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Cannabigerol Oil for Adolescents With ADHD (CAN-ADHD) (CAN-ADHD)

2026年5月13日 更新者:Rafael Mariano de Bitencourt、Universidade do Sul de Santa Catarina

Potential Effects of Cannabigerol in Adolescents With Attention-Deficit/Hyperactivity Disorder: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial (CAN-ADHD)

This study aims to evaluate the potential effects of full-spectrum cannabigerol (CBG) oil on cognitive and behavioral symptoms in adolescents diagnosed with Attention-Deficit/Hyperactivity Disorder (ADHD). ADHD is a neurodevelopmental disorder characterized by inattention, hyperactivity, and impulsivity, often associated with impairments in academic, social, and emotional functioning.

This is a randomized, double-blind, placebo-controlled clinical trial with a parallel design. A total of 60 adolescents aged 12 to 17 years, diagnosed with ADHD and with insufficient response to previous treatments, will be enrolled and randomly assigned to either the intervention group or the placebo group.

Participants in the intervention group will receive full-spectrum CBG oil (30 mg/mL), administered sublingually, with individualized dosing determined by the study physician and adjusted through weekly monitoring. The placebo group will receive an inert oil matched in appearance and administration conditions.

The intervention will last for 12 weeks, including in-person clinical assessments at baseline, week 6, and week 12, as well as weekly remote monitoring to assess adherence, safety, and dose adjustments.

Primary outcomes will include changes in ADHD symptom severity measured by the SNAP-IV scale. Secondary outcomes will assess quality of life, emotional symptoms, sleep patterns, and safety profile.

This study aims to contribute to the scientific understanding of cannabinoids as a potential therapeutic option for adolescents with ADHD, a population for which current evidence remains limited.

調査の概要

詳細な説明

Attention-Deficit/Hyperactivity Disorder (ADHD) is a neurodevelopmental disorder characterized by persistent symptoms of inattention, hyperactivity, and impulsivity that interfere with academic performance, emotional regulation, social functioning, and quality of life. ADHD is one of the most prevalent neurodevelopmental conditions worldwide and may persist from childhood into adolescence and adulthood. In addition to the core symptoms, individuals with ADHD frequently present emotional dysregulation, sleep disturbances, anxiety symptoms, impaired executive functioning, and psychosocial difficulties that significantly affect both patients and their families.

Current treatment strategies for ADHD include pharmacological and non-pharmacological interventions, with stimulant medications representing the first-line pharmacotherapy in most clinical guidelines. Although these treatments are effective for many patients, a substantial proportion of adolescents experience insufficient clinical response, limited tolerability, adverse effects, or difficulties with long-term adherence. This scenario reinforces the need for investigating alternative and complementary therapeutic approaches capable of targeting both behavioral and emotional dimensions associated with ADHD.

The endocannabinoid system has emerged as a potential target in neuropsychiatric disorders due to its involvement in emotional regulation, cognition, attention, stress response, sleep modulation, and synaptic plasticity. Cannabis-derived compounds have demonstrated neurobiological effects that may influence pathways relevant to ADHD symptomatology. Among these compounds, cannabigerol (CBG) has attracted increasing scientific interest. CBG is a non-intoxicating phytocannabinoid that acts on multiple molecular targets, including cannabinoid receptors, adrenergic pathways, serotonergic signaling, and transient receptor potential channels. Preclinical and observational evidence suggests potential anxiolytic, neuroprotective, anti-inflammatory, and neuromodulatory properties, although controlled clinical evidence remains scarce, particularly in pediatric and adolescent populations.

This study was designed to evaluate the potential effects and safety profile of a full-spectrum cannabigerol-based formulation in adolescents with ADHD. The study consists of a randomized, double-blind, placebo-controlled clinical trial with a parallel-group design. A total of 60 adolescents aged between 12 and 17 years with a previous diagnosis of ADHD will be enrolled and randomly assigned in a 1:1 ratio to either the intervention group or the placebo group.

