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NCT06072859Completed

The Impact of Simulated Forest Immersion Therapy on Pain and Anxiety in Patients Axial Spondyloarthritis (axSpA)

Source: ClinicalTrials.gov · Last updated 31 Jul 2025

Brief summary (registry, in English)

The purpose of the study is to learn about the ease of using a humidified fragrant citrus forest oil, along with a virtual simulation of a forest environment (i.e., with sights and sounds of nature using a personal tablet Surface Pro 3 with headphones, to learn more about how these two aspects of the simulated forest immersion therapy (SFIT) may improve pain, anxiety, blood-pressure, and heart rate related to Axial Spondyloarthritis. The investigators hope to learn how well SFIT may impact pain levels, feelings of calm, as well as blood- pressure and heart rate, and how participants tolerate the experience overall.

Status (registry)
Completed
Study type
Interventional
Enrollment
10 (actual)
First submitted
26 Sept 2023
Start date
21 Sept 2023
Primary completion date
31 Mar 2024
Lead sponsor
Oregon Health and Science University
NCT number
NCT06072859

What you commit to

  • Study type: Interventional
  • Participants enrolled: 10
  • From 21 Sept 2023 to the primary completion date, 31 Mar 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • history of asthma
  • known allergy to citrus aroma
  • history of hypertension uncontrolled by medications

Other

  • currently pregnant
  • inability to detect common odors from commercial fragrances
  • smoking within 15 minutes of the start of the intervention procedure
  • hard of hearing without assistive devices
  • limited vision not corrected by eye lenses

Who the study is looking for

  • able to read at a 5th grad level
  • medically diagnosed with Axial Spondyloarthritis
  • tolerate having their BP and HR taken
  • average of greater than 3 on their last recorded pain assessments
  • average of greater than 4 on their last BASDI recorded
  • currently have an assigned Rheumatologist in their care delivery

Age in the registry: 18 years to 100 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Oregon Health Science University
Coordinator of this site? Confirm its status
PortlandUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.