Acute Effects of PLT Health Solutions zümXR Extended-Release Caffeine
Launched by APPLIED SCIENCE & PERFORMANCE INSTITUTE · May 29, 2024
Trial Information
Current as of July 22, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying the effects of two different types of caffeine: an extended-release version (ER-CAFF) and an immediate-release version (IR-CAFF). Researchers want to see how these types of caffeine impact mood, alertness, and cognitive (thinking and memory) abilities, especially after a night of poor sleep. The study will involve healthy men and women between the ages of 35 and 50 who usually consume moderate amounts of caffeine. Participants will be asked to have less than five hours of sleep before coming to the lab for two visits, where they will take either type of caffeine and undergo various tests to measure its effects.
To be eligible for the study, individuals should have a body mass index (BMI) between 18.5 and 29.9 and not have a history of anxiety or sleep disorders. Participants will be carefully screened to ensure they meet these criteria. Throughout the study, they'll need to wear a device that tracks their sleep and physical activity. This study is expected to last about two weeks, and there will be a one-week break between the two caffeine types to ensure accurate results. It’s a great opportunity for those who fit the criteria to contribute to research that may help understand how different types of caffeine affect our bodies and minds.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Male or female aged 35-50 years (both limits inclusive);
- • Body mass index (BMI) of 18.50-29.99 kg/m2 -Habitual moderate caffeine consumers (200-400 mg/day) assessed through caffeine assessment tool (Caffeine -
- • Consumption Questionnaire, CCQ);
- • Intermediate chronotype (\>31 or \<69 on Morningness-Eveningness Questionnaire).
- Exclusion Criteria:
- * Subjects presenting any of the following will not be included in the study:
- • No history of anxiety disorders or sleep disorders;
- • Non-smokers;
- • Alcohol consumption 72 hours prior to the start of study/consumption of study product;
- • No use of sleep medicines, melatonin, marijuana within two weeks of start of study;
- • No travel involving time zone change, shift work, or other life events that alter sleep schedule \>3 hours from the norm one week before the start of study (assessed using sleep-wake schedule diary for week prior to study);
- • Caffeine restricted past 12 PM from the day prior to the start of study (verify through caffeine diet history).
About Applied Science & Performance Institute
The Applied Science & Performance Institute (ASPI) is a leading clinical trial sponsor dedicated to advancing the fields of health, nutrition, and performance through rigorous scientific research. With a commitment to innovative methodologies and evidence-based practices, ASPI collaborates with a diverse network of researchers, healthcare professionals, and industry partners to conduct clinical trials that explore cutting-edge interventions and enhance human performance. By prioritizing ethical standards and regulatory compliance, ASPI aims to contribute valuable insights that inform clinical practices and promote optimal health outcomes across various populations.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Tampa, Florida, United States
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported