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临床试验/NCT04400253
NCT04400253已完成不适用

A Multilevel Physical Activity Intervention for South Asian Women and Girls (SAATH)

Northwestern University2 个研究点 分布在 1 个国家目标入组 252 人开始时间: 2020年8月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
252
试验地点
2
主要终点
Averaged daily minutes spent in moderate- and vigorous-intensity physical activity measured by ActiGraph accelerometers

研究概览

简要总结

South Asian immigrant women and girls are at increased risk for insufficient physical activity and are not being reached by current approaches to physical activity promotion. This randomized control trial study will test the effectiveness and implementation of a multi component physical activity intervention directed at the environment, family, interpersonal and individual levels to promote physical activity among South Asian immigrant mothers and daughters.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Investigator)

入排标准

年龄范围
11 Years 至 —(Child, Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • 未提供

排除标准

  • having known medical condition that restricts ability to participate in moderate intensity Physical Activity
  • Unable to complete study procedures (including not wearing accelerometer during run-in)
  • Currently pregnant
  • Unable to provide informed consent or assent.

结局指标

主要结局

Averaged daily minutes spent in moderate- and vigorous-intensity physical activity measured by ActiGraph accelerometers

时间窗: The outcome will be assessed before the intervention (week 0) and after the intervention (week 18)

Moderate- and vigorous-intensity physical activity will be identified based on the accelerometer count cut-point for moderate intensity and daily minutes spent in moderate- and vigorous-intensity physical activity estimated for seven days will be averaged

次要结局

  • Averaged daily minutes spent in walking or running behavior measured by ActiGraph accelerometers(The outcome will be assessed before the intervention (week 0) and after the intervention (week 18))
  • Self-efficacy score measured by Dishman's Barriers to Self-Efficacy questionnaire(The outcome will be assessed before the intervention (week 0) and after the intervention (week 18))
  • Averaged daily hours spent in sedentary behaviors measured by ActiGraph accelerometers(The outcome will be assessed before the intervention (week 0) and after the intervention (week 18))
  • Systolic and diastolic blood pressure (mmHg) measured by a sphygmomanometer(The outcome will be assessed before the intervention (week 0) and after the intervention (week 18))
  • Self-efficacy score measured by the Exercise Confidence Survey(The outcome will be assessed before the intervention (week 0) and after the intervention (week 18))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Namratha Kandula

Prinicipal Investigator

Northwestern University

研究点 (2)

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