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临床试验/NCT03248752
NCT03248752已完成不适用

Physical Activity Promotion Through Wearable Monitors: A Test of Self and Partner Monitoring Strategies.

University of Victoria2 个研究点 分布在 1 个国家目标入组 34 人开始时间: 2017年7月4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
34
试验地点
2
主要终点
Change from baseline in participants' weekly physical activity participation at 3 months.

研究概览

简要总结

The purpose of this study is to examine the effect of monitoring and sharing physical activity outcomes (using Fitbit technology) with a domestic partner on physical activity participation.

Primary research question: Does sharing physical activity outcomes from wearable technology with a participant's partner improve overall physical activity over 3 months compared to not sharing outcomes? Physical activity will be measured as minutes of moderate to vigorous physical activity per week.

Hypothesis: Knowledge that physical activity outcomes are visible to a participant's partner will serve as a proxy-supervision intervention. Awareness of partner's progress will serve as further motivation. Both factors will improve physical activity adherence in comparison to participants without shared outcomes.

详细描述

Background: Physical activity is associated with management and/or prevention of over 25 chronic health conditions; however the majority of adults in North America are not active enough to experience these benefits. Behavioral strategies have been shown to be effective for increasing physical activity, and wearable fitness monitors such as Fitbits include components of several behavioral strategies including goal setting and feedback. While this technology provides a platform for implementing self-regulation techniques important for behavior change, direct supervision is still the most effective strategy for behavior change. Supervised exercise programs and personal trainers may not be accessible or affordable for people; this study will examine whether proxy supervision by a partner is effective in changing behavior compared to self-regulation alone.

Target Population: Sedentary adults aged 45-75 years old living in Victoria, British-Columbia, Canada.

Sample Size: 80 participant pairs (160 total participants), 40 pairs per group (80 participants per group).

Intervention: Participants will be randomized to two groups: 1 - Self Monitored, 2 - Partner monitored. Both groups will receive an intervention with Group 1 (Self monitored) serving as the comparison group. Participants from both groups will wear an accelerometer for 1 week and complete an online questionnaire at baseline, 6 weeks, and 3 months. Measures of height, weight, waist circumference, and resting blood pressure and heart rate will be taken at baseline and 3 months. Participants will all receive a Fitbit activity tracker and wear it for 3 months. Group 2 (Partner monitor) participants will also have access to their partner's daily progress, receive eachother's Weekly Fitbit reports, and engage in a weekly discussion related to their Weekly Fitbit Report.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
45 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • One or both partners currently not meeting the Canadian Physical Activity Guidelines of 150 minutes of moderate to vigorous physical activity per week
  • Currently living in Victoria, BC
  • Safe to participate in physical activity (physician clearance required if applicable)

排除标准

  • No smartphone or tablet device (with bluetooth technology)
  • No email address
  • No partner and/or not living with partner

结局指标

主要结局

Change from baseline in participants' weekly physical activity participation at 3 months.

时间窗: Baseline, 6 weeks, and 3 months

Quantified as minutes of moderate to vigorous physical activity measured with accelerometry. Participants will wear an accelerometer for a minimum of 10 hours per day for 7 consecutive days. Changes in this measure will be examined (3 months to baseline, 3 months to 6 weeks, 6 weeks to baseline).

次要结局

  • Change in Body Mass Index from baseline to 3 months.(Baseline and 3 months)
  • Change in quality of life from baseline to 3 months measured using the Short Form 12 questionnaire.(Baseline, 6 weeks, 3 months)
  • Change in physical activity beliefs, attitudes, barriers, and motivation from baseline to 3 months.(Baseline, 6 weeks, 3 months)
  • Change in physical activity habits from baseline to 3 months.(Baseline, 6 weeks, 3 months)
  • Change in waist circumference from baseline to 3 months.(Baseline, 3 months)
  • Change in self-reported physical activity from baseline to 3 months.(Baseline, 6 weeks, 3 months.)
  • Change in mood from baseline to 3 months measured using the Hospital Anxiety and Depression Scale in a questionnaire.(Baseline, 6 weeks, 3 months)
  • Change in life satisfaction from baseline to 3 months measured using Diener's satisfaction with life scale in a questionnaire.(Baseline, 6 weeks, 3 months)
  • Change in physical activity behaviour regulation from baseline to 3 months.(Baseline, 6 weeks, 3 months)
  • Change in physical activity identity from baseline to 3 months.(Baseline, 6 weeks, 3 months)

研究者

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

Ryan Rhodes

Professor, Principal Investigator

University of Victoria

研究点 (2)

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