Tuning daytime and evening light did not improve older adults' sleep
In a 12-person crossover trial, blue-enriched daytime light with reduced evening blue did not cut time spent awake at night, though it nudged a brainwave marker of sleep.
For how we live.
In a 12-person crossover trial, blue-enriched daytime light with reduced evening blue did not cut time spent awake at night, though it nudged a brainwave marker of sleep.
In 216 patients with chronic patellofemoral pain across 10 Korean hospitals, an 8-week digital therapeutic beat education and exercise instruction on pain — by 12.5 mm on a 100 mm scale.
A small double-blind trial found a single 5.5 mg/kg dose lifted sprint power for hours, alongside higher noradrenaline and lower perceived effort — but it was 12 people, mostly men.
In the 172-patient PARADIGM trial, azacitidine plus venetoclax more than doubled median event-free survival versus induction chemotherapy — but it was a phase 2 study not powered for overall survival.
In the Ket-BD trial, four IV ketamine infusions over two weeks lowered depression scores more than an active placebo, with no manic switches observed in 63 analysed patients.
In 69 people across normal weight, overweight and type 2 diabetes, a stevia drink behaved like water — no shift in glucose, insulin, gut hormones, appetite or how much they ate next.
In a 40-person crossover trial, 10 mg and 20 mg of edible THC degraded lane-keeping while whole-blood THC peaked at 1.6 and 3.4 ng/mL — near or under the thresholds police enforce.
STAREE randomised 9,971 Australians aged 70 and over to atorvastatin or placebo. Cardiovascular events fell by 30%. Death, dementia and persistent disability, taken together, did not move.
Dense tissue raises breast-cancer risk and hides cancers on a mammogram. US facilities must now tell patients — but the evidence on what to do next is a real trade-off: more cancers found, more false alarms.
A 293-woman Dutch trial found more women reported improvement at 12 months with perioperative oestriol cream than placebo. Anatomical success, surgical success and reintervention were unchanged.
SleepCARE randomised 219 Australian women receiving chemotherapy for breast cancer to CBT-I, bright light therapy, both, or sleep hygiene. Only CBT-I moved insomnia — and nothing moved fatigue.
A meta-analysis of 116 randomised trials found weight, waist and body fat falling steadily up to 300 minutes a week. In one 24-week trial, 48% of participants compensated by about 308 kcal a day.
In one study of 62,685 women, iron deficiency prevalence ranged from 3% to 15% depending on the ferritin threshold. On treatment, a recent trial found alternate-day iron caused fewer side effects than daily dosing.
Observational studies had linked proton pump inhibitors to fractures, dementia, kidney disease and more. A randomised trial collected all of those outcomes and found only enteric infections.
The TAME trial randomised 276 adults with diagnosed anxiety disorders to mindfulness-based stress reduction or escitalopram. The difference on the primary measure was 0.07 points, inside the noninferiority margin.
FIMPACT enrolled 210 people, assigned them to real surgery, fake surgery or exercise, and followed them to 2023. The gap between operated and pretend-operated groups was 1.5 points on a 100-point scale.
OPAL randomised 347 people in Australian primary care and emergency departments. At six weeks the opioid group's mean pain score was slightly worse than the placebo group's.
Most women have a recurrence within a year of standard treatment. A 2025 trial stopped early once treating a woman alone proved inferior to treating her and her male partner together.
Weekly fluconazole kept most women free of thrush during treatment, yet by 12 months, six months after stopping, the advantage had narrowed sharply. A newer drug shows more durable suppression.
In the 240-woman ALTAR trial, methenamine hippurate was non-inferior to standard low-dose antibiotic prophylaxis over a year. Most other non-antibiotic prevention strategies still rest on weak evidence.
The PERTH trial is a 60-person pilot, and its outcome was urinary chemistry rather than health. Within those limits it answered a question people keep asking.
An 876-participant double-blind trial across 24 Chinese fertility centres nearly doubled serum 25-OHD in women with PCOS. Live births were 52.0% against 50.2% on placebo.
SCREESCO randomised Swedish 60-year-olds to colonoscopy, stool testing, or nothing. After a median 4.8 years, overall cancer incidence barely moved; the stage distribution did.
A four-arm randomised trial in 112 young women tested whether high-intensity circuit training and sleep-health counselling add up. On objective measures they did — by minutes.
A 250-person randomised trial paired a wearable tracker with just-in-time energy-management messages. Post-exertional malaise fell in both arms, and the difference between them was trivial.
A 1,151-person Hong Kong trial used trained lay counsellors, not clinicians, and no internet. The effect sizes are small, and the authors are explicit that they do not know whether it travels.
The LIDA trial tested whether romosozumab's bone-building window closes early enough to shorten treatment. It met non-inferiority on hip bone density — at a single centre, with 50 participants, over one year.
The PROP OA trial found a 3.39-point gain on a 100-point score at six months. The effect on pain was larger than the effect overall, and both diminished by twelve months.
In a 618-person randomized trial, 27.8% of the intervention group met the sustained-remission endpoint at 24 months against 21.2% of comparators. The confidence interval nearly touches no effect.
Household cure rates were 88.5 percent with permethrin against 71.8 percent with ivermectin. The trial set out to show ivermectin was non-inferior and found the opposite.
Germany's DINKS trial is one of the largest randomised tests of a reimbursable digital therapeutic. The effect is big, the comparator is usual care alone, and the sponsor made the app.
The headline finding is noninferiority. The more useful finding is what the shared denominator was — and how wide a gap the trial was designed to tolerate.
WISDOM randomised 28,372 women to annual mammography or a risk-tailored schedule. The risk-based arm met its non-inferiority mark for advanced cancers — with caveats about who enrolled.
A 240-woman randomised trial compared three months of hatha yoga with a time-matched conditioning programme. On every sleep measure, the two groups moved together.
An 18,476-person phase 3 trial and a small human challenge study landed the same day. Both favour the mRNA vaccine against influenza A; neither settles what it does against influenza B.
VESALIUS-CV randomised 12,257 patients with atherosclerosis or diabetes but no prior MI or stroke. Evolocumab reduced the three-point event rate from 8.0% to 6.2% over a median 4.6 years.
PISCES randomised 1,228 haemodialysis patients in Canada and Australia. The headline hazard ratio of 0.57 counts every event, not just the first — and that choice explains part of the gap.
The 162 mg group had 14.1% preterm or severe preeclampsia against 17.1% on 81 mg — a difference the trial could not distinguish from chance. Eight placental abruptions occurred on the higher dose and none on the lower.
The trial was designed to test non-inferiority against traditional dietary advice. It found superiority instead, with 62% versus 42% achieving a clinical response over six weeks.
In 311 adults aged 55 to 95, remission rates were 40% and 51% in the two intervention arms at one year, against 16% for online patient education. Adding human support helped a little.
In 270 patients whose voices persisted despite antipsychotics, the therapy beat matched clinical contact on hallucination severity by 2.26 points — significant, with a Cohen's d of 0.27.