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Intensive Self-care on Glycemic Control in Outpatients With Type 2 Diabetes Mellitus: The Diabetes Care (D-CARE) Study

Educação em saúde Intensiva na atenção primária à saúde em Pacientes Com Diabetes Mellitus Tipo 2: um Ensaio clínico Randomizado - The Diabetes Care (D-CARE) Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05969015
Acronym
D-CARE
Enrollment
174
Registered
2023-08-01
Start date
2022-01-15
Completion date
2024-05-07
Last updated
2024-05-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Diseases, Diabetes Mellitus, Diabetes Mellitus, Type 2

Keywords

Self Management, Behavior, Type 2 Diabetes Mellitus, Cardiovascular Disease

Brief summary

Type 2 diabetes mellitus (T2DM) leads to a high burden of morbidity and mortality, usually attributable to cardiovascular (CVD) causes. A major concern about the disease is that the success of the treatment is highly dependent on self-management, which very often incurs the necessity of behavior change. However, modifying such behaviors, usually linked to daily-life activities, is challenging. Then, the investigators aimed to test the optimal self-management that could be achieved in a reasonable manner carried forward through the Prochaska and DiClemente behavior-changing strategy in a follow-up of 18 months, compared to usual care. Our primary outcome is the between-group difference in HbA1c (%) levels.

Interventions

BEHAVIORALProchaska and DiClemente transtheorical model

The Prochaska and DiClemente model will be combined to a self-management program in patients with T2DM within 18 months. They will be classified accordingly to their readiness for changing. A care provider will manage the group towards an optimal self-management, aiming to improve their glycemic control and other outcomes of relevance. We will conduct 1 session per week until the end of 12nd intervention month. After, the sections will be conducted each 2 weeks until the end of the trial. Healthcare professional will provide support to the care provider. The recommended processes to progress the patients will be used to trigger them accordingly to their stage, at the discretion of the care provider. We will also consider individualities and non-anticipated problems as a part of the process of behavior changing.

Sponsors

Prefeitura Municipal de Criciúma
CollaboratorUNKNOWN
Conselho Nacional de Desenvolvimento Científico e Tecnológico
CollaboratorOTHER_GOV
Departamento de Promoção da Saúde (DEPROS), Secretaria de Atenção Primária à Saúde (SAPS)
CollaboratorUNKNOWN
Hospital Universitário São José
CollaboratorOTHER
Universidade do Extremo Sul Catarinense - Unidade Academica de Ciecias da Saude
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

Outcomes' assessors will be masked to assigned interventions in all measurements they would perform.

Intervention model description

This is an effectiveness/pragmatic, parallel-arm, randomized, superiority trial.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Outpatients diagnosed with type 2 diabetes mellitus - T2DM (HbA1c % - ≥ 6.5%, or taking at least one oral hypoglycaemic agent, or medical diagnosis); * To be regularly assisted by the Sistema Único de Saúde and to have been saw at least one year before randomization; * Readiness for behavior-changing within the pre-action stages: pre-contemplation, contemplation and preparation; * T2DM patient of challenging handling (e.g., frequent hypoglycaemic seizures, cardiovascular disease (CVD), etc.);

Exclusion criteria

* Pregnant women; * People living with HIV/AIDS; * T2DM patients taking erythropoietin, recent blood loss, recent blood transfusion and severe anaemia; * T2DM patients with CVD under non-optimized treatment; or those that made any CVD procedure; or CVD event (e.g., myocardial infarction) within three months before randomization; * T2DM patients with severe eye and retine disease; * Patients participating in another study simultaneously; * Patients living with others in the same place.

