Skip to main content
Journal of Cannabis Research logoLink to Journal of Cannabis Research
. 2025 Oct 15;7:77. doi: 10.1186/s42238-025-00341-4

Beyond the hype - who uses cannabidiol for self-medication – and why: a cross-sectional study in Germany

Eva-Maria Krowartz 1,2,, Carlotta Riemerschmid 1,2, Stefanie J Klug 3, Luana F Tanaka 3,4, Eva-Hoch 1,2,5
PMCID: PMC12529850  PMID: 41094600

Abstract

Introduction

Cannabidiol (CBD) products are increasingly popular, marketed with health claims despite limited clinical evidence. This study investigates motives for CBD use in self-medication and explores sociodemographic characteristics and consumption patterns among regular users (at least monthly).

Methods

Cross-sectional data were collected via an online survey (January 15–March 15, 2023) in Germany using convenience sampling. Associations between the motive of use (self-medication vs. recreational), sociodemographic characteristics, and consumption patterns were assessed using cross-tabulations, with Chi-square tests () and Cramér’s V (V) for effect sizes. Self-medication predictors were analyzed using logistic regression, reporting adjusted odds ratios (aOR) and confidence intervals (CI).

Results

A total of 730 participants participated in the study, with 702 (96.2%) complete cases included in the final analysis. The sample comprised 78.8% males with a mean age of 34.9 years (mean SD: 11.4). Among those using CBD primary for self-medication (37.9%, n = 266), the most prevalent motives were sleeping problems (52.3%), chronic pain (47.4%), depression (45.5%), and anxiety (44.4%). Motives for use were significantly associated with gender (=18.4, V = 0.162, p < .001), age (=42.3, V = 0.246, p < .001) and occupation (=51.8, V = 0.272, p < .001). In the adjusted logistic regression, older individuals (40–49 years, aOR: 1.97, CI: 1.05–3.70, p = .035; ≥50 years, aOR: 2.81, CI: 1.36–5.83, p = .005) and those unemployed or retired (aOR: 3.55, CI: 2.13–5.92, p < .001) were more likely to use CBD for self-medication. Higher chances were also observed in once-daily users (aOR: 2.52, CI:1.23–5.13, p = .011), those consuming CBD morning and evening (aOR: 3.05, CI: 1.42–6.56, p = .004), and individuals using it when needed (aOR: 2.72, CI: 1.72–4.29, p < .001). Smoking CBD mixed with tobacco (aOR: 0.37, CI: 0.22–0.62, p < .001) or pure CBD (aOR: 0.55, CI: 0.30–0.99, p = .046) was negatively associated with self-medication.

Conclusion

This study identifies motives for CBD use in self-medication and examines associations with sociodemographic characteristics and consumption patterns. Clinical trials are needed to confirm efficacy, focusing on dose-response, administration and drug interactions. In the interest of users, the legal status—especially considering the recent partial legalization—should be clearly defined.

Keywords: Cannabidiol, CBD, Self-Medication, Cannabis, Partial legalization

Introduction

Cannabis Sativahas been utilized for medicinal, ritualistic, and recreational purposes for millennia (Russo 2007).The plant contains naturally occurring phytocannabinoids, which are key contributors to its pharmacological effects (Reekie et al. 2017). Cannabidiol (CBD), a phytocannabinoid synthesized via the secondary metabolism ofCannabis sativa(Pisanti et al. 2017), differs from tetrahydrocannabinol (THC), the most prominent cannabinoid, in that it does not activate cannabinoid-1-receptors. These receptors are primarily expressed in the brain and mediate the psychotropic effects commonly associated with cannabis consumption (Dingermann 2021).

In Germany, the lifetime prevalence of CBD use ranges from 4.3% (Alayli et al. 2022)to 11.4% (Geppert et al. 2020)in 2020, with CBD products gaining increasing popularity (Manthey 2023). CBD is primarily sold as dried flowers or as isolated CBD, which is processed into oil or incorporated into food and beverages. In Germany, the legal status of CBD products is complex und constantly changing (Kirsch 2023). Initially, the classification of CBD as a narcotic was evaluated. CBD dried flowers were considered narcotic substances due to their residual THC content and the possibility of misuse. Dried plant material often retains traces of THC above the legal threshold of 0.2% THC (Wissenschaftliche 2020). Courts contended that the potential for intoxication exists, thereby making the sale illegal, despite the economical impracticability due to the large amounts of dried flowers needed (Kirsch 2023). Following the partial legalization of recreational cannabis in April 2024, the legal status of CBD dried flowers in Germany has been redefined. The new legislation permits the sale of CBD dried flowers, provided they are derived from approved industrial hemp strains and do not exceed the newly defined THC limit of 0.3% (Beckmann 2024).

Other CBD-containing products, such as high-dose CBD oils with isolated CBD that may have pharmacological effects or are intended for disease treatment, are classified as medicinal products within the European Union (EU). These products must receive authorization in accordance with EU pharmaceutical regulations (European 2001). The therapeutic potential and potential adverse health effects of CBD have been widely debated, preclinical studies suggest that CBD interacts with various molecular targets, including receptors, enzymes, and ion channels, indicating potential therapeutic applications (Ibeas Bih et al. 2015). Nevertheless, large-scale randomized-controlled trials (RCTs) in humans remain limited (Britch et al. 2021; Ibeas Bih et al. 2015), and to date, the only approved medication containing the active ingredient CBD isEpidyolex, which received approval in September 2019 for the treatment of treatment-resistant epilepsy in Dravet syndrome, Lennox-Gastaut syndrome and tuberous sclerosis complex (Devinsky et al. 2017, 2016; GW 2021; Thiele et al. 2021, 2018).

In contrast, low-dose CBD products, such as food products, that are not intended for medicinal purposes are not regulated as pharmaceuticals (Lachenmeier 2019). Given that CBD alone does not exhibit psychoactive effects and is not considered an addictive substance, the European Commission concluded on December 3, 2020, that CBD should be classified as a novel food underRegulation (EU) No. 2015/2283(Lachenmeier 2020). Novel foods must undergo authorization by the European Food Safety Authority (EFSA). In 2022, the EFSA published a statement concluding that the safety of CBD as a novel food could not be determined due to existing uncertainties and data gaps (Nutrition et al. 2022). The Federal Office of Consumer Protection and Food Safety therefore concludes that CBD in food products, including dietary supplements, is currently not authorized for sale (6undefined ). Although considerable uncertainties remain regarding the regulatory status of CBD, Germany is expected to experience a significant increase in revenue within the CBD products market, with projections indicating a rise of 0.8% to approximately €395,41 million by 2025. When compared globally, Germany ranked second in 2024, following the United States (U.S), in terms of revenue generated from CBD retail sales (Statista 2024).

