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Emotional and Affective Responses to Music Inspired by Permafrost Thaw in Nunavik

NCT07915089, Not applicable, Not yet recruiting, Centre integre universitaire de sante et de services sociaux du Centre-Sud-de-l'Île-de-Montréal

Trial 10

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

FieldValueSource
TitleEmotional and Affective Responses to Music Inspired by Permafrost Thaw in NunavikClinicalTrials.gov
NCT numberNCT07915089ClinicalTrials.gov
StatusNot yet recruitingClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment80 participants, estimatedClinicalTrials.gov
Lead sponsorCentre integre universitaire de sante et de services sociaux du Centre-Sud-de-l'Île-de-MontréalClinicalTrials.gov
ConditionsEmotion, Affective Response, Physiological ResponsesClinicalTrials.gov
InterventionsViewing Four Audiovisual Artworks Inspired by Environmental Changes in NunavikClinicalTrials.gov
First posted2026-11-04ClinicalTrials.gov
Last updated2026-11-06ClinicalTrials.gov

Registered outcomes 7

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescriptionSource
PrimaryChange in Affect Grid Valence Score Following Each Audiovisual ArtworkImmediately before and after each 3-minute-50-second artwork during one approximately 60-minute laboratory session.
Emotional valence is assessed using the horizontal coordinate of the Affect Grid, ranging from 1 (unpleasant) to 9 (pleasant). For each artwork, change is calculated as the score immediately after viewing minus the score immediately before viewing. Positive changes indicate greater pleasantness. Responses are compared across the four artworks within participants.
ClinicalTrials.gov
PrimaryChange in Affect Grid Arousal Score Following Each Audiovisual ArtworkImmediately before and after each 3-minute-50-second artwork during one approximately 60-minute laboratory session.
Subjective arousal is assessed using the vertical coordinate of the Affect Grid, ranging from 1 (low arousal) to 9 (high arousal). For each artwork, change is calculated as the score immediately after viewing minus the score immediately before viewing. Positive changes indicate greater subjective activation. Responses are compared across the four artworks within participants.
ClinicalTrials.gov
PrimaryElectrodermal Responses During Audiovisual Artwork ViewingDuring the approximately one-minute rest before each artwork and throughout each 3-minute-50-second presentation, within one approximately 60-minute session.
Electrodermal activity is recorded continuously using the Shimmer3 GSR+ device. Tonic skin conductance level and phasic skin conductance responses characterise physiological activation during each artwork. Recordings are evaluated relative to the approximately one-minute resting period preceding each artwork and compared across the four artworks within participants. Skin conductance is expressed in microsiemens; higher activity does not identify whether an emotion is positive or negative.
ClinicalTrials.gov
PrimaryHeart Rate Responses During Audiovisual Artwork ViewingDuring the approximately one-minute rest before each artwork and throughout each 3-minute-50-second presentation, within one approximately 60-minute session.
Heart rate is estimated from the photoplethysmographic pulse signal recorded using the Shimmer3 GSR+ device and expressed in beats per minute. Responses during each artwork are evaluated relative to the preceding approximately one-minute resting period and compared across the four artworks within participants.
ClinicalTrials.gov
SecondaryChange in Global Affective Polarity Following Each Audiovisual ArtworkImmediately before and after each 3-minute-50-second artwork during one approximately 60-minute laboratory session.
Global Affective Polarity (GAP) is a study-developed exploratory composite based on six items rated from 0 to 10. GAP-P is the mean of pleasantness, joy and appeasement; GAP-N is the mean of unpleasantness, sadness and melancholy. Global GAP equals GAP-P minus GAP-N and ranges from -10 to +10. Higher scores indicate predominance of positive affective components. Component scores each range from 0 to 10. Changes are calculated separately for each artwork as post-viewing minus pre-viewing scores.
ClinicalTrials.gov
SecondaryChange in Nature Connection Index ScoreAt inclusion before the laboratory visit and immediately after viewing all four artworks during the approximately 60-minute laboratory session.
Nature connectedness is assessed using the six-item Nature Connection Index. Responses are recorded on seven-point agreement scales and coded so that higher values indicate stronger connectedness. Under the study protocol, the mean item score is transformed to a 0-100 index using \[(mean score - 1)/6\] × 100. Higher scores indicate greater nature connectedness. Change is calculated as the score after viewing all four artworks minus the score collected at inclusion.
ClinicalTrials.gov
SecondaryChange in Hogg Eco-Anxiety Scale ScoreAt inclusion before the laboratory visit and immediately after viewing all four artworks during the approximately 60-minute laboratory session.
Eco-anxiety is assessed using the 13-item Hogg Eco-Anxiety Scale (HEAS-13). Items are rated from 0 to 3 and summed to produce a total score ranging from 0 to 39. Higher scores indicate more frequent eco-anxiety-related responses. Change is calculated as the score after viewing all four artworks minus the score collected at inclusion. This exploratory assessment does not imply that the artworks constitute a treatment for eco-anxiety.
ClinicalTrials.gov

Outcomes 0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured asSource

Results by group 0

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnitsSource

Participant flow 0

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits countedSource

Adverse events 0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEventsSource

Adverse event totals 0

The totals the trial posted for each group.

TotalGroupAffectedAt riskSource

Papers 0

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource

Grants 0

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.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal yearsSource

Trial comparisons 0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource

Tests 0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

TestNamed asSource

Source 5

FieldValueSource
Releasetrials-2026-11-12-0.4.0ClinicalTrials.gov
Release manifest SHA-2560f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4ClinicalTrials.gov
Registry capture2026-11-12ClinicalTrials.gov
Results copy, AACT2026-03-23ClinicalTrials.gov
NIH clinical studies file2026-11-13ClinicalTrials.gov

The same record as JSON

Release trials-2026-11-12-0.4.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)