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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03153891
Other study ID # 1703006971
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 1, 2016
Est. completion date June 2018

Study information

Verified date March 2019
Source Cornell University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This randomized controlled trial examines the effect of nature exposure on pain intensity levels among older adults who experience chronic pain. Investigators examine the effects of nature on: the experience of chronic pain, on pain catastrophizing, and on attention restoration.


Description:

Nature has been used to reduce pain in the context of acute pain (e.g., during painful medical procedures) but nature has not been examined as an intervention strategy to address chronic pain. Second, the mechanism though which nature might reduce the experience of pain is not well understood. Participants are cognitively intact individuals aged 60-90 who experience chronic pain and who rate their health as fair, good or excellent. Participants are randomly assigned to one of three conditions: virtual reality (VR) nature; VR built environment; or control. Researchers examine effects of VR nature exposure on the experience of chronic pain, pain catastrophizing, and on attention restoration as well as the relations among these variables.


Recruitment information / eligibility

Status Completed
Enrollment 23
Est. completion date June 2018
Est. primary completion date June 2018
Accepts healthy volunteers No
Gender All
Age group 60 Years to 90 Years
Eligibility Inclusion Criteria:

- rate health as "fair" "good" or "excellent"

- experience chronic pain

- cognitively intact

- do not use wheelchair

Exclusion Criteria:

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Natural Environment
the natural environment will be delivered via Samsung VR gear goggles with Samsung smartphone.
Built Environment
the built environment will be delivered via Samsung VR gear goggles with Samsung smartphone.

Locations

Country Name City State
United States Cornell University Ithaca New York

Sponsors (1)

Lead Sponsor Collaborator
Cornell University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Experience of chronic pain rating of pain intensity, on scale of 1-10 up to 3 weeks; from date of randomization until 2nd data collection date
Secondary Pain catastrophizing rate 13 items on 5-point scale (0-4) (Sullivan, et al., 2001) up to 3 weeks; from date of randomization until 2nd data collection date
Secondary cognitive functioning attention restoration - digit span forward & backwards; Attention Network Test up to 3 weeks; from date of randomization until 2nd data collection date
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