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The Effects of Nutritional Intervention on Health Parameters in Participants With Type 2 Diabetes Mellitus

S

Sao Jose do Rio Preto Medical School

Status

Completed

Conditions

Hypertension
Diabetes
Diabetes Mellitus Type 2 in Obese
Type 2 Diabetes Mellitus
Diabetes Mellitus Type 2
Diabetes Mellitus Non-insulin-dependent

Treatments

Behavioral: Nutritional Intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT06235762
33554520.0.0000.5415

Details and patient eligibility

About

The goal of this clinical trial is to evaluate the effects of nutritional intervention on anthropometric, biochemical and cardiovascular parameters in participants with type 2 diabetes mellitus. Participants will be distributed into 2 groups (control and intervention). Participants in the control group will only undergo conventional medical assessment and participants in the intervention group will receive the same medical care, concomitantly with nutritional assessment. The nutritional intervention is expected to reduce anthropometric data, glycemic and cardiovascular parameters in participants with T2DM, as opposed to the control group.

Full description

The goal of this clinical trial is: 1- Evaluate the effects of nutritional intervention on anthropometric parameters {Weight, Body Mass Index (BMI), Waist Circumference and Waist Hip Ratio (WHR)}, biochemical parameters {Fasting blood glucose, Glycated Hemoglobin (HBA1C), Total Cholesterol ( TC), LDL Cholesterol (LDL-C), HDL Cholesterol (HDL-C) and Triglycerides} and cardiovascular {Systolic Blood Pressure (SBP), Diastolic Blood Pressure (DBP) and Heart Rate (HR)}. 2- Evaluate behavioral patterns related to lifestyle, such as skipping breakfast, sleep quality (induction, maintenance and awakenings) and frequency of physical activity. 3-Support knowledge to the participant to build eating autonomy, consequently improving quality of life in the long term.

This research will recruit participants diagnosed with T2DM (of both sexes aged between 18 and 80 years), at the Diabetes Outpatient Clinic and Hypertension at the Faculty of Medicine of São José do Rio Preto. The interventions will be distributed in quarterly meetings. Participants will be randomly distributed into 2 groups (control and the intervention group). The 40 participants in the control group will only undergo conventional medical evaluation and the 40 Participants in the intervention group will undergo the same medical care, concomitantly with nutritional assessment. Nutritional services will be made up of: A) Application of protocols (1-Nutritional History - Anthropometric, Biochemical and Clinical; 2-Habitual Food Record; 3-Sociodemographic protocol); B) Delivery of nutritional guidelines; C) Preparation of an individualized eating plan (inspired by the Mediterranean Diet and DASH diet with moderate carbohydrate content and restriction of saturated fats).

It is expected that interventions modulate the recovery of nutritional status, dietary inadequacies, parameters anthropometric, biochemical, cardiovascular and clinics, thus improving quality of life and reducing the risk of events in participants with T2DM in long term. In this way, the participants in treatment with nutritional support will be able to achieve greater benefit, maximizing the construction of a process of autonomy to feed.

Enrollment

84 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

  • Inclusion criteria - Participants with:

    • Age: Adults above 18 years to below 80 years.
    • Diagnosis of the disease: T2DM, that is, fasting blood glucose values equal to or greater than 126 mg/dL and glycated hemoglobin equal to or greater than 6.5%.
    • Gender: Male and female
    • Availability to participate in quarterly meetings during a period of 36 months.
    • Nutritional status: initial diagnosis of overweight or obesity, that is, with BMI above 24.9kg/m².
    • Sedentary.
  • Exclusion criteria - Participants who:

    • They had difficulties answering the requested instruments.
    • They demonstrated impediments to assiduity in data collection.
    • They did not present a diagnosis of T2DM.
    • They were using insulin therapy.
    • They were using SGLT-2 inhibitors and/or GLP-1 analogues.
    • People with Chronic Kidney Disease.
    • Eutrophic or malnourished.
    • Physical exercisers, that is, more than 150 minutes of moderate to intense exercise per week.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

84 participants in 2 patient groups

Conventional Medical Evaluation
No Intervention group
Description:
Participants in the control group will only undergo conventional medical evaluation.
Conventional Medical Evaluation Plus Nutritional Assessment
Active Comparator group
Description:
Participants in the intervention group will undergo the same medical care, concomitantly with nutritional assessment.
Treatment:
Behavioral: Nutritional Intervention

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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