CClinicalTrials.gg
CompletedNCT06094582CBD-65Updated Dec 22, 2025

Knowledges and Use of Cannabidiol in Older Adults

An observational study in Aging and Frailty, sponsored by University Hospital, Toulouse. Completed at 1 site in France. Open to participants aged 65 Years to 120 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-12-22.

Sponsored by University Hospital, Toulouse · Observational

Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
47
Ages
65 Years to 120 Years
Sex
All
01

Study summary

The use of non-medical cannabidiol (CBD) has been growing recently in France and in the world, in young but also older adults. Few data are available on the use of cannabidiol in older adults. A better knowledge of the use of cannabidiol in older adults, and of their own knowledges of the molecule, is necessary to guide and follow the CBD uptake in this population and avoid potential adverse events.

Read the detailed description

Cannabidiol may be used by patients because it may have beneficial pharmacological effects (including anxiolytic, analgesic, anti-inflammatories or antioxidant effects). Older adults aged 65 years and over, are more frequently at risk of multimorbidity and loss of autonomy, and may present with several symptoms like pain, anxiety, sleep disturbances, that may potentially respond to CBD. The molecule is often marketed as devoid of adverse effects. Nevertheless, with ageing, reduction in liver and kidney function, may have an impact on the metabolism and elimination of CBD and increase the risk of side-effect. As well, the risk of interaction with drugs frequently prescribed in older adults such as CYP3A4 inhibitors (verapamil, ketoconazole …), CYP3A4 inducers (phenytoin, carbamazepine, …) or CY92C19 inhibitors or inducers (fluoxetine …), may increase the risk of side effects. Our hypothesis is that the use of CBD has increased last years in older adults, but that they are insufficiently informed about this molecule. There is a need to assess the prevalence of CBD use in older adults in France, to assess the knowledges of CBD users about this substance, and to better characterize CBD users.

02

Conditions studied

  • Aging
  • Frailty

Browse trials for

Keywords

  • older adults
  • cannabidiol use
  • frailty
03

In context

Frailty

1,198 studies on the registry are indexed under Frailty; 429 are open to participants now.

This study's enrollment of 47 is below the median of 223 across 496 observational studies indexed under Frailty.

Browse Frailty studies →

Lead sponsor

University Hospital, Toulouse is the lead sponsor of 794 studies on the registry; 214 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
65 Years to 120 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

older adults

Inclusion criteria

  • admitted to the frailty clinic, in Toulouse University Hospital during the recruitment period.

Exclusion criteria

Exclusion Criteria:

  • major cognitive disorder with Mini Mental State Examination \<20
  • being under legal supervision or guardianship.
05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
47 participants (actual)
Patient registry
No

Interventions

  • Otherquestionnaire

    Participants will have to fulfill a short questionnaire (10 minutes) concerning their use and knowledges about CBD.

06

What researchers measure

Primary outcomes

  1. Prevalence of CBD use (having consumed CBD at least once)

    The patient will complete a questionnaire about CBD use

    Time frame: 1 day

07

Study locations

1 site
  • University Hospital Toulouse
    Toulouse, 31059, France
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 22, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06094582
Lead sponsor
University Hospital, Toulouse
Responsible party
Sponsor
First posted
Oct 23, 2023
Start date
Oct 26, 2023
Primary completion
Dec 26, 2023
Completion
Dec 26, 2023
Last update
Dec 22, 2025

Study contacts

Sandrine SOURDET, MD
principal investigator · University Hospital, Toulouse

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion