Trial · NCT07903896
Heat and Mental Health - PART 2
NCT07903896, Not applicable, Recruiting, Hartford Hospital
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Heat and Mental Health - PART 2. Trials, record NCT07903896. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07903896
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Heat and Mental Health - PART 2
- NCT number
- NCT07903896
- Status
- Recruiting
- Phases
- Not applicable
- Enrollment
- 75 participants, estimated
- Lead sponsor
- Hartford Hospital
- Conditions
- Depressed Mood, Young Adults, Heat Stress, Sleep
- Interventions
- Heat/Humidity Exposure Condition, Thermoneutral Condition
- First posted
- 2026-10-29
- Last updated
- 2026-10-29
Source ClinicalTrials.gov
Registered outcomes14
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | PANAS-10 | periprocedurally* measures collected during lab weekends (i.e. periprocedurally) ONLY - marked with " * " | EMA Mood 10 items 5-pt Likert Score: 10-50 |
| Primary | POMS-8 [depression subscale of POMS-60] | periprocedurally* | EMA Depressed Mood 8 items 5-pt Likert Score: 0-32 |
| Primary | PHQ-9 | baseline, pre-intervention, periprocedurally | EMA Depressed Mood 9 items 4-pt Likert Score: 0-27 |
| Primary | GAD-7 | baseline, pre-intervention, periprocedurally | EMA Anxious Mood 7 items 4-pt Likert Score: 0-21 |
| Primary | Qualitative Experience | immediately after intervention* | In-person interview |
| Secondary | Sleep Self Assessment | pre-intervention, periprocedurally | Audio-diary |
| Secondary | Sleep Monitoring | pre-intervention, periprocedurally | i) Sleep Stages (times, duration) - est. from Heart Rate (BPM) + Movement. Stages = Light, Deep, REM ii) Time Asleep \& Time in Bed iii) Time Awake \& Restlessness |
| Secondary | 18-channel attended polysomnography (PSG) | periprocedurally* | i) EEG (32-channel, 10-20 system) Sleep stage distribution: N1, N2, N3, REM (% and minutes per stage) Total Sleep Time (TST) Sleep Onset Latency (SOL) REM Latency Wake After Sleep Onset (WASO) Sleep Efficiency (TST / Time in Bed) Number of awakenings Arousal Index (EEG-defined arousals/hour, AASM criteria) Spontaneous (non-respiratory, non-limb) arousal count ii) EOG REM density iii) Submental EMG Atonia confirmation for REM staging Chin EMG tone, used jointly with EEG/EOG for arousal scoring iv) Bilateral anterior tibialis EMG Periodic Limb Movement Index (PLMI; events/hour) PLM Arousal Index (PLM events assoc. EEG arousal) v) ECG Heart Rate \& Variability across sleep stages vi) Nasal pressure + oronasal thermal airflow AHI vii) Thoracic + abdominal respiratory effort belt Obstructive vs. central, RERA → RDI viii) Pulse oximetry SpO2 nadir ODI, ≥3% or ≥4% threshold %TST \< 90% ix) Snore sensor * TST snoring x) Body position sensor T/pos (supine, lateral, prone) Pos-dependent AHI |
| Secondary | Actigraphy | pre-intervention, periprocedurally | i) Steps/day ii) Distance/day iii) Heart rate (BPM) |
| Secondary | Flanker Task | pre-intervention, periprocedurally | EMA i) Reaction Time (RT) Mean/median RT (ms) / trial type x Congruent v. Incongruent trials Flanker Effect (or interference effect) = RT(incongruent) - RT(congruent) ii) Accuracy % correct x Congruent v. Incongruent Accuracy Interference Effect = accuracy(congruent) - accuracy(incongruent) |
1 to 10 of 14Source ClinicalTrials.gov
See all 14 registered outcomesOutcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers8
The papers the trial lists on ClinicalTrials.gov.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests3
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|---|---|
| 2-Back Task | Secondary outcome | ConductCognition |
| Eriksen Flanker Task | Secondary outcome | ConductCognition |
| Oddball Target Detection | Other outcome | ConductCognition |
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07903896
GET https://conductscience.org/api/trials/v1/NCT07903896/registered