- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06069427
The Effect of Reducing Total Volume of Sprint Exercise on Circulating Levels of BDNF
May 7, 2024 updated by: Niels Vollaard, University of Stirling
The Effect of Reducing Total Volume of Sprint Exercise in Sprint Interval Training Protocols on Circulating Levels of Brain-derived Neurotrophic Factor (BDNF)
Regular exercise is well known to be required for good physical health, but exercise can also improve mental health.
Although the effects of exercise on mental health have been shown in many studies, it remains unclear how exercise improves mental health.
In recent years, the potential role of a specific protein called 'brain-derived neurotrophic factor' (BDNF) has received increasing attention.
Higher levels of BDNF in the blood are associated with better cognitive performance, attention, and spatial memory.
Conversely, low levels of BDNF in the blood are found in patients with depression, dementia, mild cognitive impairment, and Alzheimer's disease.
BDNF can be released during exercise, with greater increases after exercise performed at higher intensities.
For example, classic sprint interval training (SIT), which involves four 30-second 'all-out' cycle sprints, has been shown to lead to greater increases in BDNF compared to moderate or vigorous exercise.
Although these results suggest that SIT is an effective way to increase BDNF, SIT is not generally considered feasible for patients or untrained members of the general public, because it is a very tiring type of exercise.
However, other more manageable protocols have been developed, such as the 'reduced-exertion, high-intensity interval training' (REHIT) protocol, which involves two 20-second 'all-out' sprints within a 10-minute low-intensity exercise session.
Although it is clear that BDNF levels increase in an intensity-dependent manner in response to exercise, the effect of exercise volume remains unknown.
Exercise intensity is identical for SIT and REHIT, but if BDNF levels increase to a similar extent in response to both protocols, REHIT would constitute a more feasible intervention for use in patients and the general public.
The aim of the present study is to compare the effects of REHIT vs. classic SIT on levels of BDNF in the blood.
For this,15 study participants will be recruited, who will each complete a SIT session, a REHIT session, and a no-exercise control session.
Levels of BDNF will be measured in blood samples taken at rest, as well as directly after exercise, 30 minutes after exercise, and 90 minutes after exercise.
It will be determined whether the greater amount of sprint exercise in a SIT session will be associated with a greater increase in levels of BDNF in the blood compared to the REHIT session which consists of a lower amount of sprint exercise.
Study Overview
Status
Active, not recruiting
Conditions
Study Type
Interventional
Enrollment (Actual)
13
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Midlothian
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Stirling, Midlothian, United Kingdom, FK9 4LA
- University of Stirling
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Apparently health young male volunteers
Exclusion Criteria:
- Age <18 y or >40 y
- BMI > 35 kg/m2
- participation in a structured exercise training programme at any time in the preceding 6 months
- suffering from acute (e.g., common cold, Covid-19, flu, etc) or chronic disease (e.g., diabetes, heart disease, cancer, etc)
- answering 'yes' to one or more questions of a standard physical activity readiness questionnaire (PAR-Q)
- resting heart rate ≥100 bpm
- clinically significant hypertension (>140/90 mm Hg)
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Area under the plasma concentration versus time curve (AUC) of BDNF
Time Frame: Pre-exercise, directly post-exercise, and 30 and 90 minutes post-exercise
|
Plasma levels of the protein brain-derived neurotrophic factor (BDNF) will be measured pre-exercise, directly post-exercise, and 30 and 90 minutes post-exercise.
The area-under-the-curve for plasma BDNF will be calculated.
Differences in AUC between the 3 trails will be determined.
|
Pre-exercise, directly post-exercise, and 30 and 90 minutes post-exercise
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Niels Vollaard, PhD, University of Stirling
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 15, 2023
Primary Completion (Estimated)
July 30, 2024
Study Completion (Estimated)
December 31, 2024
Study Registration Dates
First Submitted
September 27, 2023
First Submitted That Met QC Criteria
October 4, 2023
First Posted (Actual)
October 5, 2023
Study Record Updates
Last Update Posted (Actual)
May 8, 2024
Last Update Submitted That Met QC Criteria
May 7, 2024
Last Verified
May 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- 14395
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
There is no plan to share individual participant data.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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