NCT04277091

Brief Summary

Cycling and running-based high-intensity interval training are well-established to improve a variety of health outcomes. However, the efficacy of upper-body high-intensity interval training, vital for individuals with lower-body impairments, has yet to be well-characterized. The purpose of this study is to compare the effect of a single bout of upper-body high-intensity interval exercise (HIIE) in comparison to traditional moderate-intensity continuous exercise (MICE) on the blood response (e.g. glucose, insulin, fats) following a meal. This study is recruiting able-bodied adults (aged 18-65 years). Participants will need to attend the laboratory at the University of Bath for two preliminary sessions, and three main study trials.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
11

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Oct 2019

Geographic Reach
1 country

1 active site

Status
completed

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

Study Start

First participant enrolled

October 21, 2019

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

February 10, 2020

Completed
10 days until next milestone

First Posted

Study publicly available on registry

February 20, 2020

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2021

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2021

Completed
Last Updated

July 27, 2022

Status Verified

July 1, 2022

Enrollment Period

1.2 years

First QC Date

February 10, 2020

Last Update Submit

July 26, 2022

Conditions

Keywords

postprandial metabolism

Outcome Measures

Primary Outcomes (1)

  • Postprandial triglyceride concentrations

    Postprandial triglyceride concentrations in serum samples

    5 hours

Secondary Outcomes (8)

  • Postprandial glucose concentrations

    5 hours

  • Postprandial insulin concentrations

    5 hours

  • Postprandial substrate oxidation

    5 hours

  • Rating of Perceived Exertion

    HIIE: End of Warm-Up, 8 min, 12 min, 16 min, 20 min, 24 min. MICE: 0, 20, 40, 60, 80, 100% through exercise session (exact time points dependent on exercise time for each participant)

  • Heart Rate

    HIIE: End of Warm-Up, 8 min, 12 min, 16 min, 20 min, 24 min. MICE: 0, 20, 40, 60, 80, 100% through exercise session (exact time points dependent on exercise time for each participant)

  • +3 more secondary outcomes

Study Arms (3)

Control

NO INTERVENTION

No exercise

High-intensity interval exercise

EXPERIMENTAL

10 x 60 s intervals at 80% peak power output (interspersed with 60 s recovery intervals at 10% peak power output)

Other: High-intensity interval training

Moderate-intensity continous exercise

EXPERIMENTAL

50% peak power output (duration determined to elicit same energy expenditure as high-intensity interval exercise condition)

Other: Moderate-intensity continuos training

Interventions

Arm-cranking exercise

High-intensity interval exercise

Arm-cranking exercise

Moderate-intensity continous exercise

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Non-smoker
  • No history of cardiovascular, metabolic, or neuromuscular disease

You may not qualify if:

  • Individuals with a nut allergy

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department for Health

Bath, BA2 7AY, United Kingdom

Location

MeSH Terms

Interventions

High-Intensity Interval Training

Intervention Hierarchy (Ancestors)

Physical Conditioning, HumanExerciseMotor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Officials

  • James Bilzon

    University of Bath

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

February 10, 2020

First Posted

February 20, 2020

Study Start

October 21, 2019

Primary Completion

January 1, 2021

Study Completion

January 1, 2021

Last Updated

July 27, 2022

Record last verified: 2022-07

Locations