NewsNeuropsychopharmacologyOct 31, 2026 · 14 min read

Do Women Feel THC More? In a 44-Person Trial, Occasional-Use Men Felt It Most

A UCLA placebo-controlled trial published October 29, 2026 gave 44 adults smoked cannabis at 0%, 4% and 10% THC. Women did not report stronger effects than men; occasional-use men reported the most unpleasant ones. Frequency findings were exploratory.

Do Women Feel THC More? In a 44-Person Trial, Occasional-Use Men Felt It Most

A placebo-controlled trial from UCLA, published online on October 29, 2026 in Neuropsychopharmacology, tested whether women feel smoked THC more than men do. In 44 adults, they did not. The 10 men who used cannabis only occasionally reported the most unpleasant effects, even though their blood THC was similar to that of occasional-use women. It is one small trial of low-strength flower, and it cannot tell you how much anyone should use.

What the UCLA team did

The paper is a randomized controlled trial titled Sex- and frequency-dependent acute pharmacokinetic and pharmacodynamic effects of smoked cannabis, published online on October 29, 2026 in Neuropsychopharmacology by first author Stephanie Lake, senior author Ziva D. Cooper and colleagues at the UCLA Center for Cannabis and Cannabinoids (doi 10.1038/s41386-026-02571-3). It is open access, and we read the full text, not only the abstract. The design has a long name, and each word matters. Randomized means the order of the three cigarettes was assigned by chance. Double-blind means neither the participants nor the staff running the sessions knew which strength was in use. Placebo-controlled means one of the three cigarettes contained essentially no THC. Crossover means every participant smoked all three, on separate days, so each person serves as their own comparison. The authors describe it as the first study to experimentally investigate both sex and cannabis use frequency together.

The 44 healthy adults were split evenly by sex and, within each sex, by how often they used in the past month. On average, the frequent groups used about 6 days a week (6.1 for men, 5.9 for women) and the occasional groups about 2 (2.0 for men, 2.3 for women). The women's sessions were timed to the mid-to-late follicular phase of the menstrual cycle, when estradiol is high and progesterone is low: the point where the authors expected a sex difference to be largest. People seeking treatment for their cannabis use, people with current pain, and people with a BMI under 18.5 or over 34 were excluded.

44
adults: 22 women and 22 men
3
strengths smoked: 0%, 4% and 10% THC
6 h
per session, at least 48 hours apart
161
enrolled in the larger registered trial
ElementWhat the trial did
Participants44 healthy adults aged 21 to 55: 22 women, 22 men
GroupsPer sex: 12 frequent users (more than 4 days a week) and 10 occasional users (4 days a week or fewer)
Strengths0%, 4% and 10% THC (about 0, 20 and 60 mg of THC available in the cigarette), one per session, in random order
CannabisSupplied by NIDA; about 560 mg of an 800 mg cigarette smoked with timed, paced puffs
SessionsThree 6-hour outpatient sessions (9:00 to 15:00), at least 48 hours apart, each after 21 hours without cannabis
Measures44-item mood and physical-effect scales (0 to 100), drug-effect ratings ("Strength", "Good effect", "Bad effect", "Like", "Take again"), heart rate, blood pressure, temperature, and plasma THC, 11-OH-THC and THC-COOH
Choice taskAt 165 minutes, the option to buy 1 to 3 more puffs of the same strength at $1 a puff from study earnings
Women's timingMid-to-late follicular phase, confirmed by blood hormones; no hormonal birth control
RegistrationNCT04385082, registered May 2020
Study design, from the full text of Lake et al., Neuropsychopharmacology, published online October 29, 2026. The mg figures describe the THC available in each study cigarette; they are not guidance.

The trial was registered on ClinicalTrials.gov in May 2020 as NCT04385082, a study called CanSex. The 44 people in this paper are its pharmacokinetic sub-component, one slice of a larger trial. The registry lists 161 participants enrolled, a start date of July 8, 2021 and completion on July 30, 2026. It also names a pain outcome, measured with a cold pressor test (holding a hand in ice water), that is not part of this paper. No results are posted on the registry yet.

