- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT01597154
Lifestyle Therapy for Youth With Type 2 Diabetes (BDT)
Beating Diabetes Together: A Randomized Controlled Trial for Intensive Lifestyle Therapy for Youth With Type 2 Diabetes
Background: Little is known about the efficacy of intensive lifestyle therapy (i.e. increased physical activity and dietary changes) for the management of glycemia and cardiometabolic risk factors in children and adolescents with type 2 diabetes (T2DM).
Our hypothesis is that education regarding healthy lifestyle changes will significantly reduce blood sugars in youth with T2DM that do not require insulin therapy. Our secondary hypothesis is that the intensive lifestyle therapy will cause quick and sustained reductions in health risk measured by body mass index (BMI), blood pressure, waist circumference, LDL cholesterol, serum triglycerides and apolipoprotein B.
연구 개요
상세 설명
연구 유형
등록 (실제)
단계
- 해당 없음
연락처 및 위치
연구 장소
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Manitoba
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Winnipeg, Manitoba, 캐나다, R3E 0P4
- Manitoba Institute of Child Health
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
- youth with a BMI considered overweight according to the International Obesity Task Force
- diagnosed with type 2 diabetes, confirmed with a 2-hour oral glucose tolerance test within two years of enrollment
Exclusion Criteria:
- youth with type 1 diabetes
- use of insulin or other anti-diabetic drugs
- youth with medication-induced diabetes
- youth who have recently been admitted to hospital with ketoacidosis
- youth have experienced weight loss or enrolled in a weightloss program in the last 6 months
- youth with an orthapaedic injury preventing them from exercising
- youth who have a history of alcohol or drug abuse
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 방지
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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실험적: Lifestyle counselling
Exercise, nutrition and self-efficacy based lifestyle training in a peer mentoring setting
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Participants will take part in 2-3 group based peer-led sessions per week in which they will learn about healthy lifestyle choices
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간섭 없음: Control
Youth randomized to the control group will receive standard care for the first 16 weeks followed by 16 weeks of intervention
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
기간 |
|---|---|
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Glycemic control determined by a standard fasting measure of glycosylated hemoglobin using internationally recognized DCCT assay
기간: 16 weeks
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16 weeks
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Cardiometabolic risk Z score
기간: 16 weeks
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This is a composite score based on BMI z-score, waist circumference, c-reactive protein (CRP), fibrinogen, low density lipoprotein (LDL) and high density lipoprotein (HDL) cholesterol, triglycerides (TG) and apolipoprotein B (apoB), and a marker of fatty liver disease, alanine transaminase (ALT)
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16 weeks
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Presence of microalbuminuria
기간: 16 weeks
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defined as a first morning albumin:creatinine ratio (ACR) 2.5-25 mg/mmol in a first morning urine collection
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16 weeks
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Hypertension
기간: 16 weeks
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defined as a systolic blood pressure load >25% or a mean 24 hour systolic blood pressure >95th %ile for sex and height on 24 hour ambulatory blood pressure monitoring
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16 weeks
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Anthropometrics
기간: 16 weeks
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Waist circumference in centimeters, body mass index (BMI) z-score and percent body fat will be assessed to determine if changes in body composition are associated with improvements in cardiometabolic risk
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16 weeks
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Cardiovascular structure and function
기간: 16 weeks
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Vascular health will be assessed with non-invasive assessments of arterial stiffness, endothelium-dependant relaxation and carotid intima media thickness which will be treated as continuous variables.
Left ventricular structure and function will be assessed using standard M-mode and doppler ultrasound techniques
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16 weeks
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공동 작업자 및 조사자
수사관
- 수석 연구원: Jonathon McGavock, PhD, University of Manitoba
연구 기록 날짜
연구 주요 날짜
연구 시작
기본 완료 (실제)
연구 완료 (실제)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (추정)
연구 기록 업데이트
마지막 업데이트 게시됨 (추정)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .