ClinicalTrials.gg
Not yet recruitingNCT07915089Updated Nov 6, 2026

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

An interventional study of Viewing Four Audiovisual Artworks Inspired by Environmental Changes in Nunavik in Emotion, Affective Response and Physiological Responses, sponsored by Centre integre universitaire de sante et de services sociaux du Centre-Sud-de-l'Île-de-Montréal. Not yet recruiting at 1 site in Canada. Open to participants aged 18 Years to 35 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-11-06.

Sponsored by Centre integre universitaire de sante et de services sociaux du Centre-Sud-de-l'Île-de-Montréal · Not applicable, Interventional, and Other

Updated Nov 4, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
80
Allocation
Not applicable
Ages
18 Years to 35 Years
Sex
All
01

Study summary

This study will compare how young adults respond to four audiovisual artworks inspired by ice melt and permafrost thaw in Nunavik, northern Quebec. Permafrost is ground that remains frozen for at least two consecutive years. The researchers want to understand whether the artworks evoke different emotions, bodily responses and personal interpretations, and whether they help make environmental changes more concrete and meaningful.

The four artworks draw on the same 30 years of environmental data from the Tasiujaq area of Nunavik. They combine music and moving images through different creative approaches:

  1. Contemporary music created by a human composer, paired with images generated using artificial intelligence (AI).
  2. Inuit pop-rock music created independently by an Inuk artist, paired with AI-generated images.
  3. Music and images generated using AI from the environmental data.
  4. AI-generated music combining and reworking material from the two human-created compositions, paired with AI-generated images.

The study will recruit 80 adults aged 18-35 who understand French or English and can provide informed consent. It will take place at the Research Centre of the Montreal Geriatric University Institute in Montreal, Quebec, Canada.

Before attending, participants will complete approximately 30 minutes of online questionnaires about their background, connection with nature, environmental concerns, and familiarity with music, Inuit culture, Nunavik and AI. They will then attend one laboratory session lasting approximately 60 minutes.

During the session, every participant will watch and listen to all four artworks. Each artwork lasts 3 minutes and 50 seconds. Participants will be assigned to one of eight presentation orders to reduce the influence of viewing order on their responses. Viewing conditions will be kept consistent, and the artworks will be presented under neutral labels.

Before each artwork, participants will sit quietly for approximately one minute while resting physiological measurements are recorded. Sensors will measure changes in skin conductance, which reflects changes in sweating, and heart rate during viewing. These measurements will be considered alongside participants' own reports because they cannot, by themselves, identify a specific emotion.

Participants will complete short questionnaires before and after each artwork about how pleasant or unpleasant they feel, how calm or activated they feel, and specific positive and negative emotions. Further questions will explore their appreciation and interpretation of the artworks and the responses the works evoke. After viewing all four, participants will repeat questionnaires about nature connectedness and environmental anxiety, compare the artworks, and explain their choices in their own words.

The researchers will compare responses to the four artworks within each participant and explore whether responses are associated with individual characteristics, including initial environmental concerns and familiarity with the arts or AI. Each artwork will be evaluated as a complete experience. Differences cannot be attributed separately to musical style, cultural references or the use of AI.

This study is not a treatment for anxiety or another health condition, and no direct health benefit is guaranteed. Participants may request a break or stop the session at any time.

02

Conditions studied

  • Emotion
  • Affective Response
  • Physiological Responses
03

In context

Lead sponsor

Centre integre universitaire de sante et de services sociaux du Centre-Sud-de-l'Île-de-Montréal is the lead sponsor of 13 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 35 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Aged 18-35 years.
  • Able to understand French or English, according to the language used for the questionnaires and .
  • Able to provide free and informed consent.

