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Chronic PainNCT05310747

Can Exposure to Inclusive Virtual Art Decrease Pain and Social Disconnection Among Individuals Living With Chronic Pain?

A study testing Artwork present, Artwork absent and Social connection high in people with Chronic Pain and Social Disconnection, run by University of California, Davis at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The proposed study is an experimental intervention to test for the effects of exposure to art by means of a virtual museum visit. It examines the fundamental question of whether exposure to virtual art can alleviate pain. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Chronic Pain, Social Disconnection
What is being tested?
Artwork present, Artwork absent and Social connection high
Could I receive a placebo?
No, everyone receives an active treatment
How many people
311 participants
Where
1 siteUnited States
Study dates
7 Oct 2022to 6 Jan 2023
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • read and write in English language
  • chronic moderate to severe pain (≥ 6 months in duration; ≥ 4 in response to the question, "on average this week my pain intensity has been?" on a 0-10 NRS)
  • lonely (≥ 4 on the 3-item Loneliness Scale)
  • access to an electronic device with internet connection in order to participate in the study

Who cannot join

  • dementia
  • adults unable to consent

Trial locations and contacts

1 site in 1 country.

United States1 site
  • University of California, Davis

    Sacramento, California, 95817

Other trials in United States

About this study

The proposed study is an experimental intervention to test for the effects of exposure to art by means of a virtual museum visit. It examines the fundamental question of whether exposure to virtual art can alleviate pain. Google Arts \& Culture has digitized the collections of over 2,000 museums, art galleries, and other cultural institutions. The platform is free and allows 'visitors' to explore art from around the world. For this study, the PIs have chosen artwork from this collection and created a virtual museum gallery such that research participants will visit the museum with or without art (i.e., we will remove all art from the virtual galleries). In addition, we hypothesize that individuals primed to experience social connection prior to art exposure will experience lower perceived social disconnection and pain than those who are not primed.

Read the detailed description

Research Design: 2 (virtual artwork exposure: present, absent) x 2 (prime: social connection prime: high, low) factorial experiment with a hanging control group (4 cells plus 1 control group, for a total of 5 cells) and 2 repeated measures. A priori power analysis using G*Power showed that the required sample size for a 5-group repeated measures experiment with 2 measurement times with 1-B error probability = .80 that expected small effect with a size of d = .10 and a significance level of p = .05 was a total of 305 participants (61 participants per cell).

Eligible individuals will be offered informed consent documentation via the StudyPages platform and then will be randomized to their study group:

  1. Artwork present + Social connection prime high
  2. Artwork present + Social connection prime low
  3. Artwork absent + Social connection prime high
  4. Artwork absent + Social connection prime low
  5. Hanging control group - no exposure to any independent variables (i.e. artwork: present or absent; social connection prime: high or low)

Participants will fill out pre-intervention scales (pain intensity and unpleasantness; perceived social disconnection) prior to their virtual museum experience. Participants will then visit a virtual art museum gallery for 10 minutes or receive no exposure if they are in the hanging control group. In the artwork present condition, the virtual museum will feature paintings as part of an exhibition. In the artwork absent condition, paintings will be removed and thus the virtual museum will be empty. In the high social connection prime condition participants will be assigned to write an essay about a person and situation that made them feel valued, seen, and heard. In the low social connection prime condition participants will be assigned to write about a person and situation that made them feel ignored and not very valued. After 10 minutes within their condition participants will complete a post-intervention survey.

In addition, written responses to the social connection primes and museum visit data (e.g., user movement, object interaction, and perceptions about artwork in the museum) will be collected and analyzed.

Being tested
Artwork present, Artwork absent, Social connection high, Social connection low
Keywords
Pain, Social Disconnection, Museum, Virtual museum
Medical subject headings
Chronic Pain, Pain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Artwork presentBehavioural

    A virtual museum exhibit with a curated selection of artworks

  • Artwork absentBehavioural

    The same virtual museum exhibit space as the 'Artwork present' condition but with all of the artworks removed from the walls

  • Social connection highBehavioural

    Participants will identify a person from their life that makes them feel socially connected and then write (1) about that person and (2) an experience they had with that person that made them feel socially connected.