What it found, with every result labelled

Before the numbers, one distinction decides how much weight each can carry. Some results came straight out of the trial's main statistical models; we call those confirmatory. Others came from follow-up tests the authors ran on statistical trends, and those are exploratory. The trial had about 80% power to detect a moderate overall effect of cannabis, but only large differences between subgroups, and each subgroup held just 10 or 12 people. So every row below carries its label, and so does every sentence in this article that mentions an exploratory result.

FindingStatusNumbers
Active cannabis (4% and 10%) raised subjective effects and plasma THC and metabolitesConfirmatoryp < 0.05
Dysphoric arousal (unpleasant mood ratings) rose only in occasional-use menConfirmatory (p = 0.004)+20.4 points at 4% (13.0 to 27.8)
"Bad effect" ratings followed the same patternConfirmatory (p = 0.001)Rose only in occasional-use men
"High" was higher in occasional-use men than in frequent-use men, averaged across strengthsConfirmatory21.6 points (5.5 to 37.7)
At 4%, occasional-use men rated "High" above occasional-use women and above frequent-use menExploratory32.3 points (9.8 to 54.9) and 29.2 points (7.5 to 50.8)
Sedation and impairment rose only in the occasional groupConfirmatory (p = 0.016)+15.3 points at 4%
Within the occasional group, the sedation rise held only in menExploratory+22.3 points at 4%
Heart rate, adjusted for blood THC, rose only in the occasional groupConfirmatory (p = 0.039)+20.4 bpm at 4% (7.0 to 33.8)
Within the occasional group, the heart-rate rise held only in menExploratory+32.5 bpm at 4% (15.6 to 49.4)
Peak plasma THC at 4% was higher in frequent users than occasional usersConfirmatory (p = 0.014)+42.3 ng/mL (8.9 to 75.7)
Among frequent users, men had higher plasma THC at 4% than womenExploratory+57.1 ng/mL (9.8 to 104.3)
11-OH-THC was higher in men than women, and in frequent than occasional usersConfirmatory across strengths; concentration at 4% exploratoryNot summarized as one number
"Like" and "Take again" rose only in frequent users, regardless of sexExploratory (trends p = 0.095 and 0.060)Partly driven by occasional users' higher placebo "Like" (18.4 points)
Frequent users were more likely to buy extra puffs of active cannabisExploratory (trend p = 0.057)20.8%, 37.5% and 54.2% of frequent users at 0%, 4% and 10%
Ratings use 0 to 100 scales (a 100 mm line), so "points" are millimeters. Differences are versus placebo unless the row names another group. Parentheses show 95% confidence intervals. Source: Lake et al., Neuropsychopharmacology, October 29, 2026.

The clearest signal, then, is about the 10 occasional-use men. On the confirmatory tests, they were the only group whose dysphoric arousal and "Bad effect" ratings rose above placebo. That was not because more THC reached their blood: the authors note that these men responded more strongly despite peak plasma THC and 11-OH-THC similar to occasional-use women. Why, the trial cannot say. The authors raise one alternative they could not rule out. The occasional-use women were slightly older and had been using cannabis for longer (14.6 years since first use, against 9.8 for occasional-use men), so they may have carried more tolerance for reasons unrelated to sex. With 10 people in each of those groups, chance cannot be ruled out either.

One more pattern runs through the results. On most measures, the 10% cigarette did not produce clearly bigger effects than the 4% one, a flat or even inverted strength-response. The 10% cigarette also took more puffs to finish, 12.4 against 7.8 on average, and the authors suspect people took smaller puffs of the stronger cigarette, a kind of self-titration. Puff size was not measured, so that is their interpretation, not a result.

Grid of the four groups: frequent-use women (12) and men (12), occasional-use women (10) and men (10). The occasional-use men cell is marked for the most unpleasant effects (confirmatory); the frequent-use row for liking and extra puffs (exploratory).
Who reported what. Group sizes and labels from Lake et al., Neuropsychopharmacology, October 29, 2026. Exploratory results are leads, not findings.

