- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT04632823
"The Effect of Comprehensive Non-pharmacological Treatment on Metabolic Disorders in Type 2 Diabetic Patients"
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Patients in the intervention group will participate in a comprehensive non-pharmacological treatment of type 2 diabetes, the main components are:
- changing the meal plan (individual and group counseling, assistance in developing menus and determining the calorie intake, keeping a food diary)
- individually dosed physical exercises using specific exercise program;
- comprehensive training (course of interactive lessons, self-control training). The program included group sessions with a team of specialists: nutritionist, endocrinologist, physical therapy doctor and included 3 sessions per week for 24 weeks. Each visit included teaching patients in a group format and in an interactive form (classes with specialists alternated), performing physical exercises using the specific exercise program under the supervision of a physiotherapy physician, evaluating medical indicators, and a self-control diary.
Patients in the control group will not participate in group sessions, but they had the opportunity to receive non-pharmacological care provided in the framework of free outpatient care. Their indicators will be recorded during a routine visit to the doctor at the baseline, after 12 and 24 weeks.
Undersøgelsestype
Tilmelding (Forventet)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
-
-
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Moscow, Den Russiske Føderation, 101000
- Aktiv, ikke rekrutterende
- National Medical Research Center for Endocrinology, Ministry of Health of the Russian Federation
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-
-
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Astana, Kasakhstan, 010000
- Rekruttering
- Astana Medical University
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Kontakt:
- Yerbolat Dalenov, Professor
- Telefonnummer: +77017694241
- E-mail: dalenov.e@amu.kz
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Underforsker:
- Anna Bazarova, Docent
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Astana, Kasakhstan, 010000
- Rekruttering
- The Center for Preventive Medicine and Life Extension of Nur-Sultan
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Kontakt:
- Viktoriya Li, PhD
- Telefonnummer: +77785568055
- E-mail: liviktoriya0509@gmail.com
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Aktobe Region
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Aktobe, Aktobe Region, Kasakhstan, 030000
- Aktiv, ikke rekrutterende
- West Kazakhstan Marat Ospanov Medical University
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- medically diagnosed with type 2 diabetes mellitus
- HbA1c result of ≤7.0% within the past 2 months
- body mass index (BMI) of ≥26 kg/m^2
- hypoglycemic therapy: metformin only
Exclusion Criteria:
- pregnancy
- the use of other hypoglycemic drugs
- the use of medication for weight loss
- cardiovascular diseases (heart attack or cardiac procedure within the past 3 months)
- had stroke or history of treatment for transient ischemic attacks in the past 3 months
- had chronic renal failure or were on dialysis
- any conditions that do not allow the patient to perform the complex of the proposed physical exercises
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Enkelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Comprehensive non-pharmacological program intervention
The experimental group receives usual diabetes care plus 24 weeks of the comprehensive non-pharmacological program intervention.
|
dietary supplement, specific type of exercise, self-management education
|
|
Ingen indgriben: Usual diabetes care
This group is control, the patients receive usual diabetes care routines.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Change from Baseline Glycosylated Hemoglobin at 6 months
Tidsramme: at baseline and at 24-week postrandomization
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HbA1c value
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at baseline and at 24-week postrandomization
|
|
Change from Baseline Body Mass Index at 6 months
Tidsramme: at baseline and at 24-week postrandomization
|
BMI
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at baseline and at 24-week postrandomization
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Change from Baseline Blood Pressure at 6 months
Tidsramme: at baseline and at 24-week postrandomization
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Systolic and diastolic blood pressure at the brachial artery
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at baseline and at 24-week postrandomization
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Change from Baseline Lipid Profiles at 6 months
Tidsramme: at baseline and at 24-week postrandomization
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Total Triglyceride, Total Cholesterol, high-density lipoprotein (HDL), and low-density lipoprotein (LDL)
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at baseline and at 24-week postrandomization
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Change from Baseline Homeostasis ModelAssessment of Insulin Resistance at 6 months (HOMA-IR)
Tidsramme: at baseline and at 24-week postrandomization
|
Homeostasis ModelAssessment of Insulin Resistance
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at baseline and at 24-week postrandomization
|
Samarbejdspartnere og efterforskere
Sponsor
Efterforskere
- Ledende efterforsker: Viktoriya Li, PhD, Astana Medical University
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Forventet)
Studieafslutning (Forventet)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- AstanaMU-1
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
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