Tokyo, Dec. 31 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000060156) titled 'Elucidation of Molecular Mechanisms Underlying Exercise-Induced Mood Improvement Using a Human Knockout Model' on Dec. 31.
Study Type:
Interventional
Study Design:
Basic Design - Cross-over
Randomization - Randomized
Blinding - Open -no one is blinded
Control - No treatment
Primary Sponsor:
Institute - Yamanashi Gakuin University
Condition:
Condition - Healthy adult men
Classification by malignancy - Others
Genomic information - YES
Objective:
Narrative objectives1 - This study biochemically investigates whether endocannabinoids (eCBs) mediate acute exercise-induced mood improvement, utilizing a human knockout model based on gene expression capacity.
Basic objectives2 - Efficacy
Intervention:
Interventions/Control_1 - Participants will perform cycle ergometer exercise at 40% heart rate reserve for 30 minutes in the exercise condition, and maintain a resting state for 30 minutes in the control condition.
Interventions/Control_2 - Magnetic resonance spectroscopy (MRS) will be performed after the intervention. During the MRS acquisition, mood fluctuations will be induced using the Open Affective Standardized Image Set (OASIS).
Eligibility:
Age-lower limit - 18
years-old
=
Gender - Male
Key inclusion criteria - Untrained individuals
Key exclusion criteria - Individuals with abnormal findings in medical check-ups.
Individuals currently taking medication.
Current smokers.
Individuals unable to perform exercise at the prescribed intensity.
Individuals with a history of vasovagal reflex (fainting) during blood sampling.
Target Size - 60
Recruitment Status:
Recruitment status - Preinitiation
Date of protocol fixation - 2025 Year 12 Month 21 Day
Date of IRB - 2025 Year 12 Month 01 Day
Anticipated trial start date - 2026 Year 03 Month 01 Day
Last follow-up date - 2028 Year 03 Month 31 Day
To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000068801
Disclaimer: Curated by HT Syndication.