Participants allocated to the intervention group will receive a full-spectrum Cannabis sativa extract containing cannabigerol (CBG) 30 mg/mL, cannabidiol (CBD) 30 mg/mL, and tetrahydrocannabinol (THC) 3 mg/mL. The formulation will be administered sublingually according to a structured dose titration schedule beginning with low doses and gradually increasing over the first weeks of treatment. From week six onward, dose adjustments may be performed according to clinical response and tolerability, respecting predefined safety limits established in the protocol. Participants allocated to the placebo group will receive a formulation based on medium-chain triglyceride (MCT) oil matched in appearance, color, viscosity, and administration schedule to preserve blinding conditions.

The total intervention period will last 12 weeks. Participants will undergo clinical assessments at baseline, week 6, and week 12. In addition, weekly remote monitoring will be conducted throughout the study to assess treatment adherence, adverse effects, tolerability, and general clinical evolution. Medical follow-up will be performed by trained physicians involved in the research team.

The primary outcome of the study will be the change in ADHD symptom severity assessed through the SNAP-IV (Swanson, Nolan and Pelham Questionnaire, version IV). Secondary outcomes will evaluate quality of life, emotional symptoms, sleep patterns, and safety profile using validated instruments, including the KINDL (Children and Adolescents Quality of Life Questionnaire), WHOQOL-BREF (World Health Organization Quality of Life - Brief Version), DASS-21 (Depression Anxiety and Stress Scale), and CSHQ (Child Sleep Habits Questionnaire).

This study aims to contribute to the advancement of clinical evidence regarding cannabinoid-based interventions in ADHD, particularly involving CBG-rich formulations in adolescents. By using a randomized, double-blind, placebo-controlled design, the study seeks to generate scientifically rigorous data regarding efficacy, tolerability, and safety, potentially supporting future therapeutic strategies and expanding knowledge about the role of the endocannabinoid system in neurodevelopmental disorders.

研究の種類

介入

入学 (推定)

60

段階

  • フェーズ2
  • フェーズ 1

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

  • 名前:Rafael Mariano Bitencourt, PhD
  • 電話番号:+55 48 9 8833-6460
  • メール:bitencourtrm@gmail.com

研究場所

    • Santa Catarina
      • Tubarão、Santa Catarina、ブラジル、88704900
        • 募集
        • Universidade do Sul de Santa Catarina - UNISUL
        • コンタクト:

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 子

健康ボランティアの受け入れ

いいえ

説明

Inclusion Criteria:

  • Adolescents aged 12 to 17 years
  • Diagnosis of Attention-Deficit/Hyperactivity Disorder (ADHD) confirmed using the SNAP-IV (Swanson, Nolan and Pelham Questionnaire, version IV)
  • History of previous treatment with pharmacological or non-pharmacological interventions without significant improvement of symptoms
  • Absence of severe psychiatric disorders or relevant physical comorbidities
  • Ability of the participant and legal guardian to understand study procedures
  • Provision of written informed consent by the legal guardian and assent by the adolescent

Exclusion Criteria:

  • Use of cannabinoid-based substances (natural or synthetic) within 30 days prior to study initiation
  • History of intolerance or adverse reactions to cannabis-derived compounds (e.g., confusion, paranoia, pruritus, excessive drowsiness, vomiting, diarrhea, or seizures)
  • Presence of any significant physical comorbidity
  • Presence of severe psychiatric disorder not related to ADHD
  • Moderate to severe cognitive impairment
  • Inability or unwillingness to complete study procedures or questionnaires adequately