Due to the constantly changing and unclear legal status, unregulated over-the-counter CBD products are available in retail stores and online (McGregor et al. 2020), often being marketed illegally with unverified health claims (Engeli et al. 2025). Currently, no prevention campaigns specifically target misinformation about CBD products. While German consumer associations provide guidance (Verbraucherzentrale. 2025, 2023; Verbraucherzentrale 2024, 2019), manufacturers’ commercial interests often conflict with users’ interests. The ambiguous and evolving classification of CBD creates loopholes that producers repeatedly exploit to market their products with unverified claims (Melchert et al. 2024). Advertising, predominantly distributed via social media, primarily promotes CBD for pain, anxiety disorders, sleep disorders, and stress (Soleymanpour et al. 2021). Those advertised health claims are also reflected in users’ motivations for use. Self-medication has been reported for a variety of medical and psychological conditions. Cross-sectional studies in France (Fortin et al. 2021), the United Kingdom (UK) (Moltke and Hindocha 2021), the U.S (Corroon and Phillips 2018)., Germany (Geppert et al. 2020)and Poland (Binkowska et al. 2024)indicate that CBD is frequently used as a self-administered treatment for conditions such as stress, sleep disorders, pain, and mental health issues, including depression and anxiety (Binkowska et al. 2024; Corroon and Phillips 2018; Fortin et al. 2021; Geppert et al. 2020; Moltke and Hindocha 2021). Although CBD is widely available and frequently marketed for its health benefits, its use is not without potential risks. While large-scale human safety data remain limited, emerging evidence suggests a potential association between CBD use and increased rates of adverse events, including hepatotoxicity (Moore et al. 2024).

Given the potential risks associated with unregulated CBD products, the increasing demand, and recent regulatory changes following partial legalization, this study provides an exploratory analysis of regular German CBD users. Previous cross-sectional studies provide only limited empirical evidence on the sociodemographic characteristics and consumption patterns of regular users who primarily utilize CBD for self-medication. This study investigates the motives for CBD self-medication in a sample of regular users and examines sociodemographic factors and consumption patterns associated with self-medication.

Methods

Study design

The online survey was conducted from January 15 to March 15, 2023, using LimeSurvey (LimeSurvey GmbH) and employed convenience sampling to recruit regular CBD users in Germany. At the beginning of the questionnaire, participants provided informed consent for the use of their data for the specified research purposes. No personal data were collected, and participation was voluntary without the provision of incentives. The study sample comprised adult, self-selected CBD users in Germany who accessed the survey via a direct link or QR code. The inclusion criteria encompassed regular CBD consumption (at least monthly), residency in Germany, proficiency in German, and internet access to complete the survey. Regular CBD consumption and residency were verified using filter questions. Participants who did not meet the inclusion criteria received a notification of their ineligibility, and the questionnaire was subsequently terminated with a closing message. Recruitment was facilitated by CBD retailers and the German Hemp Association (DHV), who distributed the survey through platforms, such as YouTube, Instagram, and email newsletters. CBD retailers were identified via Google and were contacted to request their assistance in disseminating the survey through their channels. A search identified 84 retailers that were initially contacted by email. The overall response rate among CBD retailers was 57.1%, with 28 retailers (33.3%) in total supporting the recruitment process.

Measurement

The questionnaire was based on that of Moltke et al. (Moltke and Hindocha 2021), translated into German, and adapted to the German population where applicable. It consisted of 23 questions and an additional open-ended item for further remarks. The questions were organized into three main domains: socioeconomic characteristics, motives for use, and patterns, and self-perceived effectiveness, safety, and acquisition. Methodological feedback was provided by the IFT Institut für Therapieforschung, Center for Mental Health & Addiction Research, while content-related insights were obtained from CBD retailers.

Outcome

The main outcome was primary use motive, dichotomized into recreational use and self-medication. Participants selected either “For medical reasons (to treat at least one illness or symptom)” (self-medication) or “For general health and well-being” (recreational use). Based on their response, the subsequent question presented a predefined list of either recreational or self-medication motives, with multiple responses allowed. Self-perceived effectiveness was assessed among participants who reported self-medication as their primary use motive. Sociodemographic characteristics assessed included gender, age, education, and occupation, with single responses required. Regarding consumption patterns, participants were asked to report the frequency, route of administration, time of consumption, duration of use, and the amount consumed per day. For each item, predefined response categories were provided, with participants instructed to select one single category that most accurately reflected their behavior.

Statistical analysis

Although vocational qualification was assessed, it was excluded from further analysis due to high multicollinearity with education and occupation, a factor crucial for regression modeling (Kim 2019). To ensure an adequate number of observations per category, particularly for regression modeling, some categories were collapsed. Participants who reported a non-binary gender were recoded as missing due to a low number of observations in this category. Education was recoded into three categories: ‘high school diploma or equivalent qualification’, ‘upper secondary education’, and ‘lower secondary education or below’. Occupation was recoded into the following categories: ‘employed full-time’, ‘employed part-time’, ‘pupil/student/intern or marginally employed’, and ‘not currently employed or retired’. Regarding the preferred route of administration, categories such as ‘as a drink’, ‘as an oral spray’, ‘as food’, ‘in a pipe’, ‘in a hookah’, ‘capsules or pills’, and ‘topically, on the skin’ were merged into the category ‘other’.

Cross-tabulations were performed to examine the association between motive of use, sociodemographic characteristics, and consumption patterns. Chi-squared () tests assessed relationships, with Cramér’s V (V) used to measure effect size. Vwas applied to determine the strength of association between two nominally scaled variables, with values between 0.1 and 0.3 indicating a weak association, 0.4 to 0.5 indicating a moderate association, and values greater than 0.5 indicating a strong association (Cohen 1988). Binary logistic regressions were performed to assess associations between sociodemographic characteristics, consumption patterns, and the likelihood of reporting self-medication as the primary motive for CBD use (reference: recreational use), while controlling for other factors. To quantify the strength of associations and assess statistical significance, adjusted odds ratios (aORs) with 95% confidence intervals (CI) are reported. Variables that showed a significant association with motive of use, as identified byV and corresponding p-values (p), were included in the model. These predictors included gender, age, occupation, frequency and time of consumption, and route of administration. Overall model significance was tested using a statistic, which compares the null model (without predictors) to the model with predictors. The statistic is calculated by evaluating the difference between the observed and expected outcomes for each participant (Harris 2021).

Results

In total, 730 individuals aged 18 to 80 fully completed the survey and received a completion message, after which the survey was terminated; these participants were considered valid cases. Participants with missing values in any of the variables under investigation were excluded, resulting in a final analytical sample of n = 702. Data analysis was performed using Stata (version 15.1). The sample consisted of 78.8% male users, with a mean age of 34.9 years (range: 18–80 years, mean standard deviation: 11.4). A detailed overview of sociodemographic characteristics and consumption patterns for the whole sample is provided in Table 1.

Table 1.

