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Recruiting NCT05540106

NCT05540106 Impact of Art Therapy on Self-Reported Pain and Anxiety Scores of Patients Waiting to Be Seen in the Emergency Department

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Clinical Trial Summary
NCT ID NCT05540106
Status Recruiting
Phase
Sponsor Stony Brook University
Condition Anxiety
Study Type INTERVENTIONAL
Enrollment 168 participants
Start Date 2023-08-01
Primary Completion 2026-12-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
All Conditions
Interventions
Nature Coloring PacketGeometric Shape Coloring PacketActivity Book

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 168 participants in total. It began in 2023-08-01 with a primary completion date of 2026-12-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The objective of this research is to assess the effects of engaging in coloring activities on patients' self-reported pain and anxiety scores while they wait to be seen by a physician in an emergency department (ED). The current literature on patient visits in the ED highlights the significance of anxiety, stress, and frustration in patient experiences, especially when accounting for long wait times before the physician-patient encounter. The study will address this common problem by looking at the potential impact of nature-themed or geometric shape coloring activities on the ED patient experience as it relates to self-reported anxiety and pain scores. Given that long wait times are increasingly being reported across the country, this study may offer a possible meaningful low-budget, low-resource intervention which could be offered to patients.

Eligibility Criteria

Inclusion Criteria: * Triage Pain Score \> 3 * Age \>18 * Able to provide informed consent * English-speaking * without concern for aggressive behavior * Glasgow Coma Scale (GCS) of 15 * Hospital Anxiety and Depression Scale-Anxiety (HADS-A) Score \> 6 Exclusion Criteria: * Concern for aggression risk, including active concern for suicidal or homicidal ideations * Glasgow Coma Scale (GCS) \<15 * triage acuity requiring critical care evaluation

Contact & Investigator

Central Contact

Lauren M Maloney, MD

✉ lauren.maloney@stonybrookmedicine.edu

📞 631-358-6652

Frequently Asked Questions

Who can join the NCT05540106 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Anxiety. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT05540106 currently recruiting?

Yes, NCT05540106 is actively recruiting participants. Contact the research team at lauren.maloney@stonybrookmedicine.edu for enrollment information.

Where is the NCT05540106 trial being conducted?

This trial is being conducted at Stony Brook, United States.

Who is sponsoring the NCT05540106 clinical trial?

NCT05540106 is sponsored by Stony Brook University. The trial plans to enroll 168 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology