ACTRN12614000944639终止未知
Effectiveness of a weight loss intervention based on diet and physical exercise to improve cognitive decision-making skills in adults with overweight and obesity compared with non-treated individuals.
School of Psychological Sciences - Monash University0 个研究点目标入组 120 人开始时间: 2014年9月3日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 终止
- 发起方
- 入组人数
- 120
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Non-randomised trial
- 主要目的
- Treatment
入排标准
- 年龄范围
- 18 Years 至 60 Years（—）
- 性别
- All
入选标准
- •Healthy weight adults: Age between 18 and 60; Body Mass Index (BMI) between 18 kg/m2 – 24.9kg/m2
- •Excess weight adults: Age between 18 and 60; Body Mass Index (BMI) between 25 kg/m2 – 40kg/m2
排除标准
- •Overweight participants who are taking part in the weight management program: (1) current or previous pregnancy (within past 6 months) or lactating; (2) history of substance
- •use (drug or alcohol); (3) history of head trauma or neurological illness impacting Central Nervous System or undergone radiation treatment; (4) current diagnosis of depression; (5) unable to read and converse in English; (6) clinically diagnosed or screen positive for disordered eating.
- •Normal-weight and overweight participants no taking part in the weight management program: (1) current or previous pregnancy (within past 6 months) or lactating; (2) current or recent history of health condition (including cancer; thyroid disease; surgery; hepatic disease; stage 3-5
- •CKD; eating disorders; those who have previously undergone radiation treatment); (3) current comorbid medical conditions associated with excess weight (e.g., type II diabetes, hypertension); (4) has undergone weight loss surgery; (5) taking weight loss drugs; (6) history of substance use (drug or alcohol); (7) history of head trauma or neurological illness impacting Central Nervous System; (8) current diagnosis of depression; (9) has lactose intolerance; (10) unable to read and converse and English; (11) clinically diagnosed or screen positive for disordered eating using.
- •Eligible overweight and obese participants are healthy volunteers. Participants will be asked to provide a finger prick blood sample in order to measure fasting plasma glucose. If a blood glucose reading greater than or equal to 7.0mmol/l is recorded which is indicative of diabetes, the participant will be referred to their GP and not able to proceed further with the study. Furthermore, blood pressure will be measured with an automated sphygmomanometer. If a blood pressure reading greater than or equal to 140/90 mm Hg is recorded which is indicative of hypertension, the participant will not be able to proceed further with the study.
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