How often you use shaped the results

If sex did not line up the way the usual story predicts, use frequency did on several measures. Frequent users had higher peak plasma THC at 4%, by 42.3 ng/mL (our explainer covers how THC moves through and clears from the blood). They also had higher levels of 11-OH-THC, the active metabolite the body makes from THC. Yet with more THC in their blood, they reported less of some effects: sedation and impairment rose above placebo only in the occasional group, the heavy, slowed-down feeling people often call couch-lock. In the model adjusted for blood THC, heart rate rose above placebo only in the occasional group too. Our report on an earlier trial that tracked heart rate after THC and CBD explains why a single session's heart-rate change is a measurement, not a verdict on safety.

More THC in the blood with fewer effects is the pattern researchers associate with tolerance, and it matches older work. In a 2009 study comparing 12 occasional and 12 heavy cannabis users, smoked THC impaired occasional users on tracking, divided attention and stop-signal tasks, but heavy users only on the stop-signal task; its authors concluded that cannabis use history strongly determines the behavioral response to a single dose of THC. Our guide to how tolerance builds and what taking a break can reset walks through that mechanism. Keep in mind that the new trial measured single sessions. It shows how frequent and occasional users differed on the day, not how tolerance develops over time.

The finding most likely to be summarized as "frequent users want more" is also the most tentative. In an exploratory analysis of statistical trends (p = 0.095 and 0.060), "Like" and "Take again" ratings rose above placebo only in the frequent group, and sex did not change that. Part of the gap came from the other side: occasional users rated the placebo cigarette higher on "Like" (18.4 points). In the self-administration task, also exploratory (trend p = 0.057), frequent users were more likely to buy extra puffs of active cannabis (54.2% of them at 10%, against 20.8% after placebo), while occasional users were most likely to buy after placebo. The authors read this, cautiously, as "suggesting misuse-liability related to frequency, independent of sex." Ratings like these are laboratory markers researchers use for misuse liability, the pull a drug has to be used again. They are not a diagnosis, and they say nothing about any individual reader's risk.

A gloved hand placing a capped blood collection tube into a plastic rack on a clinical lab bench, other tubes in soft focus behind it.
The trial drew blood across each 6-hour session to measure THC and its metabolites, which is how it could tell that occasional-use men's stronger reactions were not explained by higher blood levels.

Why it cuts against the usual story

Search for whether women get higher than men and most of what you find says yes, often pointing to hormones. Much of that idea comes from animals. The rat studies the authors summarize in their introduction found that female rats recognize THC at lower doses, self-administer cannabinoid drugs faster and in larger amounts, show sensitivity that depends on estradiol, and produce more 11-OH-THC. A 2018 review of sex differences in cannabis effects, published in the same journal, set that preclinical picture alongside the human data. Rat findings are a reason to test a question in people. They are not an answer about people.

“These findings contrast with previous evidence of greater cannabis sensitivity among females.”
Lake et al., Neuropsychopharmacology, October 29, 2026

The human evidence before this trial was already mixed, and the way THC was taken differed from study to study. Here is what the earlier human studies found, with the design details that limit each one.

Year, journalWho and howWhat it found by sexMain limit
2014, Drug and Alcohol DependencePooled 4 studies; 35 men, 35 women, daily smokers; 3.27% to 5.50% THC smokedWomen rated "Good" and "Take again" higher; no difference in "High"; heart rate rose equallySecondary pooled analysis; daily users only
2017, Pharmacology Biochemistry and BehaviorRetrospective; 18 men, 12 women; oral THC 5 to 30 mgWomen more sensitive at 5 mg, men more sensitive at 15 mgSmall and retrospective
2020, Psychopharmacology91 adults aged 19 to 25, using 1 to 4 days a week; 12.5% THC smoked as they choseWomen smoked less and had lower blood THC, with the same effects as menUnbalanced (17 women in the active group)
2021, Addiction BiologyPooled 4 trials; 27 men, 23 women, infrequent users; oral and vaporized THC 5 to 25 mgWomen had a higher peak drug effect and higher 11-OH-THC, and felt more anxious and restlessDifferent routes; pooled
2022, Addiction BiologyPooled 2 trials; 21 men, 19 women; vaporized THC 13.75 mg with or without CBD"An absence of systematic sex differences"One moderate dose, vaporized
2023, Addiction BiologyPooled 2 trials; 55 men, 13 women, at least weekly users; about 25 mg THC smokedWomen rated strength, liking, take-again and good effect higher; self-administration not differentOnly 13 women; same lab as the new trial
2024, PsychopharmacologyCrossover trial; 56 adults; oral dronabinol 10 mgWomen rated their high higher (p = 0.05); other effects similarOne oral pharmaceutical dose
Earlier human studies of sex differences in THC effects, from their PubMed abstracts, read October 31, 2026. Doses describe what each study gave, not guidance.

