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Comparing the Acute Effects of Moderate-Intensity Aerobic Exercise and Energy Drink Consumption on Mood and Cognitive Outcomes in Healthy Young Adults.

Comparing the Acute Effects of Moderate-Intensity Aerobic Exercise and Energy Drink Consumption on Mood and Cognitive Outcomes in Healthy Young Adults

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20260603003
Enrollment
24
Registered
2026-06-03
Start date
2026-05-06
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute cognitive fatigue, impaired concentration, and mood disturbances associated with periods of high academic demand in healthy young adults

Interventions

Participants randomized to this sequence will receive Intervention A in week one and cross over to Intervention B in week two. Intervention A involves consuming one standard two hundred fifty millilit
Experimental Other,Experimental Other
Sequence AB Energy Drink followed by Aerobic Exercise,Sequence BA Aerobic Exercise followed by Energy Drink

Sponsors

Self funded
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 25 Years

Inclusion criteria

Inclusion criteria: 1. Healthy university students aged 18 to 25 years. 2. Able to perform light to moderate aerobic exercise safely. 3. Able to consume a caffeine containing energy drink without known medical issues. 4. Have normal or corrected to normal vision and hearing. 5. Able to understand the study instructions and provide written informed consent. 6. Fluent in English, the language used for testing. 7. Medically stable based on medical history and a MAHSA medical check up.

Exclusion criteria

Exclusion criteria: 1. Have a history of cardiovascular, respiratory, neurological, or psychiatric disorders. 2. Have caffeine intolerance, allergy, or sensitivity. 3. Are a chronic smoker and/or regular alcohol drinker. 4. Are taking medications or supplements affecting cognition, mood, or HR. 5. Have a history of fainting, dizziness, arrhythmia, or exercise intolerance. 6. Have a recent injury or illness preventing exercise participation. 7. Are pregnant or breastfeeding.

Design outcomes

Primary

MeasureTime frame
Mood states 20 and 30 min after interventions Mood states will be determined using two questionnaires. Bond-Lader Visual Analogue Scale (VAS) and Profile of Mood States (POMS)

Secondary

MeasureTime frame
Cognitive function 20 and 30 min after interventions Cognitive Drug Research Computerized Assessment System COGDRAS by Inquisit Lab 7 Millisecond Software Seven computerized cognitive tests assessing attention and memory

Countries

Malaysia

Contacts

Public ContactYe Htut Linn

MAHSA University

hlye@mahsa.edu.my01140618587

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026