search
Back to results

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

Primary Purpose

Resistance Training

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Bodyweight exercises (push-ups, angled-rows, bodyweight squats) on weekdays
Sponsored by
Edward Via Virginia College of Osteopathic Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Resistance Training

Eligibility Criteria

19 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • 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.

Exclusion Criteria:

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

Sites / Locations

  • Auburn University
  • Edward Via College of Osteopathic Medicine-Auburn Campus

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention Arm

Waitlist Control Arm

Arm Description

Participants in this arm will be instructed to perform one set each of push-ups, angled-rows and bodyweight squats every weekday without supervision for a total of 24 weeks. They will receive the equipment necessary to perform the exercises as well as guidance on proper performance. They will also receive training in the Tiny Habits® Method at baseline and digital coaching for the duration of the study.

Participants in the control arm will be instructed to refrain from resistance training for the initial 12 weeks of the study. Note that, after the 12-week follow-up assessment (at which the primary outcome of composite reps will be assessed), this group will begin the RT program. They will receive the same equipment, training, and coaching as the intervention group, and they will continue the RT program for 12 weeks, followed by a 24-week assessment.

Outcomes

Primary Outcome Measures

Physical strength
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.

Secondary Outcome Measures

Physical strength
The change in physical strength baseline to 24-week follow-up, in the intervention group, and from 12-week follow-up to 24-week follow-up, in the waitlist control group, 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 at those timepoints.
Blood pressure
Measure at baseline, 12-week, and 24-week follow-up following guideline recommendations and using a calibrated automated blood pressure cuff.
Lipid profile
Total cholesterol, (calculated) LDL, HDL, and triglycerides measured at baseline, 12-week, and 24-week follow-up using the CardioChek Plus Analyzer.
Hemoglobin A1c
Measured at baseline, 12-week, and 24-week follow-up using the PTS Diagnostics A1CNow+ System.
Habit strength
Each week during the initial 12-weeks of their intervention phase, participants will complete a survey that, among other things, assesses change in habit strength regarding exercise performance (push-ups, angled-rows, bodyweight squats), via the validated Self-Report Behavioral Automaticity Index (SRBAI).
Adherence to protocol
Each week during the initial 12-weeks of their intervention phase, participants will complete a survey that, among other things, will assess their (self-reported) adherence to the resistance-training protocol.
Satisfaction with program
Each week during the initial 12-weeks of their intervention phase, participants will complete a survey that, among other things, is meant to assess their level of satisfaction with the program.

Full Information

First Posted
December 16, 2019
Last Updated
April 16, 2021
Sponsor
Edward Via Virginia College of Osteopathic Medicine
Collaborators
Auburn University
search

1. Study Identification

Unique Protocol Identification Number
NCT04207567
Brief Title
Minute Calisthenics: A Daily, Habit-Based, Bodyweight Resistance-Training Program
Official Title
Minute Calisthenics: A Daily, Habit-Based, Bodyweight Resistance-Training Program
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Completed
Study Start Date
November 11, 2019 (Actual)
Primary Completion Date
September 20, 2020 (Actual)
Study Completion Date
January 4, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Edward Via Virginia College of Osteopathic Medicine
Collaborators
Auburn University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed Description
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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Resistance Training