Two of the studies that pointed toward women come from this same research group: a 2014 pooled analysis of daily cannabis smokers and a 2023 pooled analysis of two smoked-cannabis trials, which included only 13 women. Among infrequent users, a 2021 pooled analysis of oral and vaporized THC also leaned toward women. On the other side, a 2020 study of 91 young adults smoking cannabis as they chose found women reached the same effects at lower blood THC, a 2022 pooled analysis of vaporized THC reported no systematic sex differences, and a small retrospective study of oral THC found the direction flipped with dose. A 2024 crossover trial of oral dronabinol, a pharmaceutical form of THC, found women rated their high higher, right at the edge of statistical significance (p = 0.05).

Put together, the human record was never a clean "women feel it more." What the new trial adds is a design built for the question: balanced by sex and by frequency, with every person getting every strength and placebo, and with women tested at a fixed point in their cycle. It does not overturn the earlier studies. It disagrees with some of them, in a different sample, and that disagreement is now on the record for the next trial to resolve.

What this study does not tell you

  • It is not dose guidance. The 20 mg and 60 mg figures describe the THC available in the study cigarettes, not an amount anyone should use.
  • It does not show that women can handle more or that men should use less. It describes 44 adults at one site, with 10 or 12 people in each subgroup.
  • It tested smoked flower only. Edibles, vapes, concentrates and CBD products were not studied.
  • The strengths were 4% and 10% THC, below the 20% or more the authors say is typical of commercial cannabis.
  • Women were tested in one phase of the menstrual cycle, and women using hormonal birth control were excluded, so other phases and contraceptive users remain open questions.
  • Each strength was a single session. Long-term tolerance, dependence and everyday use were not measured.
  • Several of the sex and frequency results are exploratory, with no correction for multiple comparisons.
  • Puff size was not measured, and the self-administration task was scored only as yes or no.
  • Adverse events and the parent trial's pain results are to be reported elsewhere, not in this paper.

On potency: Washington State retail sales data from 2014 to 2016 put the average THC content of flower at 20.6%, about twice the trial's strongest cigarette. Effects at retail strengths could look different. Our explainer on whether the THC percentage on a label predicts how strong flower feels covers why that number is only part of the picture. And because this trial was about THC, it says nothing about CBD, which is a different molecule with a different profile; if dependence is your question there, see whether CBD is addictive.

Bar chart of THC strength: the trial's cigarettes at 0%, 4% and 10%, beside the 20.6% average for flower sold in Washington State from 2014 to 2016.
The trial's strengths against retail flower. Study figures from Lake et al., 2026; retail average from Washington State sales data, 2014 to 2016 (Smart et al., Addiction, 2017).

Who ran it and who paid

We print the disclosures because you should be able to see them alongside the results. Listing them does not imply they changed the results, and the funding for this trial came from public and charitable sources.

What to watch next

The parent trial finished on July 30, 2026 with 161 people enrolled, so more papers should follow. The registry names pain response (measured with the cold pressor test) as a primary outcome, and the authors say adverse events will be reported elsewhere. They are direct about why their own result needs testing again, citing "our modest sample size and reliance on exploratory follow-up, the potential for unmeasured confounding, and that our findings did not extend to all observed outcomes." They call for larger samples and finer categories of use frequency than a single line at 4 days a week. Until then, this is one well-designed, small trial that disagrees with part of the earlier evidence.

