Art-based Beauty Appreciation Intervention

NCT06788496 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 114

Last updated 2025-08-17

No results posted yet for this study

Summary

This study is a randomized controlled trial with an active control condition evaluating the impact of an art-based beauty appreciation (ABBA) intervention on trait appreciation of beauty as a primary outcome and well-being and psychological distress as secondary outcomes. The central hypothesis is that the primary and secondary outcomes will increase more in the intervention than in the control condition.

Conditions

  • Young Adults
  • Sensory Processing Sensitivity

Interventions

BEHAVIORAL

Art-based Beauty Appreciation Intervention Program (Learning to See Beauty)

The goals of the intervention program are to help individuals develop an aesthetic mindset, practice observation and appreciation skills, learn how to apply these skills to their day-to-day lives, practice emotion regulation with beauty, and incorporate more beauty into their lives. The program is designed to create a slow skill transfer from appreciation in art contexts to natural beauty and to everyday life. In the 14-day program, participants visit an art museum with guided audio, watch instructional videos about observing and appreciating beauty, and complete daily written or photo beauty journals that document the beauty they see. In addition, participants will watch video art showing how to find beauty in mundane objects, practice this in a beauty walk, and complete a planning session to include more beauty in their lives.

BEHAVIORAL

Observation Program (Learning to Observe Life)

The active, matched control group will focus on developing pragmatic observation skills. Participants will be instructed to pay attention to and identify objects and elements in their surroundings without emphasizing their aesthetic value. For example, they should pay attention and count objects of the same colour they encounter, social behaviour, the people they pass on the street, or the types of buildings. The 14-day program includes a tourist trip with guided audio instruction, watching instructional videos about increasing observation skills and completing daily written or photo journals to document their observations. Further, participants will take an observation walk and plan to include more observation in their lives.

Sponsors & Collaborators

  • University of Amsterdam

    collaborator OTHER
  • University of Vienna

    collaborator OTHER
  • Radboud University Medical Center

    lead OTHER

Principal Investigators

  • MacKenzie D Trupp, PhD Candidate · RadboudUMC, Donders Institute for Brain, Cognition and Behaviour and University of Vienna

  • Corina Greven, Prof. Dr. · RadboudUMC, Donders Institute for Brain, Cognition and Behaviour

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
28 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-11-22
Primary Completion
2025-07-18
Completion
2025-07-18

Countries

  • Netherlands

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06788496 on ClinicalTrials.gov