跳至主要内容
临床试验/NCT00716027
NCT00716027已完成不适用

Applying Social Comparison Theory to Behavioral Weight Loss: Does Modifying Group Membership Improve Outcome?

The Miriam Hospital1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2008年7月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
80
试验地点
1
主要终点
weight

研究概览

简要总结

The purpose of this study is to determine whether a modified behavioral treatment for weight loss that includes one-on-one treatment for individuals struggling to lose weight is associated with more weight loss than a standard behavioral treatment.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
21 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •BMI between 27 and 45 kg/m2

排除标准

  • •participating in a weight loss program or taking a weight loss medication
  • •currently pregnant, lactating, or less than 6-months post-partum or plan to become pregnant during the time of the intervention.
  • •report a heart condition, chest pain during periods of activity or rest, or loss of consciousness
  • •report conditions that would render the participant unlikely to follow the study protocol (e.g., terminal illness, relocation, substance abuse, sever psychiatric condition, dementia).

研究组 & 干预措施

1

Active Comparator

A 24-week intervention in which individuals will meet weekly to be instructed on behavioral change associated with weight loss, including modifying dietary intake, self-monitoring weight and eating behaviors, and increasing physical activity.

干预措施: Standard behavioral treatment for weight loss (Behavioral)

2

Experimental

A 24-week intervention in which individuals will meet weekly to be instructed on behavioral change associated with weight loss, including modifying dietary intake, self-monitoring weight and eating behaviors, and increasing physical activity. In this intervention, individuals not meeting weight loss goals will be given one-on-one treatment.

干预措施: Modified behavioral treatment for weight loss (Behavioral)

结局指标

主要结局

weight

时间窗: weekly for 24-weeks

次要结局

未报告次要终点

研究者

申办方类型
Other

研究点 (1)

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