Sociodemographic characteristics and consumption patterns in a self-selected sample of regular German CBD users (n = 702)

Total sample (n = 702)
n %
Gender
 Male 553 78.8
 Female 149 21.2
Age groups (years)
 18–24 129 18.4
 25–29 150 21.4
 30–39 221 31.5
 40–49 124 17.7
 ≥ 50 78 11.1
Education
 High school diploma 355 50.6
 Upper secondary education 245 34.9
 Lower secondary education or below 102 14.5
Occupation
 Employed full-time 412 58.7
 Employed part-time 88 12.5
 Pupil/student/intern or marginally employed 91 13.0
 Not currently employed or retired 111 15.8
Frequency of use
 At least monthly 83 11.8
 At least weekly 82 11.7
 Several times per week 175 24.9
 Once a day 133 19.0
 Several times per day 229 32.6
Route of administration
 Sublingually 159 22.7
 Smoking (with tobacco) 216 30.8
 Smoking (pure) 121 17.2
 Vaping 124 17.7
 Other 82 11.7
Daytime of consumption
 In the evening 310 44.2
 In the morning 21 3.0
 Morning and evening 52 7.4
 Multiple times per day 144 20.5
 When needed 175 24.9
Consumption duration (years)
 < 1 95 13.5
 1–2 190 27.1
 2–5 297 42.3
 > 5 120 17.1
Amount consumed per day (mg)
 < 100 197 28.1
 100–300 142 20.2
 > 300 91 13.0
 Do not know 272 38.8

Around one third of the sample (37.9%, n = 266) reported using CBD primary for self-medication. A weak association between motive of use and sociodemographic factors, as indicated by V, was found for gender, age group, and occupation, while no significant association was observed for education. Male gender was associated with recreational CBD use, while female users were more likely to use CBD for self-medication. (=18.4, V = 0.162, p <.001). Additionally, a weak association was found between age group and motive of use (=42.3, V = 0.246, p <.001), with increasing age being associated with self-medication. Furthermore, motive of use was significantly associated with occupation (=51.8, V = 0.272, p <.001). A higher proportion of full-time employed participants were found among recreational users (65.4% vs. 47.7%), while individuals not currently employed or retired reported using CBD primarily for self-medication more frequently (28.2% vs. 8.3%). No significant association was observed between education and motive of use (=5.7, V = 0.090, p =.058). Regarding consumption patterns, V indicated significant associations between motive of use and specific consumption patterns. Motive of use was associated with frequency of use (=28.5, V = 0.202, p <.001), route of administration (=51.7, V = 0.271, p <.001), and the daytime of consumption (=45.5, V = 0.256, p <.001), all of which indicated weak effect sizes. In contrast, no significant associations were found between motive of use and consumption duration (=5.4, V = 0.088, p =.147), or the amount consumed per day (=3.6, V = 0.071, p =.311).

Sociodemographic characteristics and consumption patterns, stratified by primary consumption motive, are presented in Table 2, along with V and p to assess the magnitude and significance of differences.

Table 2.

Sociodemographic characteristics and consumption patterns of regular cannabidiol users in Germany by primary use motive

Self-medication (n = 266) Recreational use (n = 436) V 1) p
n % n %
Gender 0.162 < 0.001*
 Male 187 70.3 366 83.9
 Female 79 29.7 70 16.1
Age Groups (years) 0.246 < 0.001*
 18–24 29 10.9 100 22.9
 25–29 48 18.1 102 23.4
 30–39 81 30.5 140 32.1
 40–49 58 21.8 66 15.1
 ≥ 50 50 18.8 28 6.4
Education 0.090 0.058
 High school diploma 122 45.9 233 53.4
 Upper secondary education 96 36.1 149 34.2
 Lower secondary education or below 48 18.1 54 12.4
Occupation 0.272 < 0.001*
 Employed full-time 127 47.7 285 65.4
 Employed part-time 35 13.2 53 12.2
 Pupil/student/intern or marginally employed 29 10.9 62 14.2
 Not currently employed or retired 75 28.2 36 8.3
Frequency of use 0.202 < 0.001*
 At least monthly 21 7.9 62 14.2
 At least weekly 23 8.7 59 13.5
 Several times per week 51 19.2 124 28.4
 Once a day 60 22.6 73 16.7
 Several times per day 111 41.7 118 27.1
Route of administration 0.271 < 0.001*
 Sublingually 83 31.2 76 17.4
 Smoking (with tobacco) 52 19.6 164 37.6
 Smoking (pure) 30 11.3 91 20.9
 Vaping 58 21.8 66 15.1
 Other 43 16.2 39 8.9
Daytime of consumption 0.256 < 0.001*
 In the evening 78 29.3 232 53.2
 In the morning 12 4.5 9 2.1
 Morning and evening 32 12.0 20 4.6
 Multiple times per day 60 22.6 84 19.3
 When needed 84 31.6 91 20.9
Consumption duration (years) 0.088 0.147
 < 1 35 13.2 60 13.8
 1–2 60 22.6 130 29.8
 2–5 119 44.7 178 40.8
 > 5 52 19.6 68 15.6
Amount consumed per day (mg) 0.071 0.311
 < 100 83 31.2 114 26.2
 100–300 56 21.1 86 19.7
 > 300 35 13.2 56 12.8
 Do not know 92 34.6 180 41.3

* Significant on a threshold of α < 0.05

1) Cramér’s V: Strength of association between categorical variables (0 = no association, 1 = strong association)

Among individuals that reported using CBD primary for self-medication, users treated on average 3 to 4 different medical conditions with CBD (mean: 3,7). More than half of the primary medical users reported that they treated insomnia or other sleeping problems (52.3%), chronic pain (47.4%), depression (45.5%), or anxiety (44.4%) with CBD. The most common indications for primary medical CBD use are displayed in (Fig. 1).

Fig. 1.

Fig. 1

Reasons for self-medication among self-selected regular CBD users in Germany (multiple responses allowed) (n = 266). 1) Substance not specified. Note: ADHD, attention deficit disorder; CBD, cannabidiol; COPD, chronic obstructive pulmonary disease; PTST, post-traumatic-stress disorder

Among participants who reported self-medication as their primary motive for CBD use (n = 266), the perceived effectiveness of CBD varied. A small proportion (3.8%, n = 10) indicated that CBD was not effective for the treatment of their illness or symptoms. About one-third of participants (32.3%, n = 86) reported that CBD was helpful in combination with other medications. Similarly, 31.6% (n = 84) stated that CBD alone was moderately to well effective, while 32.3% (n = 86) rated CBD alone as very effective. (Fig. 2) illustrates the perceived effectiveness of CBD among participants using it primarily for self-medication.

Fig. 2.

