Sleep Disorders Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You are willing and able to sign a consent form written in English
- You are between 40 and 60 years old
- You are female
- You drink caffeine every day
- You are generally healthy and do not have any significant physical or mental health conditions
Who may not be able to join:
- You currently smoke cigarettes or use a vaping device
- You have a known allergy or intolerance to any of the food or drink products used in the trial
- You are not willing to drink coffee as part of the trial
- You have been diagnosed with a psychiatric or mental health condition
- You use recreational drugs
- You have been diagnosed with a heart or circulatory condition, such as heart disease or high blood pressure
- You are currently taking any prescribed medication, except for contraceptives or hormone replacement therapy (HRT)
- You have Raynaud's disease or any other condition affecting your circulation
- You have had an injury or infection in your hand or arm within the last month
- You have a chronic pain condition, or you experience severe numbness or pain when exposed to cold temperatures
- You have previously had a brain injury or brain surgery
- You work night shifts
- You are currently pregnant or breastfeeding
- You have previously taken part in a laboratory-based stress study (confirm with trial site)
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Zoe K Kolokotroni, PhD, Leeds Beckett University
Phone: +441138123271
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Working Memory Performance; Cognitive flexibility and attentional set-shifting.; Sustained attention.; Inhibitory control
Can't join this trial?
Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.