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临床试验/NCT03601663
NCT03601663已完成不适用

Exploring the Effect of an eHealth Intervention on Women's Physical Activity Behaviour

University of Ottawa1 个研究点 分布在 1 个国家目标入组 49 人开始时间: 2018年9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
49
试验地点
1
主要终点
Physical activity behaviour: Custom strength and resistance training questionnaire

研究概览

简要总结

Physical activity has been shown to reduce the risk of chronic diseases and promote physical and mental health and wellbeing, yet few women are active enough to see these benefits. Wearable activity trackers show promise for helping people increase their physical activity levels by supporting self-monitoring. However, few researchers have examined how providing people with these devices impacts physical activity levels, or motivation for physical activity which is a significant and robust predictor of physical activity. Based on previous research, it is possible that women's physical activity levels would be more likely to increase if they received an autonomy-supportive intervention to enhance motivation in addition to a wearable activity tracker. A pilot, three-armed randomized controlled trial was developed to test this hypothesis and to assess if changes in perceived autonomy-support, basic psychological need satisfaction/thwarting, motivational regulations, wellbeing indicators are associated with changes in physical activity over time.

研究设计

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

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
Female
接受健康志愿者
是

入选标准

  • •to participate in the intervention:
  • •Are a woman between the ages of 18 and 65 years
  • •Can understand, read, and speak in English
  • •Are able to safely engage in physical activity
  • •Are not currently pregnant or lactating
  • •Currently participating in less than 150 minutes of moderate or vigorous intensity physical activity and less than two strength training sessions per week
  • •Are overweight or obese (i.e., have a body mass index greater than 25kg/m2)
  • •Have access to the Internet and an email account
  • •Have not used a wearable activity tracker within the past year (e.g., Fitbit, Apple Watch, Garmin, Polar)
  • •Live within 50km of the University of Ottawa

排除标准

  • 未提供

研究组 & 干预措施

Group 1

Experimental

Participants in the main experimental group will receive a copy of the Canadian Physical Activity Guidelines that provide basic information about and recommendations for physical activity, a wearable activity tracker to support self-monitoring, and autonomy-support delivered through weekly emails to help enhance motivation for physical activity.

干预措施: Physical Activity Information (Behavioral)

Group 1

Experimental

Participants in the main experimental group will receive a copy of the Canadian Physical Activity Guidelines that provide basic information about and recommendations for physical activity, a wearable activity tracker to support self-monitoring, and autonomy-support delivered through weekly emails to help enhance motivation for physical activity.

干预措施: Physical Activity Monitoring (Behavioral)

Group 1

Experimental

Participants in the main experimental group will receive a copy of the Canadian Physical Activity Guidelines that provide basic information about and recommendations for physical activity, a wearable activity tracker to support self-monitoring, and autonomy-support delivered through weekly emails to help enhance motivation for physical activity.

干预措施: Autonomy-support (Behavioral)

Group 2

Active Comparator

Participants in this comparison group will receive a copy of the Canadian Physical Activity Guidelines that provide basic information about and recommendations for physical activity, and a wearable activity tracker to support self-monitoring. They will not receive any specific support to enhance motivation for physical activity.

干预措施: Physical Activity Information (Behavioral)

Group 2

Active Comparator

Participants in this comparison group will receive a copy of the Canadian Physical Activity Guidelines that provide basic information about and recommendations for physical activity, and a wearable activity tracker to support self-monitoring. They will not receive any specific support to enhance motivation for physical activity.

干预措施: Physical Activity Monitoring (Behavioral)

Group 3

Active Comparator

Participants in this information-only comparison group will receive a copy of the Canadian Physical Activity Guidelines that provide basic information about and recommendations for physical activity.

干预措施: Physical Activity Information (Behavioral)

结局指标

主要结局

Physical activity behaviour: Custom strength and resistance training questionnaire

时间窗: Baseline (week 0), post-intervention (week 9), and follow-up (week 21).

Change in strength and resistance training habits from baseline to post-intervention, and from post-intervention to follow-up.

Physical activity behaviour: International Physical Activity Questionnaire Short Form (IPAQ-S)

时间窗: Baseline (week 0), post-intervention (week 9), and follow-up (week 21).

Change in self-reported physical activity (over the past 7 days) from baseline to post-intervention, and from post-intervention to follow-up.

次要结局

  • Physical activity behaviour: Direct measure(Duration of intervention phase (8 weeks).)
  • Perceived autonomy support: Perceived Autonomy Support Scale for Exercise Settings (PASSES; Hagger et al., 2007)(Baseline (week 0), post-intervention (week 9), and follow-up (week 21).)
  • Basic psychological need thwarting: Psychological Need Thwarting Scale (PNTS; Bartholomew, Ntoumanis, Ryan, & Thøgersen-Ntoumani, 2011)(Baseline (week 0), post-intervention (week 9), and follow-up (week 21).)
  • Positive and Negative Affect Schedule (I-PANAS-SF; Thompson, 2016; Watson, Clark, & Tellegen, 1988).(: Baseline (week 0), post-intervention (week 9), and follow-up (week 21).)
  • Wearable activity tracker usage: Multiple choice questions(Post-intervention (week 9).)
  • Basic psychological need satisfaction: Psychological Need Satisfaction in Exercise Scale (PNSE; Wilson, Rogers, Rodgers, & Wild, 2006)(Baseline (week 0), post-intervention (week 9), and follow-up (week 21).)
  • Vitality: Subjective Vitality Scale (Ryan & Frederick, 1997).(Baseline (week 0), post-intervention (week 9), and follow-up (week 21).)
  • Depression: Patient Health Questionnaire (PHQ-9; Kroenke, Spitzer, & Williams, 2001).(Baseline (week 0), post-intervention (week 9), and follow-up (week 21).)
  • Retention rates(Duration of recruitment and intervention phases (9 weeks).)
  • Body composition(Baseline (week 0) and post-intervention (week 9).)
  • Waist circumference(Baseline (week 0) and post-intervention (week 9).)
  • Motivational regulations: Behavioral Regulation in Exercise Questionnaire (BREQ-2R; Markland & Tobin, 2004; Wilson, Rodgers, Loitz, & Scime, 2006)(Baseline (week 0), post-intervention (week 9), and follow-up (week 21).)
  • Recruitment rates(Duration of recruitment and intervention phases (9 weeks).)
  • Acceptability: Open ended questions(Duration of recruitment and intervention phases (9 weeks).)
  • Body mass(Baseline (week 0) and post-intervention (week 9).)

研究者

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

Jennifer Brunet

Associate Professor

University of Ottawa

研究点 (1)

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