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Cannabis UserCANNABEXNCT06081218

Effect of Acute Exercise on Cognitive Functions and Blood Markers of Brain Plasticity in Regular Chronic Cannabis Users

A study testing activity test in people with Cannabis User, run by University Hospital, Lille at 1 site in France.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

The endocannabinoid system (ECS) is a complex endogenous signaling system made up of transmembrane cannabinoid receptors (CB1 and CB2 receptors), their endogenous lipid-derived ligands (the endocannabinoids - eCBs), and enzymes for ligand biosynthesis and degradation. Read more about this study

Who is it for?
Ages 18 to 35 yearsHealthy volunteers can take part
Conditions the study is for
Cannabis User
What is being tested?
activity test
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
60 participants
Where
1 siteFrance
Study dates
7 May 2024to 31 Dec 2029
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 35 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Cannabis consumer group:
  • Cannabis consumption > 100 times in lifetime, last exposure < 7 days, and recent exposure > 10 times in the month.
  • Positive toxicological urine test for ∆-9-THC.
  • Having a cannabis use disorder according to the CAST.
  • Healthy group:
  • Negative urine toxicological test for cannabis.
  • No regular cannabis use for more than 6 months once in a lifetime.
  • No cannabis consumption in the 6 months preceding the study.

Who cannot join

  • For all subjects :
  • Disorders of use of other substances (alcohol, cocaine, opioid, or synthetic drugs).
  • Alcohol consumption greater than 30g per day (averaged over one week) and/or alcohol abuse the week preceding the visit.
  • Under medical treatment.
  • Presence of diagnosed neurological disorders.
  • Diagnosis of a psychotic picture entering axis I, DSM-5.
  • Chronic progressive disease or in remission.
  • Body mass index > 30 kg/m2 (i.e. presence of obesity).

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Olivier Cottencin, MD,PhD contact

0320445962

olivier.cottencin@chru-lille.fr

France1 site, 1 recruiting
  • CHU Lille

    Lille, 59000

    COTTENCIN Olivier, Olivier.COTTENCIN@chu-lille.fr

    GAMELIN François-Xavier, PhD, 06.26.19.23.09, francois-xavier.gamelin@univ-lille.fr

    Recruiting

Other trials in France

About this study

The endocannabinoid system (ECS) is a complex endogenous signaling system made up of transmembrane cannabinoid receptors (CB1 and CB2 receptors), their endogenous lipid-derived ligands (the endocannabinoids - eCBs), and enzymes for ligand biosynthesis and degradation. Interestingly, exercise increase plasma AEA, one of the most famous endocannabinoid. This increase could be involved in exercise-induced neurogenesis and other beneficial exercise adaptations. Chronic cannabis use is associated with alteration of ECS activity. The aim of the study is to compare ECS response to exercise between chronic cannabis users and non-users.

Conditions
Cannabis User
Being tested
activity test

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • activity testOther

    Over 2 weeks, participants have to do a maximal progressive exercise and a 30 min constant exercise at 50% of maximal aerobic power

Study groups in NCT06081218
Study groupRoleWhat they receive
Chronic cannabis usersExperimentalNot described
Receives: Other: activity test
Healthy subjectsSham comparatorNot described
Receives: Other: activity test

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Plasma endocannabinoids levels (pmol/ml)

    Measured: 2 weeks

Secondary outcomes (5)
  1. regulating hormone of endocannabinoids (plasma levels of cortisol, ng/ml)

    Measured: 2 weeks

  2. Blood marker of neurogenesis and neuroplasticity (plasma levels and BDNF, pg/ml)

    Measured: 2 weeks

  3. change in cerebral muscular, oxygenation (HHB), (HbO2), (Hbtot) (arbitrary unit)

    Measured: 2 weeks

  4. Cognitive function (selective attention, stroop test)

    The stroop test can be used to measure a person's selective attention capacity

    Measured: 2 weeks

  5. Oxygen consumption (VO2) (ml/min/kg)

    Measured: 2 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted13 Oct 2023
  2. Study start7 May 2024
  3. Primary completion31 May 2029 (estimated)
  4. Study completion31 Dec 2029 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Non-randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06081218
Sponsor's protocol ID
2016_70
Acronym
CANNABEX
Status last verified
May 2026
First submitted
6 Jul 2023
Last updated
15 May 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing activity test in people with Cannabis User, run by University Hospital, Lille at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 8 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 15 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Olivier Cottencin, MD,PhD (0320445962, olivier.cottencin@chru-lille.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Plasma endocannabinoids levels (pmol/ml) (time frame: 2 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 May 2026.

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