Design outcomes

Primary

MeasureTime frameDescription
Glycemic controlat 3-monthly intervals during 18 monthGlycemic control as measured by glycated haemoglobin (HbA1c) levels (%)

Secondary

MeasureTime frameDescription
Blood Pressure controlat 6-monthly intervals during 18 monthBlood Pressure control as measured by office systolic and diastolic blood pressure (SBP/DBP in mmHg)
All-cause number of health care settings visitsat 6-monthly intervals during 18 monthAll-cause number of health care settings visits measured by counts
Attributable number of health care settings visits to type 2 diabetes mellitusat 6-monthly intervals during 18 monthAttributable number of health care settings visits to type 2 diabetes mellitus measured by counts
Weightat 6-monthly intervals during 18 monthAnthropometric variables measured in kg
Heightat 6-monthly intervals during 18 monthAnthropometric variables -measured in meters
Body mass indexat 6-monthly intervals during 18 monthAnthropometric variables - kg per square meter
Abdominal circumferenceat 6-monthly intervals during 18 monthAnthropometric variables - measured in centimeters (cm)
Physical activity levels - Guidelines for Data Processing and Analysis of the International Physical Activity Questionnaire (IPAQ) - Short Format 6-monthly intervals during 18 monthThere are three levels of physical activity suggested for classifying populations; these are the new proposed levels, which take account of the concept of total physical activity of all domains. The proposed levels are: inactive; minimally active and HEPA activeí health-enhancing physical activity; a highly active category
Depression scores by Hamilton Depression Rating Scale - HDR-Sat 6-monthly intervals during 18 monthA score of 0-7 is generally accepted to be within the normal range (or in clinical emission), while a score of 20 or higher (indicating at least moderate severity) is usually required for entry into a clinical trial.
MARKERS OF FOOD CONSUMPTION - Food and nutrition surveillance system - Brazilat 6-monthly intervals during 18 monthQualitative assessment of food intake for the previous day.
Number of hypoglycemiants, anti-hypertensives and hypolipidemic drugsat 6-monthly intervals during 18 monthCount of hypoglycemiants, anti-hypertensives and hypolipidemic drugs taken by patients
Low density lipoprotein levels - LDL-Cat 3-monthly intervals during 18 monthSerum LDL-C levels in mg/dL
High density lipoprotein levels - HDL-Cat 3-monthly intervals during 18 monthSerum HDL-C levels in mg/dL
Total cholesterol levels - TCat 3-monthly intervals during 18 monthSerum TC levels in mg/dL
Total triglycerides levels - TGat 3-monthly intervals during 18 monthSerum TG levels in mg/dL
Creatinine levelsat 3-monthly intervals during 18 monthSerum creatinine levels in mg/dL
Diabetes Mellitus knowledge (DKN-A)at 6-monthly intervals during 18 monthThe measuring scale used is from 0 to 15. A score of one (1) is attributed to the correct answer and of zero (0) for the incorrect answer. A score higher than eight (8) indicates knowledge about diabetes mellitus
Diabetes Attitude Questionnaire (ATT-19)at 6-monthly intervals during 18 monthATT-19 is an instrument that seeks to measure psychological adjustment for diabetes mellitus, developed in response to the need for evaluation of the psychological and emotional aspects of the disease. It contains nineteen items that include six factors: a) DM-associated stress, b) treatment receptivity, c) trust in the treatment, d) personal efficiency, e) health perception, and f) social acceptance, with the answers measured using a five-point Likert scale (completely disagree - score 1; up to completely agree - score 5). The total value of the score can vary from 19 to 95 points. A score higher than 70 indicates a positive attitude toward the disease. In this instrument, attitude is related to the decision of the individual to adopt or not the self-care measures for diabetes control.
Anxiety scores - Hamilton Anxiety Rating Scale (HAM-A)at 6-monthly intervals during 18 monthEach item is scored on a scale of 0 (not present) to 4 (severe), with a total score range of 0-56, where \<17 indicates mild severity, 18-24 mild to moderate severity and 25-30 moderate to severe.

Other

MeasureTime frameDescription
Adverse Eventsat 6-monthly intervals during 18 monthAdverse Events as counts: all-cause mortality, cardiovascular mortality, STEMI and non-STEMI (fatal and non-fatal), heart failure diagnosis, unstable angina hospitalizations, cardiovascular procedures, hospital admission or re-admission, chronic kidney disease, retinopathy diagnosis, falls.

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026