Exclusion criteria

Exclusion Criteria:

  • Unable to understand the study instructions or provide free and .
  • Major uncorrected visual or hearing impairment preventing adequate viewing or listening to the artworks.
  • Anticipated substantial discomfort when viewing content about climate change, ice melt, permafrost thaw or environmental changes in northern regions.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
80 participants (estimated)

Study arms

  • Experimental
    Exposure to Four Nunavik-Inspired Audiovisual Artworks

    Participants watch and listen to four audiovisual artworks inspired by ice melt and permafrost thaw in Nunavik during one laboratory session. Each artwork lasts 3 minutes and 50 seconds. All participants experience all four artworks, which combine human-created or AI-generated music with AI-generated images. Questionnaires assess emotional and affective responses before and after each artwork. Skin conductance and heart rate are recorded during viewing. Participants also evaluate and compare the artworks and describe their interpretations.

    Other: Viewing Four Audiovisual Artworks Inspired by Environmental Changes in Nunavik

Interventions

  • OtherViewing Four Audiovisual Artworks Inspired by Environmental Changes in Nunavik

    Participants attend one laboratory session and view four audiovisual artworks inspired by 30 years of data on ice melt and permafrost thaw in Nunavik. Each artwork lasts 3 minutes and 50 seconds. Two combine independently human-composed music with AI-generated images. A third combines AI-generated music and images based on the environmental data. A fourth combines AI-generated images with music created by merging and reworking the two human compositions. All participants experience all four artworks under standardised viewing and listening conditions. Each presentation is preceded by approximately one minute of quiet rest and followed by a questionnaire period.

06

What researchers measure

Primary outcomes

  1. Change in Affect Grid Valence Score Following Each Audiovisual Artwork

    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.

    Time frame: Immediately before and after each 3-minute-50-second artwork during one approximately 60-minute laboratory session.

  2. Change in Affect Grid Arousal Score Following Each Audiovisual Artwork

    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.

    Time frame: Immediately before and after each 3-minute-50-second artwork during one approximately 60-minute laboratory session.

  3. Electrodermal Responses During Audiovisual Artwork Viewing

    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.

    Time frame: During the approximately one-minute rest before each artwork and throughout each 3-minute-50-second presentation, within one approximately 60-minute session.

  4. Heart Rate Responses During Audiovisual Artwork Viewing

    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.

    Time frame: During the approximately one-minute rest before each artwork and throughout each 3-minute-50-second presentation, within one approximately 60-minute session.

Secondary outcomes

  1. Change in Global Affective Polarity Following Each Audiovisual Artwork

    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.

    Time frame: Immediately before and after each 3-minute-50-second artwork during one approximately 60-minute laboratory session.

  2. Change in Nature Connection Index Score

    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.

    Time frame: At inclusion before the laboratory visit and immediately after viewing all four artworks during the approximately 60-minute laboratory session.

  3. Change in Hogg Eco-Anxiety Scale Score

    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.

    Time frame: At inclusion before the laboratory visit and immediately after viewing all four artworks during the approximately 60-minute laboratory session.

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

2 registry updates since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Nov 4, 2026
Show all 2 updates
  1. Nov 6, 2026
    Minor edits only
    + 2 other changes: verification date and conditions
  2. Nov 4, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07915089
Lead sponsor
Centre integre universitaire de sante et de services sociaux du Centre-Sud-de-l'Île-de-Montréal
Responsible party
Olivier Beauchet (MD, PhD, Centre integre universitaire de sante et de services sociaux du Centre-Sud-de-l'Île-de-Montréal) — Principal investigator
First posted
Nov 4, 2026
Start date
Nov 1, 2026 (estimated)
Primary completion
Mar 30, 2027 (estimated)
Completion
Mar 30, 2027 (estimated)
Last update
Nov 6, 2026

Study contacts

Olivier Beauchet, MD, PhD
Contact
olivier.beauchet@umontreal.ca
514 340 3540 ext. 3637
Kevin Galery, MSc
Contact
kevin.galery.ccsmtl@ssss.gouv.qc.ca
514 340 3540 ext. 4728

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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