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:ダブル

武器と介入

参加者グループ / アーム
介入・治療
実験的:Full-spectrum CBG oil 30 mg/mL
Participants allocated to this arm will receive sublingual administration of full-spectrum cannabigerol oil for 12 weeks under double-blind conditions. The formulation contains cannabigerol, cannabidiol, and a low concentration of tetrahydrocannabinol. Clinical assessments will be performed at baseline, Week 6, and Week 12, with weekly remote monitoring to evaluate adherence, tolerability, adverse events, and the need for dose adjustments.
Full-spectrum Cannabis sativa extract containing cannabigerol (CBG) 30 mg/mL, cannabidiol (CBD) 30 mg/mL, and tetrahydrocannabinol (THC) 3 mg/mL, administered sublingually for 12 weeks according to a structured dose titration schedule. Treatment will begin with low doses and may be gradually adjusted based on clinical response and tolerability, respecting predefined safety limits established in the study protocol.
プラセボコンパレーター:Placebo (MCT oil)
Participants allocated to this arm will receive sublingual administration of placebo oil for 12 weeks under double-blind conditions. The placebo formulation consists of medium-chain triglyceride (MCT) oil matched to the experimental product in appearance, viscosity, color, and administration schedule. Clinical assessments will be performed at baseline, Week 6, and Week 12, with weekly remote monitoring to evaluate adherence, tolerability, adverse events, and the need for dose adjustments.
Placebo comparator consisting of medium-chain triglyceride (MCT) oil administered sublingually for 12 weeks according to the same dose titration schedule used in the experimental group. The placebo formulation is matched to the active intervention in appearance, color, viscosity, packaging, and administration conditions to maintain blinding throughout the study.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Change in Attention-Deficit/Hyperactivity Disorder symptom severity assessed by the Swanson, Nolan and Pelham Questionnaire, version IV
時間枠:Baseline, Week 6, and Week 12
Evaluation of longitudinal changes in Attention-Deficit/Hyperactivity Disorder symptom severity using the Swanson, Nolan and Pelham Questionnaire, version IV. The Attention-Deficit/Hyperactivity Disorder symptom score includes 18 core items rated from 0 to 3, with total scores ranging from 0 to 54. Higher scores indicate greater symptom severity.
Baseline, Week 6, and Week 12

二次結果の測定

結果測定
メジャーの説明
時間枠
Change in quality of life of legal guardians assessed by the 36-Item Short Form Health Survey
時間枠:Baseline, Week 6, and Week 12
Evaluation of longitudinal changes in legal guardians' quality of life using the 36-Item Short Form Health Survey. Scores are transformed into eight domain scores ranging from 0 to 100, with higher scores indicating better health-related quality of life.
Baseline, Week 6, and Week 12
Change in emotional symptoms assessed by the Depression Anxiety and Stress Scale for Children
時間枠:Baseline, Week 6, and Week 12
Evaluation of longitudinal changes in symptoms of depression, anxiety, and stress using the Depression Anxiety and Stress Scale for Children. Total scores range from 0 to 63, with higher scores indicating greater emotional symptom severity.
Baseline, Week 6, and Week 12
Change in sleep patterns assessed by the Children's Sleep Habits Questionnaire
時間枠:Baseline, Week 6, and Week 12
Evaluation of longitudinal changes in sleep behavior using the Children's Sleep Habits Questionnaire. Total scores range from 33 to 99, with higher scores indicating more sleep problems.
Baseline, Week 6, and Week 12
Number of participants with treatment-related adverse events assessed by the study adverse effects questionnaire
時間枠:Weekly monitoring during 12 weeks and clinical assessments at Baseline, Week 6, and Week 12
Assessment of safety through the number of participants reporting adverse events using the study adverse effects questionnaire. Each adverse event is recorded as present or absent, and severity is classified as mild, moderate, or intense. A higher number of reported adverse events indicates worse tolerability.
Weekly monitoring during 12 weeks and clinical assessments at Baseline, Week 6, and Week 12

その他の成果指標

結果測定
メジャーの説明
時間枠
Number of missed doses reported during weekly remote monitoring
時間枠:Weekly during 12 weeks
Assessment of treatment adherence based on caregiver reports during weekly remote monitoring. The outcome will be reported as the number of missed doses during the 12-week intervention period. A higher number of missed doses indicates lower treatment adherence.
Weekly during 12 weeks
Number of participants requiring dose adjustment during the intervention period
時間枠:Weekly during 12 weeks
Assessment of dose adjustment patterns based on weekly remote monitoring and clinical evaluation. The outcome will be reported as the number of participants requiring dose reduction, delay in titration, or dose increase during the 12-week intervention period.
Weekly during 12 weeks

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年5月1日

一次修了 (推定)

2026年12月18日

研究の完了 (推定)

2026年12月18日

試験登録日

最初に提出

2026年5月6日

QC基準を満たした最初の提出物

2026年5月13日

最初の投稿 (実際)

2026年5月18日

学習記録の更新

投稿された最後の更新 (実際)

2026年5月18日

QC基準を満たした最後の更新が送信されました

2026年5月13日

最終確認日

2026年5月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

未定

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米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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