pregnancy during the duration of study; 2. Congenital disorders; 3. Terminal illness; 4. Enrolled in a clinical trial involving medication; 5. Uncontrolled mental illness preventing participation; 6. Those who have already experienced a definitive microvascular complication:

i. End-stage renal disease; ii. Major amputation; iii. Blindness.

Trial design

475 participants in 2 patient groups

QUDOS 1

Description:

Aims to recruit 1,700 diabetic patients (including 200 with type 1 diabetes mellitus (independent of healthcare setting)) attending the hospitals and primary care

QUDOS 2

Description:

To further characterise 500 patients, from the total 1500 patients with T2DM recruited in QUDOS 1, who accept to continue with QUDOS 2 (a more detailed study and assessment).