Study About Adherence and Tolerance of an Oral Nutritional Supplement (ONS) Specific for Diabetic Patient. (DIABEST)

Instituto de Investigación Hospital Universitario La Paz

Status

Unknown

Conditions

Diabetes

Malnutrition

Treatments

Dietary Supplement: FontActiv DiaBest HP/HC

Study type

Observational

Funder types

Other

Identifiers

NCT05488210

PI-6092

Details and patient eligibility

About

Diabetes Mellitus (DM) is one of the most prevalent chronic diseases today, it is reaching epidemic proportions, mainly caused by the increase in type 2 diabetes (DM2).The foundation of any hypoglycemic treatment is based on a healthy diet, daily physical exercise and adequate health education with the collaboration of the patient. Diet is sometimes the only necessary therapy since approximately 80% of patients with DM2 are usually overweight, what is mainly wanted with diet is to achieve normal blood glucose levels both fasting and in the postprandial phase. This diet must be a varied diet combining foods from the different food groups; however, carbohydrate control must be one of the key strategies for glycemic control. Currently, there is also talk of the concept of disease-related malnutrition (DRM). DRM is malnutrition associated with a pathological state, with the presence of inflammation being a key factor in determining its etiology. This inflammation can be chronic or acute depending on the type of pathology. Therefore, the fiber and carbohydrate composition of oral nutritional supplements are important for glycemic control, so a study is proposed to evaluate the effect of consuming a ONS hypercaloric/high-protein (HC/HP) with fiber, and enriched in calcium, Vitamin D and DHA on adherence and tolerance of the product and nutritional status in patients with DM2 and malnutrition.

Full description

Longitudinal, prospective exploratory study, to evaluate the effect of consuming an oral nutritional supplement (ONS) HC/HP with fiber, and enriched in calcium, Vitamin D and Docosahexaenoic acid (DHA) on adherence and tolerance of the product and nutritional status in patients with DM2 and malnutrition, in a period of 60 days. Twenty-four volunteers will be recruited at the La Paz University Hospital of Madrid. Participants should meet the next inclusion criteria: men and woman enter 18 and 85, with DM2 previously diagnosed and controlled, with malnutrition diagnosed according to the Global Leadership Initiative on Malnutrition (GLIM) criteria, who require taking ONS, willing to consume the ONS during the study and adequate cultural level and understanding of the clinical study. Follow up will include 4 individualized visits.

Enrollment

24 estimated patients

Sex

All

Ages

18 to 85 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Men and women enter 18 and 85 years old.
Patients with DM2 previously diagnosed and controlled.
Patients with malnutrition diagnosed according to GLIM criteria.
Patients who require taking ONS.
Patients willing to consume the ONS during the study period.
Patients with adequate cultural level and understanding of the clinical study.
Patients who agree to voluntarily participate in the study and who give their informed consent in writing.

Exclusion criteria

Subjects with enteral or parenteral nutrition.
Subjects with poorly controlled DM2.
Subjects with dementia, eating behavior disorders, history of serious neurological or psychiatric pathology that may interfere with adherence to the consumption of the ONS.
Subjects suffering from alcoholism or substance abuse that may interfere with adherence to the consumption of the ONS.
Subjects with a diagnosis of kidney or liver disease under pharmacological treatment.
Subjects with infections or any condition that interferes with nutrient digestion, absorption, metabolism, or excretion (including gastroparesis).
Subjects with chronic gastrointestinal diseases that affect the digestion or absorption of nutrients.
Subjects with allergies or intolerances to any of the ingredients of the formula.
Subjects with socio-family problems that prevent them from participating in the study.
Pregnant or lactating women.