Use of Exercise Snacks to Improve Upper Body Fitness
Use of Resistive Exercise Snacks to Improve Upper Body Fitness in Graduate Students
1 other identifier
interventional
50
1 country
1
Brief Summary
This study will examine the effects of an upper-body resistance "exercise snack" (ES) protocol on upper-body strength, endurance, and power. Participants will be randomly assigned to one of three groups: a submaximal effort repeated throughout the exercise day ES group, a maximal effort performed once per exercise day ES group, and a control group that continues usual activity (Control: no resistance exercise). Both exercise groups will perform two exercises, push-ups and planks, three days per week. The submaximal repeated effort ES group (SMR\_ES) will perform approximately 33% of the maximal number of push-ups and maintain a plank position for 33% of maximal time, three times per day. The maximal once-per-day effort ES group (MO\_ES) will perform the maximal number of push-ups and maintain a plank position for maximal time, once per day. Therefore, both ES groups (SMR\_ES and MO\_ES) will perform the same weekly volume (repetitions and time) of both exercises across the six-week intervention period. Before and after the six-week intervention period, all participants will undergo testing to assess upper-body performance. Outcome measures will include push-up endurance (maximum repetitions), plank endurance (maximum time), push-up power (assessed using force plates), and maximal push strength (assessed using hand-held dynamometry). Pre- and post-intervention changes in outcomes will be compared among all three groups. If significant changes are identified, additional comparisons will be conducted between the SMR\_ES and Control groups, as well as between the SMR\_ES and MO\_ES groups. The primary aim of this study is to determine whether repeated submaximal efforts performed three times per day, three days per week, increase upper-body endurance, power, and strength compared to a control group performing no resistance exercise. The secondary aim is to determine whether submaximal efforts performed three times per day, three days per week, produce changes in upper-body strength, endurance, and power that are not different from maximal efforts performed once per day, three days per week. These aims address whether exercise distribution influences strength and power adaptations beyond total weekly volume. The findings may help inform time-efficient, lower subjective-effort resistance training strategies that can be implemented in educational, athletic, or general fitness settings.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Feb 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 6, 2026
CompletedFirst Posted
Study publicly available on registry
January 23, 2026
CompletedStudy Start
First participant enrolled
February 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 24, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
April 25, 2026
CompletedApril 9, 2026
April 1, 2026
2 months
January 6, 2026
April 6, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Maximal Upper Body Push Strength
Upper-body muscular strength will be assessed using a hand-held dynamometer during a standardized pushing task. Participants will push a barbell upward against an immovable strap connected to a pull dynamometer. Peak force output (Newtons) will be recorded.
Change from baseline after 6 weeks
Push-Up Endurance (Repetitions)
Upper-body muscular endurance will be assessed by the maximum number of push-ups completed using standardized form criteria.
Change from baseline after 6 weeks.
Plank Endurance (Seconds)
Core and upper-body endurance will be assessed by the maximum duration (seconds) participants can maintain a standardized plank position.
Change from baseline after 6 weeks
Secondary Outcomes (2)
Upper-Body Power - Peak Force (Newtons)
Change from baseline after 6 weeks.
Upper-Body Power - Time to Task Completion (Seconds)
Change from baseline after 6 weeks
Other Outcomes (3)
Upper-Body Power - Mean Force (Newtons)
Observed over 6 weeks.
Participant Retention (%)
Observed over 6 weeks
Protocol Adherence (%)
Observed over 6 weeks
Study Arms (3)
A submaximal repeated effort exercise snack (SMR_ES)
EXPERIMENTALThe SMR\_ES group will perform approximately 33% of their individual number of maximal push-up and maximal plank time, three times per day, three days per week.
A maximal effort one-time exercise snack (MO_ES)
EXPERIMENTALThe MO\_ES group will perform the maximal number of push-ups and hold a plank position for their maximal time, once per day, three days per week.
Control group
NO INTERVENTIONContinues usual activity with no upper body resistive exercise.
Interventions
Participants perform frequent, low-dose submaximal upper-body exercise snacks spread throughout the day. The SMR\_ES group will perform approximately 33% of their individual number of maximal push-up and maximal plank time, three times per day, three days per week.
Participants perform a single daily maximal-effort upper-body exercise snack. The MO\_ES group will perform the maximal number of push-ups and hold a plank position for their maximal time, once per day, three days per week.
Eligibility Criteria
You may qualify if:
- Healthy, as determined by self-reported health history
- Enrolled as a college or university student (full-time or part-time)
- Not currently participating in a structured upper-body resistance training program
- No participation in upper-body resistance training (e.g., weightlifting, calisthenics, CrossFit, bodyweight strength programs) for ≥ 3 months prior to study enrollment
- Willing and able to perform maximal and submaximal push-up and plank exercises
- Willing to refrain from initiating any new upper-body resistance training during the study period
- Able to provide written informed consent
You may not qualify if:
- Current participation in an upper-body resistance training program or engagement in upper-body strength training within the past 3 months
- History of upper extremity, shoulder, elbow, wrist, or trunk injury within the past 6 months that could limit exercise performance
- History of neurological, cardiovascular, metabolic, or musculoskeletal disorders that contraindicate resistance exercise
- Current pain or discomfort in the shoulders, elbows, wrists, hands, neck, or low back during pushing or plank activities
- Previous surgery to the upper extremities or spine within the past 12 months
- Use of medications that may significantly affect muscle performance, fatigue, or neuromuscular function
- Pregnancy or suspected pregnancy
- Any condition deemed by the investigators to pose an increased risk during maximal or repeated resistance exercise
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
New York Institute of Technology
Old Westbury, New York, 11568, United States
Related Publications (42)
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Study Officials
- PRINCIPAL INVESTIGATOR
Alexander Rothstein
New York Institute of Technology
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
January 6, 2026
First Posted
January 23, 2026
Study Start
February 1, 2026
Primary Completion
March 24, 2026
Study Completion
April 25, 2026
Last Updated
April 9, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP
- Time Frame
- The information will be available May 2026 and remain for 5 years.
- Access Criteria
- Access will require access to DryAd or a request for access to the researchers.
We will upload our shared anonymized data using DryAd.