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants will be randomized (1:1) to an intervention or waitlist control group. The intervention group will perform one set of the bodyweight exercises (i.e., push-ups, angled-rows, bodyweight squats), with training and coaching, unsupervised every weekday for 12 weeks. The waitlist control group will refrain from resistance training for the initial 12. After a 12-week follow-up assessment, the intervention group will continue the RT program for an additional 12 weeks, and the waitlist control group will initiate the RT program and continue for 12 weeks. A 24-week follow-up assessment will then be conducted.
Masking
Outcomes Assessor
Masking Description
The researchers assessing outcomes as well as the researcher performing statistical analysis will be blinded to participants' group assignment.
Allocation
Randomized
Enrollment
47 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention Arm
Arm Type
Experimental
Arm Description
Participants in this arm will be instructed to perform one set each of push-ups, angled-rows and bodyweight squats every weekday without supervision for a total of 24 weeks. They will receive the equipment necessary to perform the exercises as well as guidance on proper performance. They will also receive training in the Tiny Habits® Method at baseline and digital coaching for the duration of the study.
Arm Title
Waitlist Control Arm
Arm Type
No Intervention
Arm Description
Participants in the control arm will be instructed to refrain from resistance training for the initial 12 weeks of the study. Note that, after the 12-week follow-up assessment (at which the primary outcome of composite reps will be assessed), this group will begin the RT program. They will receive the same equipment, training, and coaching as the intervention group, and they will continue the RT program for 12 weeks, followed by a 24-week assessment.
Intervention Type
Behavioral
Intervention Name(s)
Bodyweight exercises (push-ups, angled-rows, bodyweight squats) on weekdays
Intervention Description
Participants will be instructed to perform one set each of push-ups, angled-rows, and bodyweight squats every weekday. They will be given the equipment and training necessary to properly perform the exercises. They will also be trained in the Tiny Habits® Method and receive digital coaching.
Primary Outcome Measure Information:
Title
Physical strength
Description
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.
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Physical strength
Description
The change in physical strength baseline to 24-week follow-up, in the intervention group, and from 12-week follow-up to 24-week follow-up, in the waitlist control group, 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 at those timepoints.
Time Frame
Up to 24 weeks
Title
Blood pressure
Description
Measure at baseline, 12-week, and 24-week follow-up following guideline recommendations and using a calibrated automated blood pressure cuff.
Time Frame
Baseline, 12-week, and 24-week follow-up
Title
Lipid profile
Description
Total cholesterol, (calculated) LDL, HDL, and triglycerides measured at baseline, 12-week, and 24-week follow-up using the CardioChek Plus Analyzer.
Time Frame
Baseline, 12-week, and 24-week follow-up
Title
Hemoglobin A1c
Description
Measured at baseline, 12-week, and 24-week follow-up using the PTS Diagnostics A1CNow+ System.
Time Frame
Baseline, 12-week, and 24-week follow-up
Title
Habit strength
Description
Each week during the initial 12-weeks of their intervention phase, participants will complete a survey that, among other things, assesses change in habit strength regarding exercise performance (push-ups, angled-rows, bodyweight squats), via the validated Self-Report Behavioral Automaticity Index (SRBAI).
Time Frame
12 weeks
Title
Adherence to protocol
Description
Each week during the initial 12-weeks of their intervention phase, participants will complete a survey that, among other things, will assess their (self-reported) adherence to the resistance-training protocol.
Time Frame
12 weeks
Title
Satisfaction with program
Description
Each week during the initial 12-weeks of their intervention phase, participants will complete a survey that, among other things, is meant to assess their level of satisfaction with the program.
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 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. Exclusion Criteria: Pregnant Participation in structured resistance training for ≥2 days/week, on average, during the past year. Implanted medical device (e.g., pacemaker, defibrillator).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Joshua C Hollingsworth, PharmD, PhD
Organizational Affiliation
Edward Via College of Osteopathic Medicine (VCOM-Auburn)
Official's Role
Principal Investigator
Facility Information:
Facility Name
Auburn University
City
Auburn
State/Province
Alabama
ZIP/Postal Code
36832
Country
United States
Facility Name
Edward Via College of Osteopathic Medicine-Auburn Campus
City
Auburn
State/Province
Alabama
ZIP/Postal Code
36832
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
30418471
Citation
Piercy KL, Troiano RP, Ballard RM, Carlson SA, Fulton JE, Galuska DA, George SM, Olson RD. The Physical Activity Guidelines for Americans. JAMA. 2018 Nov 20;320(19):2020-2028. doi: 10.1001/jama.2018.14854.
Results Reference
background
PubMed Identifier
30702833
Citation
National Center for Health Statistics (US). Health, United States, 2017: With Special Feature on Mortality [Internet]. Hyattsville (MD): National Center for Health Statistics (US); 2018. Available from http://www.ncbi.nlm.nih.gov/books/NBK532685/
Results Reference
background
PubMed Identifier
22777332
Citation
Westcott WL. Resistance training is medicine: effects of strength training on health. Curr Sports Med Rep. 2012 Jul-Aug;11(4):209-16. doi: 10.1249/JSR.0b013e31825dabb8.
Results Reference
background
PubMed Identifier
32799849
Citation
Hollingsworth JC, Young KC, Abdullah SF, Wadsworth DD, Abukhader A, Elfenbein B, Holley Z. Protocol for Minute Calisthenics: a randomized controlled study of a daily, habit-based, bodyweight resistance training program. BMC Public Health. 2020 Aug 15;20(1):1242. doi: 10.1186/s12889-020-09355-4.
Results Reference
derived

Learn more about this trial

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

We'll reach out to this number within 24 hrs