Fig. 2

Perceived effectiveness of CBD among users with self-medication as primary motive (single response; n = 266)

The regression model assessing self-medication as the primary motive for CBD use included variables significantly associated with the motive, as indicated by V and p. Predictors in the model were gender, age, occupation, route of administration, frequency, and time of consumption. Education, consumption duration and daily amount were excluded due to non-significant associations. After excluding vocational qualification, no significant multicollinearity was detected among the variables (variance inflation factor [VIF] = 1.88). The overall model was significant (likelihood ratio (Lachenmeier 2020) = 153.21,p <.001), suggesting that at least some of the predictors significantly influenced the dependent variable.

After adjusting for covariates in the logistic model, gender (aOR: 1.50, CI: 0.96–2.33, p =.074) was no longer significantly associated with use motive. Age categories revealed that older individuals, had significantly higher odds of using CBD for medical purposes among older individuals, aged 40–49 (aOR: 1.97, CI: 1.05–3.70, p =.035), with the highest chance observed for those aged 50 and above (aOR: 2.81, CI: 1.36–5.83, p =.005). Occupation was also a significant predictor, with individuals who were not currently employed or retired showed significantly higher odds of using CBD for self-medication (aOR: 3.55, CI: 2.13–5.92, p <.001), compared to full-time employees. Regarding the form of consumption, smoking CBD mixed with tobacco and smoking pure CBD were both negatively associated with medical use, compared to sublingual ingestion. Specifically, the odds of using CBD for medical purposes were lower for those smoking CBD mixed with tobacco (aOR: 0.37, CI: 0.22–0.62, p <.001) and for those smoking pure CBD (aOR: 0.55, CI: 0.30–0.99, p =.046). In terms of frequency of use, CBD users who consumed CBD once a day had significantly higher odds of using CBD for medical reasons compared to those using it at least monthly (aOR: 2.52, CI: 1.23–5.13, p =.011). Additionally, individuals who used CBD multiple times a day showed increased odds of using it for medical reasons, though this was not statistically significant (aOR: 1.60, CI: 0.87–2.96, p =.132). Furthermore, consumption on an as-needed basis was significantly associated with increased odds of using CBD primarily for self-medication (aOR: 2.72, CI: 1.72–4.29, p <.001), as was morning and evening use (aOR: 3.05, CI: 1.42–6.56, p =.004), compared to users who reported using CBD only in the evening. Table 3 presents the final model.

Table 3.

Binary logistic regression predicting self-medication (reference: recreational use) with CBD by sociodemographics and consumption patterns

aOR 1) 95%-CI 2) p
Gender
 Male [Reference]
 Female 1.50 0.96–2.33 0.074
Age groups (years)
 18–24 [Reference]
 25–29 1.65 0.92–2.95 0.095
 30–39 1.57 0.89–2.75 0.117
 40–49 1.97 1.05–3.70 0.035*
 ≥ 50 2.81 1.36–5.83 0.005*
Occupation
 Employed full-time [Reference]
 Employed part-time 1.12 0.64–1.94 0.695
 Pupil/student/intern or marginally employed 1.46 0.84–2.56 0.182
 Not currently employed or retired 3.55 2.13–5.92 < 0.001*
Frequency of use
 At least monthly [Reference]
 At least weekly 1.50 0.70–3.22 0.296
 Several times per week 1.08 0.56–2.09 0.813
 Once a day 2.52 1.23–5.13 0.011*
 Several times per day 2.00 0.98–4.08 0.057
Route of administration
 Sublingually [Reference]
 Smoking (with tobacco) 0.37 0.22–0.62 < 0.001*
 Smoking (pure) 0.55 0.30–0.99 0.046*
 Vaping 1.18 0.69–2.04 0.549
 Other 0.92 0.51–1.68 0.790
Daytime of consumption
 In the evening [Reference]
 In the morning 1.59 0.57–4.45 0.375
 Morning and evening 3.05 1.42–6.56 0.004*
 Multiple times per day 1.60 0.87–2.96 0.132
 When needed 2.72 1.72–4.29 < 0.001*

* Significant on a threshold of α < 0.05

1) Adjusted odds ratio (aOR)

2) Confidence interval (CI)

Discussion

The present study examined associations between user the primary motive of use, demographic characteristics as well as consumption patterns in a sample of German CBD users. Primary consumption motive was associated with gender, age group, occupation, frequency, route of administration and daytime of consumption. In the adjusted model, consumption patterns, age and occupation remained statistically associated with motive of use; with older users and those who reported being currently unemployed or retired having higher chances of reporting CBD for self-medication. Additionally, the results indicated that daily and as-needed CBD consumption, as well as morning and evening use, were associated with increased odds of self-medication as the primary motive. In contrast, smoking CBD (both mixed with tobacco and pure) was associated with decreased odds of self-medication. Among an adult German sample of regular CBD users, the most frequently reported motives for self-medication were sleeping problems, chronic pain, depression and anxiety. Evidence indicates that cannabis products are often used as a ‘natural’ alternative when conventional treatments have proven ineffective and because they are perceived as preferable to conventional medications, offering natural relief without the intoxicating effects associated with THC-containing products (VanDolah et al. 2019; Wallace et al. 2020). Such expectancies, combined with misleading advertising in the media (Engeli et al. 2025; Moore et al. 2024), may contribute to the use of CBD for self-medication across a wide range of conditions. This may also lead to an overestimation of therapeutic effectiveness, which seems to be reflected in our data, as only a small proportion of participants reported that CBD was not helpful for managing their medical conditions.

Self-medication with CBD: demographic characteristics and consumption patterns

Consistent with previous findings from the UK and Canada (Goodman et al. 2022; Moltke and Hindocha 2021), women were more likely to consume CBD for self-medication. The gender-related effects may be attributable to the fact that several conditions frequently managed with CBD, as well —such as (premenstrual) pain, anxiety, and depression—are either unique to or more prevalent among women, as previously hypothesized by Goodman and colleagues (Goodman et al. 2022). After adjusting for other predictors, the gender effect was no longer statistically significant. Findings from this sample indicate that consumption patterns, as well as age and occupation, may be a stronger and more reliable predictor than gender. After adjusting for other factors, older age remained positively associated with medical consumption motives, with adults aged 40 and older more likely to use CBD for medical motives, a finding consistent with the results of Geppert et al. (Geppert et al. 2020). Additionally, being unemployed or retired was also associated with primary medical use. These associations may be mediated by a higher burden of disease in older subgroups, indicating that age presents a strong confounder. Primary recreational CBD use was positively associated with administration via smoking (with or without tobacco), while the opposite applied for the consumption for self-medication. The detrimental effects of smoking—especially with tobacco—are associated with various negative health outcomes (U.S. 2024), which might contradict health-conscious decisions. Those findings were consistent with results from Goodmann and colleagues (Goodman et al. 2022), indicating that CBD oil, which is used sublingually is rather used for self-medication, compared to other application forms. Recreational CBD use was mostly consumed in the evening, which indicates that it is predominantly used for relaxation during free. In contrast, medical use was consumed when needed or at a specific time which aligns more closely with conventional medication usage. Additionally, primarily use for self-medication was associated with a higher consumption frequency, which also aligns more closely with conventional medication use.