Frequently asked questions

Not in this trial. Among 44 adults smoking identical cigarettes, women did not report a stronger high than men. Occasional-use men rated their high above frequent-use men, and in an exploratory comparison at 4% also above occasional-use women. Earlier pooled studies found women rated some rewarding effects higher, so one trial does not settle it.

The trial could not test that. Every woman was tested in the mid-to-late follicular phase, when the authors expected the largest difference, and the expected female sensitivity did not appear. Other phases, and women using hormonal birth control, were not studied.

The results fit that idea: frequent users had higher blood THC at 4%, yet sedation rose above placebo only in occasional users. These were single sessions, so the trial shows a difference between groups on the day, not tolerance developing over time.

The trial cannot explain it; their blood THC was similar to occasional-use women's. The authors note those women were slightly older and had used cannabis for longer, which could mean more tolerance unrelated to sex. With 10 people per group, chance is also possible.

No. Everyone smoked flower. Edibles, vapes, concentrates and CBD were not studied, and earlier studies of oral and vaporized THC reported different patterns by sex.

No. The cigarettes were 4% and 10% THC; the authors note commercial cannabis is typically 20% THC or more. Effects at retail strengths could differ.

NIH institutes (NIDA, NCCIH and NCATS), the Semel Charitable Foundation and trainee grants. Outside this work, the senior author reports receiving study drug from Canopy Growth Corp and True Terpenes and study-related materials from Storz & Bickel, and she is an associate editor of the journal that published it.

If this trial made you curious about your own pattern of use, the most useful next read is our guide to cannabis tolerance and tolerance breaks, which covers what frequent use does to how THC feels and what changes when you pause. We will update this page when the parent trial's other results are published.

#Research#THC#Clinical trials#Tolerance#Sex differences
P
Planntz Editorial Team
Editorial team

Writing about hemp, wellness and the small rituals that keep us balanced.

Latest news

From the newsroom

HHS Proposes Changes to Federal Drug Testing: What Changes, and What Stays the Same for THC and CBDU.S. Department of Health and Human Services, SAMHSA (Federal Register 2026-22122)01

HHS Proposes Changes to Federal Drug Testing: What Changes, and What Stays the Same for THC and CBD

HHS proposed revisions to the federal workplace drug-testing guidelines on October 29, 2026. Most changes are lab mechanics. Marijuana stays on every test, cutoffs do not move, and secondhand smoke is still not an accepted explanation. Comments close December 28.

Oct 30, 2026·10 min read
A Pilot Trial Gave Knee-Replacement Patients Prescription CBD. It Missed Its Main Goal.J Pain02

A Pilot Trial Gave Knee-Replacement Patients Prescription CBD. It Missed Its Main Goal.

On October 22, 2026, The Journal of Pain published a triple-blind pilot trial of prescription CBD in 36 knee-replacement patients. Neither dose significantly changed 72-hour opioid use. A post hoc signal at 400 mg needs a larger trial; 800 mg brought more side effects.

Oct 24, 2026·18 min read
Cochrane Reviewed Medical Cannabis for Insomnia: What It Found, and What It Could Not TestCochrane Database of Systematic Reviews (CD016216, 2026)03

Cochrane Reviewed Medical Cannabis for Insomnia: What It Found, and What It Could Not Test

On October 13, 2026, Cochrane pooled 9 randomized trials in 537 adults with insomnia. Medical cannabis may have little to no clinically meaningful effect on sleep, on very low-certainty evidence, with more adverse events (low certainty).

Oct 13, 2026·15 min read
DEA Proposes a New 7-OH Threshold and Withdraws the July One: What Changes, and WhenU.S. Drug Enforcement Administration (Federal Register 2026-20943)04

DEA Proposes a New 7-OH Threshold and Withdraws the July One: What Changes, and When

On October 9, 2026, DEA filed a notice of intent proposing a new 7-OH threshold: more than 1 mg per gram or per mL, or a mitragynine ratio under 100. DEA says it is withdrawing the July 6 version. No order can issue before November 13, 2026.