  • Social connection lowBehavioural

    Participants will identify a person from their life that makes them feel socially disconnected and then write (1) about that person and (2) an experience they had with that person that made them feel socially disconnected.

Study groups in NCT05310747
Study groupRoleWhat they receive
Artwork present + social connection highExperimentalIndividuals participate in an exercise to prime a feeling of high social connection and then explore a virtual museum exhibit with artwork for 10 minutes
Receives: Behavioral: Artwork present; Behavioral: Social connection high
Artwork present + social connection lowExperimentalIndividuals participate in an exercise to prime a feeling of low social connection and then explore a virtual museum exhibit with artwork for 10 minutes
Receives: Behavioral: Artwork present; Behavioral: Social connection low
Artwork absent + social connection highExperimentalIndividuals participate in an exercise to prime a feeling of high social connection and then explore a virtual museum exhibit with no artwork for 10 minutes
Receives: Behavioral: Artwork absent; Behavioral: Social connection high
Artwork absent + social connection lowActive comparatorIndividuals participate in an exercise to prime a feeling of low social connection and then explore a virtual museum exhibit with no artwork for 10 minutes
Receives: Behavioral: Artwork absent; Behavioral: Social connection low
Hanging control groupNo interventionIndividuals will receive no exposure to any independent variables (i.e. artwork: present or absent; social connection prime: high or low) for 10 minutes before completing their final survey.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Social disconnection

    Social disconnection scale; 12 items; scored 1 (not at all) - 5 (very much); range 12-60

    Measured: Post-intervention (immediately)/Day 1

Secondary outcomes (8)
  1. Pain unpleasantness

    Numerical rating scale (NRS) score of 0 "not unpleasant" - 10 "Most unpleasant sensation imaginable ("intolerable")"

    Measured: Post-intervention (immediately)/Day 1

  2. Pain intensity

    Numerical rating scale (NRS) score of 0 "no pain" - 10 "worst pain imaginable"

    Measured: Post-intervention (immediately)/Day 1

  3. Change in pain during intervention

    Did you experience any pain relief during the museum experience? 1=Yes/0=No

    Measured: Post-intervention (immediately)/Day 1

  4. Percent change in pain during intervention

    If "Yes", what percent pain relief did you receive? 0%-100%

    Measured: Post-intervention (immediately)/Day 1

  5. Perceptions of the artwork related to the positivity of the social world

    The artwork in the museum made me feel (7-point likert scale anchored by "Negative about the social world" and "Positive about the social world")

    Measured: Post-intervention (immediately)/Day 1

  6. Perceptions of the artwork related to connection to the social world

    The artwork in the museum made me feel (7-point likert scale anchored by "Disconnected to the social world" and "Connected to the social world")

    Measured: Post-intervention (immediately)/Day 1

  7. Perceptions of the artwork related to inclusion in the social world

    The artwork in the museum made me feel (7-point likert scale anchored by "Excluded from the social world" and "Included in the social world")

    Measured: Post-intervention (immediately)/Day 1

  8. Perceptions of the artwork related to positivity of social relationships

    The artwork in the museum made me feel (7-point likert scale anchored by "Negative about my social relationships" and "Positive about my social relationships"

    Measured: Post-intervention (immediately)/Day 1

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 Apr 2022
  2. Study start7 Oct 2022
  3. Primary completion6 Jan 2023
  4. Study completion6 Jan 2023

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Factorial
Model description
Eligible individuals will be randomized to one of 4 groups: 1. Artwork present + Social connection prime high 2. Artwork present + Social connection prime low 3. Artwork absent + Social connection prime high 4. Artwork absent + Social connection prime low 5. Hanging control group - no exposure to any independent variables (i.e. artwork: present or absent; social connection prime: high or low)
Masking
Triple blind
Who is masked
Participant, Investigator, Outcomes assessor
Enrolment
311 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05310747
Sponsor's protocol ID
1811205
Status last verified
Apr 2025
First submitted
16 Dec 2021
Last updated
23 Apr 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Artwork present, Artwork absent and Social connection high in people with Chronic Pain and Social Disconnection, run by University of California, Davis at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 23 Apr 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Social disconnection (time frame: Post-intervention (immediately)/Day 1). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 Apr 2025.

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