Self-medication with CBD: findings from other countries

Approximately one-third of the present sample used CBD primary for self-medication, while the majority reported using CBD primarily for recreational purposes. These findings are in line with data from France, where treatment of disease only represented the main motivation in one in four cases (Fortin et al. 2021). In contrast, in the U.S., two in three users reported that they used CBD for the treatment of a medical condition (Corroon and Phillips 2018). Evidence suggests country-specific differences in the motive of use and perception of CBD products. Findings indicate that CBD tends to be regarded more as a recreational product in Germany and France, while in the U.S. and the UK it seems to be more frequently used in the context of self-medication. Differences in perception and consumption of CBD products might be driven by national law enforcement policies regarding cannabis. Indeed, comparisons of user motivations and patterns across the EU, U.S., and UK indicate that regulatory frameworks are pivotal in shaping variations in user behaviors (Fortin et al. 2021; Mead 2017). In the U.S., the legalization of cannabis in several states has facilitated greater acceptance of CBD as a medical product and was associated with more favorable health perceptions regarding cannabis consumption (Gali et al. 2021). For instance, the consumption and sale of CBD flowers is more strictly prosecuted in the UK than in Germany or France (Hurt 2023). The dried plants, which is often administered via smoking and associated with recreational use, has high user rates in Germany and France, which potentially underscore the significant influence of legal frameworks on user access and perceptions of CBD products. In conclusion, differences in CBD use motives may exist between countries with varying cannabis and CBD regulations, possibly reflecting differing perceptions of CBD. This is particularly relevant for Germany, where recent cannabis legalization is expected to increase the availability and use of cannabis products, including CBD (Cerdá et al. 2008; Mennis et al. 2023). Future research should examine how regulatory frameworks shape perceptions and consumption motives of CBD, using representative samples to enable valid cross-country comparisons. Surveys should therefore investigate associations between use motives, consumption patterns, and regulatory contexts for medical and recreational cannabis, as well as capture the extent to which cannabis products—particularly cannabidiol—may be advertised in different countries and assess user expectations accordingly.

CBD for sleep, pain, and depression and anxiety: evidence of effectiveness

The reported medical indications for CBD use align with studies from other countries, which also report anticipated health benefits such as sleep improvement, pain relief, and relief from depression or anxiety (Alayli et al. 2022; Binkowska et al. 2024; Corroon and Phillips 2018; Fortin et al. 2021; Geppert et al. 2020; Goodman et al. 2022; Moltke and Hindocha 2021). There is limited evidence supporting the efficacy of CBD in treating these conditions. A possible explanation for perceived benefits could be the placebo effect, reinforced by non-evidence-based health claims promoted by media and retailers (Moore et al. 2024). Laboratory and animal studies indicate an effect of CBD on the circadian system (Chagas et al. 2013; Ibeas Bih et al. 2015; Leweke et al. 2012; Silvestro et al. 2020; Suraev et al. 2020). Human trials suggest CBD may improve sleep by alleviating symptoms of conditions like pain or anxiety (Notcutt et al. 2004), but its direct impact on the circadian system is still unclear. Placebo effects may largely explain perceived sleep benefits, as a controlled trial by Linares et al. (Linares et al. 2018)showed no acute effect on the sleep-wake cycle. Results from preclinical studies suggest that CBD may alleviate pain by enhancing N-arachidonoylethanolamine signaling, an endocannabinoid involved in pain modulation (Costa et al. 2004; Ibeas Bih et al. 2015). Animal studies have reported a reduction in pain-like behaviors (Soliman et al. 2021). However, reviews on cannabis-based treatments often focus on THC-CBD combinations, complicating the attribution of analgesic effects specifically to CBD alone (Boyaji et al. 2020). In most randomized controlled trials, isolated CBD has shown limited efficacy in pain reduction (Moore et al. 2024). In preclinical studies and animal models, CBD has been shown to interact with the same serotonin receptors that are associated with depression and anxiety (Crippa et al. 2011; Fakhfouri et al. 2019; García-Gutiérrez et al. 2020; Iannotti and Vitale 2021; Ibeas Bih et al. 2015; Moore et al. 2024; Silvestro et al. 2020). This interaction may contribute to its potential therapeutic effects on mood disorders. Although human trials have reported reduced anxiety in patients with anxiety disorders (Bergamaschi et al. 2011; Crippa et al. 2011), recent findings by Gournay et al. (Gournay et al. 2024)suggest that strong user expectations regarding CBD’s anxiety-reducing effects contribute to its perceived effectiveness. Existing studies show heterogeneity in study settings, underscoring the need for research on dose-response, treatment timelines, and administration methods. CBD’s effects vary by dosage, strain, treatment duration, and administration route, with many studies limited by small sample sizes. While molecular properties and animal studies support its therapeutic potential, further clinical investigation is needed to establish efficacy in humans, beyond the placebo effect (Moore et al. 2024). In addition, Given CBD’s potential to interact with other medications (Brown and Winterstein 2019) and induce adverse effects, further investigation into drug-CBD interactions is essential to assess their clinical significance and associated risks.

Strengths and limitations

This study is the first to identify consumption patterns associated with different use motivations among regular CBD users. The consistency of the findings related to user motivations with previous cross-sectional studies from France, the UK, and the US, strengthens the generalizability of the results. The present study comes along several limitations. First, the study is subject to selection bias due to self-sampling. Individuals with negative experiences regarding their CBD use may be underrepresented, while those more favorable toward CBD products are more likely to participate. This could result in an overestimation of the self-perceived therapeutic effectiveness. Due to the recruitment method of convenience sampling, we do not claim representativeness of the sample. Other limitations involve reliance on retrospective self-reporting, lack of objective measures, and the inability to establish causality due to the cross-sectional design. Reliance on non-validated questionnaires is a limitation, highlighting the need for CBD-specific instruments, as THC-related questionnaires may not adequately capture CBD-specific outcomes. At present, only the Cannabidiol Outcome Expectancies Questionnaire (CBD-OEQ)is validated (Walukevich-Dienst et al. 2022), but it measures psychometric properties, such as expectancies and endorsement, rather than motives or consumption patterns. With regard to validated questionnaires, future studies should include additional confounders, as the regression model explained only around 16% of the variance. Relevant factors include comorbidities and physician-diagnosed chronic conditions, rather than relying solely on self-reported medical indications, which do not constitute a medical diagnosis. Moreover, the use of other substances such as THC or tobacco should be assessed, as they may constitute important confounders. In addition, the response option‘addiction cessation’ in the predefined list of medical indications should be specified more precisely to enable a more accurate investigation of associations between CBD use and other substances. These methodological shortcomings of the survey instrument highlight the need for validated CBD-specific outcome measures. In addition, the lack of distinction between CBD and THC users may have confounded the observed therapeutic effects.