Oct 10, 2026·16 min read
FDA Drops Premarket Review for Federal Drug-Test Devices: What Changed, and What Did NotU.S. Food and Drug Administration (Federal Register 2026-20448)05

FDA Drops Premarket Review for Federal Drug-Test Devices: What Changed, and What Did Not

On October 6, 2026, FDA let drug-test systems in 14 categories, including cannabinoid tests, skip 510(k) review for federal programs. Saliva testing for DOT jobs is still not here: HHS's latest list shows no certified oral-fluid lab.

Oct 6, 2026·14 min read
WADA's 2027 Cannabinoid Rule: CBD Is Still Allowed, and the Blanket Clause Is GoneWorld Anti-Doping Agency06

WADA's 2027 Cannabinoid Rule: CBD Is Still Allowed, and the Blanket Clause Is Gone

WADA published its 2027 Prohibited List on September 21, 2026. CBD is still not prohibited and THC still is, in-competition. The sentence that banned all natural and synthetic cannabinoids is gone, and WADA has not said what that means for CBG, CBN or THCV.

Sep 23, 2026·18 min read
An Appeals Court Left Medical Marijuana in Schedule III. It Did Not Decide the CaseU.S. Court of Appeals, D.C. Circuit07

An Appeals Court Left Medical Marijuana in Schedule III. It Did Not Decide the Case

On September 9, 2026 the D.C. Circuit denied a stay of the April order placing state-licensed medical marijuana in Schedule III. The challenges are still pending, broader rescheduling is still a proposal, and the rule says it does not affect hemp.

Sep 14, 2026·17 min read
A Randomized Trial Gave 18 Adults 12.5 mg of THC, With and Without CBD. Both Oils Raised Heart Rate.Br J Clin Pharmacol08

A Randomized Trial Gave 18 Adults 12.5 mg of THC, With and Without CBD. Both Oils Raised Heart Rate.

A randomized, double-blind crossover trial published on August 27, 2026 gave 18 healthy adults 12.5 mg of THC, with and without 12.5 mg of CBD, then made them breathe against a resistance. Both oils raised heart rate. Here is what the record supports and what it does not.

Sep 12, 2026·20 min read
A Trial Tested CBD Ads. The Control Group Is the StoryClinicalTrials.gov09

A Trial Tested CBD Ads. The Control Group Is the Story

On August 28, 2026 results were posted for a randomized trial that put 460 shoppers through a simulated mini mart. In the room with no CBD advertising at all, shoppers endorsed 5.6 of 12 listed benefits and 163 of 230 bought a CBD-branded product anyway.

Sep 7, 2026·23 min read
The FDA GRAS Proposal: How a New Ingredient Reaches a Shelf, and Why It Names Delta-8 THCFederal Register010

The FDA GRAS Proposal: How a New Ingredient Reaches a Shelf, and Why It Names Delta-8 THC

On August 11, 2026 FDA proposed making GRAS notification mandatory, and it names Delta-8 THC foods among its five examples. It is a proposal: comments close December 9, 2026, two days before the federal hemp-definition change takes effect.

Sep 6, 2026·25 min read
DEA Scheduled Three Kratom Analogs on August 26. It Did Not Schedule 7-OHFederal Register011

DEA Scheduled Three Kratom Analogs on August 26. It Did Not Schedule 7-OH

On August 26, 2026 DEA placed three kratom-derived analogs in Schedule I by temporary order: mitragynine pseudoindoxyl, MGM-15 and MGM-16. It did not schedule 7-hydroxymitragynine and it did not name kratom leaf. The HHS comment window closes September 10, 2026.

Sep 4, 2026·25 min read
Congress Moved the Hemp Deadline to December 11, and Left One Piece on November 12The White House012

Congress Moved the Hemp Deadline to December 11, and Left One Piece on November 12

On September 2, 2026 a single-sentence section inside H.R. 6500 split the 2026 hemp deadline in two. Most of the new definition now arrives on December 11, 2026. One exclusion still arrives on November 12, and it is the one whose official list does not exist.

Sep 3, 2026·23 min read