跳至主要内容
临床试验/NCT04865666
NCT04865666已完成不适用

Examining the Real-World Effectiveness of the Movr mHealth Application: A Mixed-Methods Pilot Pragmatic Randomized Controlled Trial

University of British Columbia1 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2019年9月25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
48
试验地点
1
主要终点
Change from baseline in functional movement screen (FMS) at 8-week follow-up

研究概览

简要总结

The objective of this 8-week pilot pragmatic randomized controlled trial was to examine the real-world impact of movr on functional movement, flexibility, strength, and cardiovascular fitness.

详细描述

Thousands of mobile apps available for download are geared towards health and fitness, yet limited research has evaluated the real-world effectiveness of such apps. The movr app is an mHealth app designed to enhance physical functioning by prescribing functional movement training based on individualized movement assessments. movr's influence on functional movement and physical fitness (flexibility, strength, and cardiovascular fitness) has not yet been established empirically. Thus, the objective of this 8-week pilot pragmatic randomized controlled trial was to examine the real-world impact of movr on functional movement, flexibility, strength, and cardiovascular fitness.

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
None

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Ages 18 to 50 years
  • •Ability to read and write English
  • •Owned a mobile device that could download applications from the App Store or Google Play

排除标准

  • •Previously used the movr app
  • •Had any contraindications to exercise based on the Get Active Questionnaire

研究组 & 干预措施

movr App Group

Experimental

Participants were instructed to maintain their usual physical activity, diet, and sleep behavior for the 8-week intervention period and to avoid any specialized exercise training for that time period, but they were also asked to use the movr app to supplement their current activity.

干预措施: movr mHealth App (Device)

Waitlist Control Group

No Intervention

Participants were instructed to maintain their usual physical activity, diet, and sleep behavior over the 8-week study period and to avoid any specialized exercise training for that time period. Following the 8-week study period, individuals in the control group were permitted to download and use the movr app if they chose to.

结局指标

主要结局

Change from baseline in functional movement screen (FMS) at 8-week follow-up

时间窗: Baseline and 8-week follow-up

The 100-point version of the functional movement screen (FMS) was used to identify individual movement patterns. The FMS is a screening tool to assess full body movement patterns and consists of seven core movement tests (deep squat, hurdle step, in-line lunge, active straight-leg raise, shoulder flexibility, trunk stability push-up, and quadruped rotary stability). The seven FMS movement screens were performed by each participant and recorded using a portable observation lab (Noldus) with two video cameras (one shot on a sagittal plane \[side\] view and the other from a frontal plane \[front/back\] view). The standardized FMS verbal instructions were provided by the researcher. The video-based testing was completed to minimize participant burden during lab visits and to blind participants to their FMS scores for each of the movements. Scoring of the FMS was completed at a later time using the video recordings.

次要结局

  • Changes from baseline in health locus of control at 8-week follow-up(Baseline and 8-week follow-up)
  • Changes from baseline in perceptions of health at 8-week follow-up(Baseline and 8-week follow-up)
  • Change from baseline in muscular endurance at 8-week follow-up(Baseline and 8-week follow-up)
  • Change from baseline in flexibility at 8-week follow-up(Baseline and 8-week follow-up)
  • Change from baseline in handgrip strength at 8-week follow-up(Baseline and 8-week follow-up)
  • Semi-structured interviews completed at baseline and 8-week follow-up(Baseline and 8-week follow-up)
  • Change from baseline in cardiovascular fitness at 8-week follow-up(Baseline and 8-week follow-up)
  • Changes from baseline in physical activity enjoyment at 8-week follow-up(Baseline and 8-week follow-up)
  • Change from baseline in lower body power at 8-week follow-up(Baseline and 8-week follow-up)
  • Changes from baseline in well-being, enjoyment, satisfaction with physical functioning at 1, 2, 3, 4, 5, 6, 7, and 8-week follow-up(Baseline and 1, 2, 3, 4, 5, 6, 7, and 8-week follow-up)

研究者

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

Mary Jung

Associate Professor

University of British Columbia

研究点 (1)

Loading locations...

相似试验