Conclusion

This study represents the first in depth-analysis of sociodemographic characteristics and consumption patterns among individuals who primarily use CBD for self-medication versus recreational purposes. Distinct consumption patterns were observed, aligning with either recreational use or self-medication motives. The findings provide preliminary insights into potential associations between legal frameworks and consumption behaviors across countries with differing regulations. The results underscore the importance of developing standardized regulatory policies for various CBD products. Despite molecular evidence and results from animal models, further clinical trials are needed to establish the true efficacy of CBD. Future research should focus on examining dose-response relationships, different routes of administration, effects of isolated CBD, and assessing potential CBD-drug interactions. Additionally, RCTs are essential to differentiate the true therapeutic effectiveness from placebo effects, which are often reinforced by media or false advertisement.

Acknowledgements

We would like to express our heartfelt gratitude to all participants in the survey. We also extend our appreciation to all CBD manufacturers who assisted in disseminating the survey link. Special thanks to Gregor Wurth and the board of the DHV for their contributions to the distribution of the questionnaire.

Authors’ information

EK conducted this work in fulfillment of the requirements for the Master of Science (M.Sc.) degree. This study was conducted as a collaborative project between the IFT Institute for Therapy Research, Centre for Mental Health and Addiction Research, Munich, Germany; the Department of Psychiatry and Psychotherapy, University Hospital, Ludwig-Maximilians-University Munich, Munich, Germany; and the TUM School of Medicine and Health, Chair of Epidemiology, Technical University of Munich, Munich, Germany.

Author contributions

EK was responsible for conceptualization, conducting literature research, developing the questionnaire, managing online data collection, coordinating with retailers and manufacturers for study support, cleaning and analyzing of the data, and preparing the manuscript. CR contributed by reviewing the manuscript, providing edits throughout, and assisting with data analysis. SJK reviewed and edited the manuscript and supervised the project. LT supervised the project and was involved in questionnaire development. EH reviewed and edited the manuscript and supervised the project and was involved in the conceptualization of this project.

Funding

The work was conducted as part of a master’s thesis to obtain the academic degree M.Sc. and did not receive any funding, neither from CBD manufacturers nor from the German Hemp Association, which only assisted in disseminating the survey. The costs for the ethics application were covered by the IFT Institut für Therapieforschung, Center for Mental Health & Addiction Research.

Data availability

No datasets were generated or analysed during the current study.

Declarations

Ethics approval and consent to participate

Ethical approval was obtained from the ethics committee of the Technical University of Munich (ethics approval number: 2022-672-S-KK). By starting the questionnaire, participants consent to the use of their data for the described research purpose.

Consent for publication

Participants were informed that the data would be anonymized and that participation in the survey was voluntary. By starting the questionnaire, participants consent to the use of their data for the described publication.

Competing interests

The authors declare no competing interests.

