<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Bawa Z</submitter><funding>The Lambert Initiative for Cannabinoid Therapeutics</funding><pagination>e082927</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10966725</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(3)</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>The non-intoxicating plant-derived cannabinoid, cannabidiol (CBD), has demonstrated therapeutic potential in a number of clinical conditions. Most successful clinical trials have used relatively high (≥300 mg) oral doses of CBD. Relatively few studies have investigated the efficacy of lower (&lt;300 mg) oral doses, typical of those available in over-the-counter CBD products.&lt;h4>Methods&lt;/h4>We present a protocol for a randomised, double-blind, placebo-controlled, parallel-group clinical trial investigating the effects of a low oral dose (150 mg) of CBD on acute psychosocial stress, situational anxiety, motion sickness and cybersickness in healthy individuals. Participants (n=74) will receive 150 mg of CBD or a matched placebo 90 min before completing three virtual reality </pubmed_abstract><journal>BMJ open</journal><pubmed_title>Effects of cannabidiol on psychosocial stress, situational anxiety and nausea in a virtual reality environment: a protocol for a single-centre randomised clinical trial.</pubmed_title><pmcid>PMC10966725</pmcid><funding_grant_id>This work was supported by The Lambert Initiative</funding_grant_id><pubmed_authors>McCartney D</pubmed_authors><pubmed_authors>Bedoya-Perez M</pubmed_authors><pubmed_authors>Lau NS</pubmed_authors><pubmed_authors>Bawa Z</pubmed_authors><pubmed_authors>McGregor IS</pubmed_authors><pubmed_authors>Fox R</pubmed_authors><pubmed_authors>MacDougall H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Effects of cannabidiol on psychosocial stress, situational anxiety and nausea in a virtual reality environment: a protocol for a single-centre randomised clinical trial.</name><description>&lt;h4>Introduction&lt;/h4>The non-intoxicating plant-derived cannabinoid, cannabidiol (CBD), has demonstrated therapeutic potential in a number of clinical conditions. Most successful clinical trials have used relatively high (≥300 mg) oral doses of CBD. Relatively few studies have investigated the efficacy of lower (&lt;300 mg) oral doses, typical of those available in over-the-counter CBD products.&lt;h4>Methods&lt;/h4>We present a protocol for a randomised, double-blind, placebo-controlled, parallel-group clinical trial investigating the effects of a low oral dose (150 mg) of CBD on acute psychosocial stress, situational anxiety, motion sickness and cybersickness in healthy individuals. Participants (n=74) will receive 150 mg of CBD or a matched placebo 90 min before completing three virtual reality </description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2026-07-15T15:29:11.003Z</modification><creation>2024-12-03T23:55:46.933Z</creation></dates><accession>S-EPMC10966725</accession><cross_references><pubmed>38531572</pubmed><doi>10.1136/bmjopen-2023-082927</doi></cross_references></HashMap>