The Effects of Nutritional Intervention on Health Parameters in Participants With Type 2 Diabetes Mellitus
- Conditions
- Type 2 Diabetes MellitusDiabetesHypertensionDiabetes Mellitus Non-insulin-dependentDiabetes Mellitus Type 2 in ObeseDiabetes Mellitus Type 2
- Interventions
- Behavioral: Nutritional Intervention
- Registration Number
- NCT06235762
- Lead Sponsor
- Sao Jose do Rio Preto Medical School
- Brief Summary
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.
- Detailed 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.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 84
Not provided
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Conventional Medical Evaluation Plus Nutritional Assessment Nutritional Intervention Participants in the intervention group will undergo the same medical care, concomitantly with nutritional assessment.
- Primary Outcome Measures
Name Time Method Body Mass Index (kg/m²). 12 months Evaluate the impact of nutritional intervention on Body Mass Index (kg/m²) between the 0th and 12th month.
glycated hemoglobin (HBA1C) rates (%) 12 months Evaluate the impact of nutritional intervention on Glycated Hemoglobin (HBA1C) (%) between the 0th and 12th month.
Triglycerides concentration (mg/dl) 12 months Evaluate the impact of nutritional intervention on Triglycerides(mg/dl) between the 0th and 12th month.
Waist circumference (cm) 12 months Evaluate the impact of nutritional intervention on Waist circumference (cm) between the 0th and 12th month.
Total Cholesterol ( TC) concentration (mg/dl) 12 months Evaluate the impact of nutritional intervention on Total Cholesterol ( TC) (mg/dl) between the 0th and 12th month.
fasting blood glucose concentration (mg/dl) 12 months Evaluate the impact of nutritional intervention on Fasting blood glucose (mg/dl) between the 0th and 12th month.
Systolic Blood Pressure (SBP) (mmHg) 12 months Evaluate the impact of nutritional intervention on Systolic Blood Pressure (SBP) (mmHg) between the 0th and 12th month.
Diastolic Blood Pressure (DBP) (mmHg) 12 months Evaluate the impact of nutritional intervention on Diastolic Blood Pressure (DBP) (mmHg) between the 0th and 12th month.
Heart Rate (HR) beats per minute (bpm) 12 months Evaluate the impact of nutritional intervention on Diastolic Blood Pressure (DBP) (mmHg) between the 0th and 12th month.
Weight (kg) 12 months Evaluate the impact of nutritional intervention on weight (kg) between the 0th and 12th month.
Waist Hip Ratio (WHR) [Waist circumference (cm)/hip circumference(cm)] 12 months Evaluate the impact of nutritional intervention on Waist Hip Ratio (WHR) between the 0th and 12th month.
LDL Cholesterol (LDL-C) concentration (mg/dl) 12 months Evaluate the impact of nutritional intervention on LDL Cholesterol (LDL-C) (mg/dl) between the 0th and 12th month.
HDL Cholesterol (HDL-C) concentration (mg/dl) 12 months Evaluate the impact of nutritional intervention on HDL Cholesterol (HDL-C)(mg/dl) between the 0th and 12th month.
- Secondary Outcome Measures
Name Time Method Sleep duration (hours) (more than 6 hours or less than 6 hours) 12 months Observe changes in sleep duration (h) between the 0th and 12th month. This qualitative variation will be measured by the standard protocol of conventional clinical nutritional analysis, using the metric of (more than 6h or less than 6h of sleep). Individuals who report "\>6" will be considered to have slept more than 6 hours per night and individuals who report "\<6" will be considered to have slept less than 6 hours per night.
Night awakenings (amount/ number) 12 months Observe changes in night awakenings between the 0th and 12th month. This qualitative variation will be measured by the standard protocol of conventional clinical nutritional analysis, using the metric of (more than 1 nighttime awakening or no nighttime awakenings). Individuals who report "\>1" will be considered to have 1 or more awakenings and individuals who report "0" will be considered to have not awakened during sleep.
Skipping breakfast (yes or no) 12 months Observe changes in breakfast skipping habits between the 0th and 12th month.This qualitative variation will be measured by the standard protocol of conventional clinical nutritional analysis, using the metric of (yes or no). Individuals who report "yes" will be considered to have skipped breakfast and individuals who report "no" will be considered to have not skipped breakfast.
Physical activity level (sedentary, moderate, advanced) 12 months Observe changes in Physical activity level between the 0th and 12th month. The presence or absence of physical exercise will be assessed through nutritional history. Patients with levels equal to or greater than 5 training sessions per week, with a total duration of 250 minutes/week, were considered very active/advanced. Patients with levels equal to or greater than 3 training sessions per week, with a total duration of 150 minutes/week, were considered active/moderate. Individuals below this recommendation were considered sedentary.
Trial Locations
- Locations (1)
Faculty of Medicine in São José do Rio Preto
🇧🇷São José do Rio Preto, São Paulo, Brazil