- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT03164499
Intensive Intervention to Improve Lifestyles in Subjects With Intermediate Cardiovascular Risk.
Effectiveness of an Intensive Intervention to Improve Lifestyles in Subjects With Intermediate Cardiovascular Risk: a Randomized Controlled Trial.
연구 개요
상태
정황
연구 유형
등록 (실제)
단계
- 해당 없음
연락처 및 위치
연구 장소
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Castilla And Leon
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Salamanca, Castilla And Leon, 스페인, 37003
- Primary Care Research Unit, The Alamedilla Health Center
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
- Adults aged 35-74 years who had an intermediate cardiovascular risk defined according to the Framingham risk equation will be included.
Exclusion Criteria:
- Personal history of atherosclerotic disease.
- Unable to do exercise or follow the Mediterranean diet.
- Institutionalized.
- Terminal illness.
- Mental disorders that limited the intervention compliance.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 방지
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 하나의
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
활성 비교기: Control group
Individual counselling on lifestyles.
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Individual standardized counselling on healthy diet, daily physical activity, stress management, smoking cessation, and moderation in alcohol consumption.
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실험적: Intervention group
Individual counselling on lifestyles and additional group counselling on lifestyles.
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Individual standardized counselling on healthy diet, daily physical activity, stress management, smoking cessation, and moderation in alcohol consumption.
Group sessions focusing on cardiovascular risk, diet and moderation in alcohol consumption, physical activity and stress management, and smoking cessation will be held in health centres for four consecutive weeks. Each session will last 60-90 minutes, and will be led by two trained nurse practitioners. Ten participants will assist each group. During each session, attendance will be recorded and printed educational materials related to the topic addressed will be distributed. Follow-up calls to reinforce lifestyle modification and record the barriers to behaviour change found will be performed 6 and 9 months after enrolment. |
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Adherence to the Mediterranean diet
기간: 1 year
|
Measurement by validated 14-point Mediterranean Diet Adherence Screener
|
1 year
|
|
Self-reported physical activity
기간: 1 year
|
Measurement by short version of the International Physical Activity Questionnaire
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1 year
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Changes in physical activity
기간: 1 year
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Measurement by Pedometer
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1 year
|
|
Changes in dietary pattern
기간: 1 year
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Measurement by semi-quantitative Food Frequency Questionnaire
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1 year
|
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Cardiovascular risk factors
기간: 1 year
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Measurement by Framingham Risk Score
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1 year
|
|
Body composition
기간: 1 year
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Measurement by Bioelectrical Impedance Analyzer
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1 year
|
|
Cardio-ankle vascular index (CAVI)
기간: 1 year
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Measurement by Vasera® VS-2000 device
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1 year
|
|
Brachial-ankle pulse wave velocity (ba-PWV)
기간: 1 year
|
Measurement by Vasera® VS-2000 device
|
1 year
|
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Ankle-brachial index (ABI)
기간: 1 year
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Measurement by Vasera® VS-2000 device
|
1 year
|
|
Health related quality of life
기간: 1 year
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Measurement by Spanish version of the SF-12 questionnaire
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1 year
|
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Immediate verbal memory
기간: 1 year
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Assessment by immediate recall of a list of 15 words, in three attempts
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1 year
|
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Delayed verbal memory
기간: 1 year
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Assessment by free recall of the words learnt in the first part of the study after a period of approximately 10 minutes
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1 year
|
|
Phonological fluency
기간: 1 year
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Assessment by enumerating for one minute as many words as possible starting with different letters
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1 year
|
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Attention
기간: 1 year
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Assessment by Trail Making Test A
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1 year
|
|
Processing speed
기간: 1 year
|
Assessment by Trail Making Test B
|
1 year
|
|
Executive functions
기간: 1 year
|
Assessment by Trail Making Test B
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1 year
|
|
Working memory
기간: 1 year
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Assessment by WAIS Digit Span Backward test
|
1 year
|
|
Sustained attention
기간: 1 year
|
Assessment by Stroop test
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1 year
|
|
Selective attention
기간: 1 year
|
Assessment by Stroop test
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1 year
|
공동 작업자 및 조사자
수사관
- 수석 연구원: Sara Mora Simón, PhD, Primary Care Research Unit, The Alamedilla Health Center
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (실제)
연구 완료 (실제)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
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. .
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