Footnotes

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  1. Alayli AFG, Kotz D, Kastaun S. Recreational cannabidiol: awareness, prevalence of use, and associated factors in a representative sample of the German population. Subst Use Misuse. 2022;57(9):1417–24. [DOI] [PubMed] [Google Scholar]
  2. Beckmann L, Ist. CBD legal? 2024 [Available from: https://hanfgefluester.de/blogs/cbd-wissen/ist-cbd-legal?srsltid=AfmBOoqH4FDr2bN5PYCGCHv8_Unnz3xbNuX3FTf_yyCYRJit2jfE_zrV
  3. Bergamaschi MM, Queiroz RH, Zuardi AW, Crippa JA. Safety and side effects of cannabidiol, a cannabis sativa constituent. Curr Drug Saf. 2011;6(4):237–49. [DOI] [PubMed] [Google Scholar]
  4. Binkowska AA, Jakubowska N, Redeł A, Laskowska S, Szlufik S, Brzezicka A. Cannabidiol usage, efficacy, and side effects: analyzing the impact of health conditions, medications, and cannabis use in a cross-sectional online pilot study. Front Psychiatry. 2024;15:1356009. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Boyaji S, Merkow J, Elman RNM, Kaye AD, Yong RJ, Urman RD. The role of Cannabidiol (CBD) in chronic pain management: an assessment of current evidence. Curr Pain Headache Rep. 2020;24(2):4. [DOI] [PubMed] [Google Scholar]
  6. Bundesamt für Verbraucherschutz und Lebensmittelsicherheit. Sind Nahrungsergänzungsmittel mit Cannabidiol (CBD) (CBD) verkehrsfähig? [Available from: https://www.bvl.bund.de/SharedDocs/FAQ/DE/02_Unternehmer/01_Lebensmittel/03_FAQ_Hanf_THC_CBD/00_FAQ_Cannabidiol_CBD.html
  7. Britch SC, Babalonis S, Walsh SL. Cannabidiol: pharmacology and therapeutic targets. Psychopharmacology. 2021;238(1):9–28. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Brown JD, Winterstein AG. Potential adverse drug events and drug-drug interactions with medical and consumer Cannabidiol (CBD) use. J Clin Med. 2019. 10.3390/jcm8070989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Cerdá M, Mauro C, Hamilton A, Levy NS, Santaella-Tenorio J, Hasin D, et al. Association between recreational marijuana legalization in the united States and changes in marijuana use and cannabis use disorder from 2008 to 2016. JAMA Psychiatr. 2020;77(2):165–71. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Chagas MH, Crippa JA, Zuardi AW, Hallak JE, Machado-de-Sousa JP, Hirotsu C, et al. Effects of acute systemic administration of Cannabidiol on sleep-wake cycle in rats. J Psychopharmacol. 2013;27(3):312–6. [DOI] [PubMed] [Google Scholar]
  11. Cohen J. Statistical power analysis for the behavioral Sciences. Rev. ed. New York: Lawrence Erlbaum Associates; 1988. [Google Scholar]
  12. Corroon J, Phillips JA. A cross-sectional study of cannabidiol users. Cannabis Cannabinoid Res. 2018;3(1):152–61. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Costa B, Giagnoni G, Franke C, Trovato AE, Colleoni M. Vanilloid TRPV1 receptor mediates the antihyperalgesic effect of the nonpsychoactive cannabinoid, cannabidiol, in a rat model of acute inflammation. Br J Pharmacol. 2004;143(2):247–50. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Crippa JA, Derenusson GN, Ferrari TB, Wichert-Ana L, Duran FL, Martin-Santos R, et al. Neural basis of anxiolytic effects of cannabidiol (CBD) in generalized social anxiety disorder: a preliminary report. J Psychopharmacol. 2011;25(1):121–30. [DOI] [PubMed] [Google Scholar]
  15. Devinsky O, Cross JH, Laux L, Marsh E, Miller I, Nabbout R, et al. Trial of cannabidiol for drug-resistant seizures in the Dravet syndrome. N Engl J Med. 2017;376(21):2011–20. [DOI] [PubMed] [Google Scholar]
  16. Devinsky O, Marsh E, Friedman D, Thiele E, Laux L, Sullivan J, et al. Cannabidiol in patients with treatment-resistant epilepsy: an open-label interventional trial. Lancet Neurol. 2016;15(3):270–8. [DOI] [PubMed] [Google Scholar]
  17. Dingermann T. Grundlagen der pharmakologie von cannabinoiden. Schmerzmedizin. 2021;37(1):8–13. [Google Scholar]
  18. Efsa Panel on, Nutrition NF, Food A, Turck D, Bohn T, Castenmiller J, De Henauw S, et al. Statement on safety of Cannabidiol as a novel food: data gaps and uncertainties. EFSA J. 2022;20(6):e07322. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Engeli BE, Lachenmeier DW, Diel P, Guth S, Villar Fernandez MA, Roth A, et al. Cannabidiol in foods and food supplements: evaluation of health risks and health claims. Nutrients. 2025;17(3):489. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. European Parliament, Council of the European Union. Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use. 2001. [cited 2025 Oct 3]. Available from: https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX%3A32001L0083.
  21. Fakhfouri G, Rahimian R, Dyhrfjeld-Johnsen J, Zirak MR, Beaulieu JM. 5-HT(3) receptor antagonists in neurologic and neuropsychiatric disorders: the iceberg still Lies beneath the surface. Pharmacol Rev. 2019;71(3):383–412. [DOI] [PubMed] [Google Scholar]
  22. Fortin D, Di Beo V, Massin S, Bisiou Y, Carrieri P, Barré T. Reasons for using Cannabidiol: a cross-sectional study of French Cannabidiol users. J Cannabis Res. 2021;3(1):46. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Gali K, Winter SJ, Ahuja NJ, Frank E, Prochaska JJ. Changes in cannabis use, exposure, and health perceptions following legalization of adult recreational cannabis use in California: a prospective observational study. Subst Abuse Treat Prev Policy. 2021;16(1):16. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. García-Gutiérrez MS, Navarrete F, Gasparyan A, Austrich-Olivares A, Sala F, Manzanares J. Cannabidiol: a potential new alternative for the treatment of anxiety, depression, and psychotic disorders. Biomolecules. 2020. 10.3390/biom10111575. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Geppert J, Lietzow J, Hessel-Pras S, Kirsch F, Schäfer B, Sachse B. Usage and health perception of cannabidiol-containing products among the population in germany: a descriptive study conducted in 2020 and 2021. BMC Public Health. 2023;23(1):2318. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Goodman S, Wadsworth E, Schauer G, Hammond D. Use and perceptions of cannabidiol products in Canada and in the united States. Cannabis Cannabinoid Res. 2022;7(3):355–64. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Gournay LR, Ferretti ML, Zvorsky I, Fernandez DA, Leen-Feldner EW. Cannabidiol (CBD) products: use patterns and perceptions within a sample of anxious users. Subst Use Misuse. 2024;59(11):1604–12. [DOI] [PubMed] [Google Scholar]
  28. GW Pharma (International) B.V. Dossier zur Nutzenb. 2021. [cited 2025 Oct 3]. Available from: https://www.g-ba.de/downloads/92-975-4743/2021_05_14_Modul2_Epidyolex.pdf.
  29. Harris JK. Primer on binary logistic regression. Fam Med Community Health. 2021;9(Suppl 1):e001290. doi:10.1136/fmch-2021-001290. PMID: 34952854; PMCID: PMC8710907 [DOI] [PMC free article] [PubMed]
  30. Hurt L. Legal status of cannabis and CBD in the United Kingdom 2023 [Available from: https://cannactiva.com/en/cannabis-cbd-legal-uk/
  31. Iannotti FA, Vitale RM. The endocannabinoid system and ppars: focus on their signalling crosstalk, action and transcriptional regulation. Cells. 2021. 10.3390/cells10030586. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Ibeas Bih C, Chen T, Nunn AV, Bazelot M, Dallas M, Whalley BJ. Molecular targets of cannabidiol in neurological disorders. Neurotherapeutics. 2015;12(4):699–730. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Kim JH. Multicollinearity and misleading statistical results. Korean J Anesthesiol. 2019;72(6):558–69. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Kirsch S. CBD-Produkte nicht immer legal: Vorsicht bei Öl, Tee und Co. [Internet]. ZDFheute. 2023. [cited 2025 Oct 3]. Available from: https://www.zdfheute.de/ratgeber/cannabis-cbd-produkte-hanf-recht-100.html.
