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

13. Mai 2026 aktualisiert von: 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.

Studienübersicht

Detaillierte Beschreibung

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.

Studientyp

Interventionell

Einschreibung (Geschätzt)

60

Phase

  • Phase 2
  • Phase 1

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Studienorte

    • Santa Catarina
      • Tubarão, Santa Catarina, Brasilien, 88704900
        • Rekrutierung
        • Universidade do Sul de Santa Catarina - UNISUL
        • Kontakt:

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Kind

Akzeptiert gesunde Freiwillige

Nein

Beschreibung

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

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Doppelt

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: 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.
Placebo-Komparator: 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.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Change in Attention-Deficit/Hyperactivity Disorder symptom severity assessed by the Swanson, Nolan and Pelham Questionnaire, version IV
Zeitfenster: 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

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Change in quality of life of legal guardians assessed by the 36-Item Short Form Health Survey
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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

Andere Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Number of missed doses reported during weekly remote monitoring
Zeitfenster: 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
Zeitfenster: 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

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

1. Mai 2026

Primärer Abschluss (Geschätzt)

18. Dezember 2026

Studienabschluss (Geschätzt)

18. Dezember 2026

Studienanmeldedaten

Zuerst eingereicht

6. Mai 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

13. Mai 2026

Zuerst gepostet (Tatsächlich)

18. Mai 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

18. Mai 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

13. Mai 2026

Zuletzt verifiziert

1. Mai 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Plan für individuelle Teilnehmerdaten (IPD)

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UNENTSCHIEDEN

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

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