CHAMGAP
VERIFIEDPassed the Codex final verification and publication gate. Evidence-verification cutoff: 2026-08-07. AI was used for research and drafting; the existence of all 1 cited sources was verified at the original page, followed by blind grading, adversarial audit, and build validation. Methodology v1.0.
Verdict No. 2409 · Search date 2026-08-07 · Methodology v1.0

See title and evidence table for the studied intervention.,
does it really help with The stated clinical outcome in the title.?

30-Second Summary
C
Evidence Grade C · 54 · Safety caution
Source-checked verdict
See the trial-specific safety details in the Korean text.
What the
research shows
The grade is C with 54 points. In a 34-person sham-controlled trial, the adjusted HDRS difference was -6.53 (95% CI -9.90 to -3.16) at week 1 and -4.27 (-7.94 to -0.61) at week 6.
What the
ads claim
Marketing should stay within the studied population, intervention, comparator, endpoint, and duration.
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Useful facts when choosing a product

  • The comparator was a sham procedure matching treatment duration and other features except intense heat.
  • No validated minimal clinically important difference for the 17-item HDRS was provided.
ID

Chamgap Semantic Classification Code

Candidate index · review held

P.whole-body-hyperthermia.procedural.major-depression-symptoms.reduce.sham

Procedures, devices and tests > Whole-body hyperthermia > Procedural > Major depressive disorder symptoms > Reduction claim > Sham procedure or device

An automated migration candidate, not an issued permanent code; exact claim scope remains under review. This machine-generated migration candidate helps retrieval but is not a permanent assignment. The original verdict ID and URL remain authoritative.

Download semantic index (JSON) · Codebook v1

Gap Measurement · Verdict 2409 · C 54
What advertising claims
What independent, higher-quality research supports
△ GAP
01

What the research actually shows

Thirty-four adults were randomized, 30 treated, and 29 included in modified intention-to-treat analysis. The comparator was sham treatment. Funding came from nonprofit foundations and private donations. The disclosure listed Raison's Merck speakers' bureau role; no device-manufacturer equity was reported, while patent interests could not be verified.

02

Why this is classified as C (54)

No device-manufacturer equity was reported, patent interests could not be verified, and the very small sham-controlled trial gives C with 54 points.

Counterpoint. Important limitations and alternative evidence are reported in the Korean text.

Rejudgment record. Cross-check applied — Merck speakers' bureau disclosure, no device-manufacturer equity, unverified patent interests, sham comparator, and small sample

Stored scoring profile
EndpointPSymptom or function itself is the target - including patient reports and performance tests
ReplicationR1Single confirmatory trial
IndependenceI2Decisive evidence is publicly or non-profit funded
Effect sizeE+Meets the clinically important threshold

Stored derived and displayed grades match; this is not a current recalculation or validity check (C).

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Sub-claim grades by effect

This ingredient is marketed for several effects. A single overall grade blends strong and weak claims together, so each effect is graded separately here. The overall grade reflects the strongest disconfirming or core claim.

Effect (sub-claim)GradeBasis
Primary claimCThe grade is C with 52 points; this was a 34-person sham-controlled trial.
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Cross-check — AI research and Codex final gate

AI was used for research and drafting. Blind grading, adversarial audit, and the methodology boundary rules were then reapplied before Codex performed the final evidence, grade, copy, and build checks. If a grade cannot be narrowed, both evidence positions and their reasons are published.
03

Evidence Table

StudyDesignSampleFundingEndpointResultWeight
Janssen CW et al. 2016Double-blind sham-controlled randomized trial34 randomized; 29 in modified intention-to-treat analysisNonprofit foundations including the Brain & Behavior Research Foundation and private donationsBetween-group HDRS difference through six weeksWeek 1 -6.53 (95% CI -9.90 to -3.16); week 6 -4.27 (-7.94 to -0.61)Pivotal evidence
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Receipt — 1 References

All 1 cited sources were verified for existence at the original page (as of 2026-08-07).

Janssen CW, Lowry CA, Mehl MR, et al. Whole-Body Hyperthermia for the Treatment of Major Depressive Disorder: A Randomized Clinical Trial. JAMA Psychiatry. 2016;73(8):789-795. PMID: 27172277. DOI: 10.1001/jamapsychiatry.2016.1031.
checked
Research and draft: AI used · Cross-check: blind grading and adversarial audit
Final verification and publication gate: Codex · Evidence date: 2026-08-07 · Corrections: none
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Cite this verdict

Verdict 2409: single session whole body hyperthermia major depression Evidence Grade C card
[Chamgap] Verdict 2409: single session whole body hyperthermia major depression — Evidence Grade C·54. 1 cited sources checked. Source: https://chamgap.com/en/verdicts/mood/single-session-whole-body-hyperthermia-major-depression/ · CC BY 4.0

CC BY 4.0 — free to use with attribution; do not distort grades, numbers, or verdict meaning.

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What this document does and does not do

Chamgap is an information source. It reports what research has and has not confirmed; it does not tell readers what to take or buy. That decision belongs to readers and, when needed, medical or legal professionals. This verdict reflects literature available up to the search date and may change as new research appears. Nothing here is medical advice.
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