  35. Lachenmeier DW, Bock V, Deych A, Sproll C, Rajcic de Rezende T, Walch SG. Hanfhaltige Lebensmittel – ein Update. Deutsche Lebensmittel-Rundschau. 2019;115(8):351–72.
  36. Lachenmeier D. Einstufung von Cannabidiol (CBD) Aus Hanf – Ein Betäubungsmittel und Damit Ein Nicht-Lebensmittel? Dtsch Lebensmittel-Rundschau: Z für Lebensmittelkunde Und Lebensmittelrecht. 2020;116:347–8. [Google Scholar]
  37. Leweke FM, Piomelli D, Pahlisch F, Muhl D, Gerth CW, Hoyer C, et al. Cannabidiol enhances anandamide signaling and alleviates psychotic symptoms of schizophrenia. Transl Psychiatry. 2012;2(3):e94. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Linares IMP, Guimaraes FS, Eckeli A, Crippa ACS, Zuardi AW, Souza JDS, et al. No acute effects of Cannabidiol on the Sleep-Wake cycle of healthy subjects: A Randomized, Double-Blind, Placebo-Controlled, crossover study. Front Pharmacol. 2018;9:315. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Soliman N, Haroutounian S, Hohmann AG, Krane E, Liao J, Macleod M, et al. Systematic review and meta-analysis of cannabinoids, cannabis-based medicines, and endocannabinoid system modulators tested for antinociceptive effects in animal models of injury-related or pathological persistent pain. Pain. 2021;162(Suppl 1):S26–44. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Manthey J, Hayer T, Jacobsen B, Kalke J, Klinger S, Rehm J, Rosenkranz M, Verthein U, Wirth M, Armstrong M, Myran D, Pacula R, Queirolo R, Zobel F. Technischer Bericht: Auswirkungen der Legalisierung von Cannabis. Berlin: Federal Ministry of Health. 2023. Available from: https://www.bundesgesundheitsministerium.de/fileadmin/Dateien/5_Publikationen/Drogen_und_Sucht/Abschlussbericht/230623_Technical_Report_de_bf.pdf.
  41. McGregor IS, Cairns EA, Abelev S, Cohen R, Henderson M, Couch D, et al. Access to cannabidiol without a prescription: a cross-country comparison and analysis. Int J Drug Policy. 2020;85:102935. [DOI] [PubMed] [Google Scholar]
  42. Mead A. The legal status of cannabis (marijuana) and Cannabidiol (CBD) under U.S. law. Epilepsy Behav. 2017;70(Pt B):288–91. [DOI] [PubMed] [Google Scholar]
  43. Melchert D, Schaare F, Winterhalter P, Beuerle T. CBD products: labeling accuracy of an obscure niche market. Food Control. 2024;160:110375. [Google Scholar]
  44. Mennis J, McKeon TP, Stahler GJ. Recreational cannabis legalization alters associations among cannabis use, perception of risk, and cannabis use disorder treatment for adolescents and young adults. Addict Behav. 2023;138:107552. [DOI] [PubMed] [Google Scholar]
  45. Moltke J, Hindocha C. Reasons for cannabidiol use: a cross-sectional study of CBD users, focusing on self-perceived stress, anxiety, and sleep problems. J Cannabis Res. 2021;3(1):5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. Moore A, Straube S, Fisher E, Eccleston C. Cannabidiol (CBD) products for pain: Ineffective, Expensive, and with potential harms. J Pain. 2024;25(4):833–42. [DOI] [PubMed] [Google Scholar]
  47. Notcutt W, Price M, Miller R, Newport S, Phillips C, Simmons S, et al. Initial experiences with medicinal extracts of cannabis for chronic pain: results from 34 ‘N of 1’ studies. Anaesthesia. 2004;59(5):440–52. [DOI] [PubMed] [Google Scholar]
  48. Pisanti S, Malfitano AM, Ciaglia E, Lamberti A, Ranieri R, Cuomo G, et al. Cannabidiol: state of the art and new challenges for therapeutic applications. Pharmacol Ther. 2017;175:133–50. [DOI] [PubMed] [Google Scholar]
  49. Reekie TA, Scott MP, Kassiou M. The evolving science of phytocannabinoids. Nat Rev Chem. 2017;2(1):0101. [Google Scholar]
  50. Russo EB. History of cannabis and its preparations in saga, science, and sobriquet. Chem Biodivers. 2007;4(8):1614–48. [DOI] [PubMed] [Google Scholar]
  51. Silvestro S, Schepici G, Bramanti P, Mazzon E. Molecular targets of cannabidiol in experimental models of neurological disease. Molecules. 2020. 10.3390/molecules25215186. [DOI] [PMC free article] [PubMed] [Google Scholar]
  52. Soleymanpour M, Saderholm S, Kavuluru R. Therapeutic claims in Cannabidiol (CBD) marketing messages on Twitter. Proc (IEEE Int Conf Bioinf Biomed). 2021;2021:3083–8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  53. Statista CBD. Products - Germany 2024 [Available from: https://www.statista.com/outlook/hmo/cannabis/cbd-products/germany
  54. Suraev AS, Marshall NS, Vandrey R, McCartney D, Benson MJ, McGregor IS, et al. Cannabinoid therapies in the management of sleep disorders: a systematic review of preclinical and clinical studies. Sleep Med Rev. 2020;53:101339. [DOI] [PubMed] [Google Scholar]
  55. Thiele EA, Bebin EM, Bhathal H, Jansen FE, Kotulska K, Lawson JA, et al. Add-on cannabidiol treatment for drug-resistant seizures in tuberous sclerosis complex: a placebo-controlled randomized clinical trial. JAMA Neurol. 2021;78(3):285–92. [DOI] [PMC free article] [PubMed] [Google Scholar]
  56. Thiele EA, Marsh ED, French JA, Mazurkiewicz-Beldzinska M, Benbadis SR, Joshi C, et al. Cannabidiol in patients with seizures associated with Lennox-Gastaut syndrome (GWPCARE4): a randomised, double-blind, placebo-controlled phase 3 trial. Lancet. 2018;391(10125):1085–96. [DOI] [PubMed] [Google Scholar]
  57. U.S. Centers for Disease Control and Prevention. Cigarette Smoking: U.S. Centers for Disease Control and Prevention; 2024 [Available from: https://www.cdc.gov/tobacco/about/index.html
  58. VanDolah HJ, Bauer BA, Mauck KF. Clinicians’ guide to Cannabidiol and hemp oils. Mayo Clin Proc. 2019;94(9):1840–51. [DOI] [PubMed] [Google Scholar]
  59. Verbraucherzentrale. CBD-Öl legal auf dem Markt? [updated 13.08.2025. Available from: https://www.verbraucherzentrale.de/wissen/lebensmittel/nahrungsergaenzungsmittel/cbdoel-legal-auf-dem-markt-37660
  60. Verbraucherzentrale. Vorsicht bei Lebensmitteln mit dem Hanf-Inhaltsstoff Cannabidiol (CBD) [updated 18.10.2023. Available from: https://www.verbraucherzentrale.de/wissen/lebensmittel/nahrungsergaenzungsmittel/vorsicht-bei-lebensmitteln-mit-dem-hanfinhaltsstoff-cannabidiol-cbd-43455
  61. Verbraucherzentrale Sachsen-Anhalt. Süßwaren mit Cannabidiol (CBD) – riskante Verwechslungsgefahr für Kinder. 2024. [cited 2025 Oct 3]. Available from: https://www.verbraucherzentrale-sachsen-anhalt.de/pressemeldungen/lebensmittel/suesswaren-mit-cannabidiol-cbd-riskante-verwechslungsgefahr-fuer-kinder-100033.
  62. Verbraucherzentrale Baden-Württemberg. CBD in Nahrungsergänzungsmitteln ist für Schmerzbehandlungen ungeeignet [updated 01.07.2019. Available from: https://www.verbraucherzentrale-bawue.de/wissen/lebensmittel/nahrungsergaenzungsmittel/cbd-in-nahrungsergaenzungsmitteln-ist-fuer-schmerzbehandlungen-ungeeignet-37672
  63. Wallace JE, Kogan LR, Carr ECJ, Hellyer PW. Motivations and expectations for using cannabis products to treat pain in humans and dogs: a mixed methods study. J Cannabis Res. 2020;2(1):36. [DOI] [PMC free article] [PubMed] [Google Scholar]
  64. Walukevich-Dienst K, Morris PE, Tucker RP, Copeland AL, Buckner JD. Development and initial psychometric properties of the cannabidiol outcome expectancies questionnaire (CBD-OEQ). Psychol Assess. 2022;34(7):643–59. [DOI] [PMC free article] [PubMed] [Google Scholar]
  65. Wissenschaftliche Dienste des Deutschen Bundestages. Verkehrsfähigkeit von Cannabidiol (CBD) als Arzneimittel: Überblick über die wesentlichen rechtlichen Vorgaben. Berlin: German Bundestag. 2020. [cited 2025 Oct 3]. Available from: https://www.bundestag.de/resource/blob/681702/7e584f6acd93c0a5dc7330c10e569e1c/WD-9-046-19-pdf-data.pdf.

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

No datasets were generated or analysed during the current study.


Articles from Journal of Cannabis Research are provided here courtesy of BMC

RESOURCES