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临床试验/NCT04207567
NCT04207567已完成不适用

Minute Calisthenics: A Daily, Habit-Based, Bodyweight Resistance-Training Program

Edward Via Virginia College of Osteopathic Medicine4 个研究点 分布在 1 个国家目标入组 47 人开始时间: 2019年11月11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
47
试验地点
4
主要终点
Physical strength

研究概览

简要总结

As the primary objective, this study will evaluate the effectiveness, in terms of changes in physical strength, of a resistance training (RT) program consisting of brief bodyweight exercises (<5 min/day) performed unsupervised every weekday for 12 weeks. Blood pressure, lipid profile, hemoglobin A1ca, habit strength and satisfaction with the program will also be assessed. Office workers and osteopathic medical students will serve as participants.They will be randomized (1:1) to the intervention group or to a waitlist control group that will refrain from RT for the initial 12 weeks. After the 12-week follow-up assessment, the intervention group will continue the program and the waitlist control group will start the program for 12 weeks, followed by a 24-week follow-up assessment.

详细描述

Regular resistance training (RT) provides significant health benefits. However, roughly 3 out of 4 US adults do not meet current US Physical Activity Guidelines regarding RT. Studies are needed that assess the effectiveness and feasibility of RT programs that are time-efficient and simple to perform.

This will be a randomized controlled study of a habit-based RT program consisting of one set each of push-ups, angled-rows, and bodyweight squats performed every weekday for 12 weeks. Forty to 60 office workers and osteopathic medical students, who currently do not engage in RT, will be recruited, assessed, and randomized (1:1) to an intervention group, which will perform the exercises as just described, or a waitlist control group, which will refrain from RT for 12 weeks. To promote consistent exercise performance, the intervention group will be trained in the Tiny Habits® Method (a systematic approach to adding new behaviors in one's daily routine) and receive digital coaching for the duration of the study.

After the 12-week follow-up assessment, the intervention group will continue the program for an additional 12 weeks, and the waitlist control group will start the program and continue for 12 weeks, including Tiny Habits training and digital coaching. A 24-week follow-up assessment will then be conducted.

The primary outcome of interest is the change from baseline to 12-weeks in physical strength from, as measured by the maximum number of composite repetitions (i.e., push-ups + angled-rows + bodyweight squats) performed under a standardized protocol. Secondary outcomes of interest include adherence to and satisfaction with the program, and change from baseline to 12- and 24-week follow-up in composite repetitions, habit strength, blood pressure, lipid panel, hemoglobin A1c, body mass index, anthropometry, body composition, and mid-thigh muscle thickness

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)

盲法说明

The researchers assessing outcomes as well as the researcher performing statistical analysis will be blinded to participants' group assignment.

入排标准

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

入选标准

  • Office worker or osteopathic medical student at the local college/university
  • Demonstrate ability to properly perform 1 repetition of each exercise (push-ups, angled-rows, bodyweight squats).
  • Indicate having motivation and confidence in ability to perform exercises on weekdays.
  • Low adverse event risk while participating, as assessed via the Physical Activity Readiness-Questionnaire (PAR-Q)
  • Must be able to identify a suitable location (either at home, school, or office) to set up the suspension system needed to perform the angled-row exercise.

排除标准

  • Participation in structured resistance training for ≥2 days/week, on average, during the past year.
  • Implanted medical device (e.g., pacemaker, defibrillator).

结局指标

主要结局

Physical strength

时间窗: 12 weeks

As the primary outcome, the change in physical strength in the intervention group vs. the control group from baseline to 12-week follow-up will be determined by assessing the maximum number of composite repetitions (i.e., push-ups + angled rows + bodyweight squats) that the participant is able to perform under a standardized protocol.

次要结局

  • Hemoglobin A1c(Baseline, 12-week, and 24-week follow-up)
  • Satisfaction with program(12 weeks)
  • Physical strength(Up to 24 weeks)
  • Lipid profile(Baseline, 12-week, and 24-week follow-up)
  • Adherence to protocol(12 weeks)
  • Blood pressure(Baseline, 12-week, and 24-week follow-up)
  • Habit strength(12 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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