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Cognitive and Cerebral Blood Flow Effects of 2-week Caffeine Abstinence or Maintenance

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Northumbria University

Status

Completed

Conditions

Caffeine Withdrawal
Cognitive Function
Cerebral Haemodynamics
Mood

Treatments

Dietary Supplement: Placebo
Dietary Supplement: Caffeine and Placebo
Dietary Supplement: Placebo and Caffeine
Dietary Supplement: Caffeine

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The purpose of this study is to determine the effects of 2 weeks caffeine abstinence as compared to 2 weeks caffeine maintenance (300mg per day)on cognition and mood. Cerebral blood flow effects will also be assessed in a subset of participants. The role of caffeine abstinence/maintenance in the acute effects of caffeine will also be explored.

Full description

The current randomised, placebo-controlled, double-blind, parallel groups study aims to explore the behavioural effects of 2-weeks caffeine abstinence as well as establishing the role of abstinence in the effects of caffeine administration by administering caffeine or placebo to those in a state of chronic and acute abstinence. This research also aims to explore, in a subset of participants, the cerebral blood flow effects of caffeine abstinence and caffeine administration using Near Infrared Spectroscopy (NIRS). Cerebral blood flow will be measured both at rest and during performance of cognitive tasks.

Enrollment

110 patients

Sex

All

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Male/Female
  • 18 - 40 years
  • Healthy
  • Consume ≥ 150 mg caffeine daily
  • No herbal supplements/prescription medications (excl. contraceptive pill)
  • Non smoker
  • Native English speaker

Exclusion criteria

  • Diagnosis of any significant medical condition or disorder
  • Any known allergy or hypersensitivity to food.
  • BMI >29.9 or <18.5
  • Blood pressure >139/89

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

110 participants in 4 patient groups

Acute withdrawal
Experimental group
Description:
Chronic intervention 100 mg caffeine capsules 3 times per day for 14 days. Acute intervention of placebo capsule on day 15.
Treatment:
Dietary Supplement: Caffeine and Placebo
Acute caffeine-independent of withdrawal
Experimental group
Description:
Chronic intervention of placebo capsules 3 times per day for 14 days. Acute intervention of 100 mg caffeine capsule on day 15.
Treatment:
Dietary Supplement: Placebo and Caffeine
Chronic abstinence
Experimental group
Description:
Chronic intervention of placebo capsules 3 times per day for 14 days. Acute intervention of placebo capsule on day 15.
Treatment:
Dietary Supplement: Placebo
Acute caffeine-in state of withdrawal
Experimental group
Description:
Chronic intervention of 100 mg caffeine capsule 3 times per day for 14 days. Acute intervention of 100 mg caffeine capsule on day 15.
Treatment:
Dietary Supplement: Caffeine

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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