ClinicalTrials.Veeva

Menu

Effect of Environment on the Central and Peripheral Nervous System (RUMI)

University of South Florida logo

University of South Florida

Status

Invitation-only

Conditions

Rumination

Treatments

Other: Built environment
Other: Natural environment

Study type

Interventional

Funder types

Other

Identifiers

NCT06778356
STUDY007343

Details and patient eligibility

About

The main goal of this study is to understand how different environments influence both mental responses, like overthinking (rumination), and physical reactions, such as heart rate and blood pressure, after a challenging task.

Full description

This study aims to explore the restorative effects of nature exposure on rumination- a mental process that affects attention-and cardiovascular responses to a challenging task. A total of 95 participants will be randomly assigned to either a built or natural environment. Each participant will take part in a 2.5-hour session. Initially, an electrocardiogram (ECG) will be attached to measure heart activity. Participants will then engage in a 30-minute task designed to immerse them in their assigned environment (the ABC engagement task). Following this, they will have a 10-minute period of quiet relaxation to establish baseline cardiovascular measures. After baseline, participants will complete a challenging task (the Remote Associates Test (RAT)), which is designed to induce sympathetic arousal. Afterward, they will rest quietly for another 10 minutes to monitor cardiovascular recovery. Finally, participants will complete post-task surveys through Qualtrics, assessing their state of rumination, perceived difficulty of the task, effort levels, and expectations of success.

Enrollment

95 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Individuals 18 years of age or older.

Exclusion criteria

  • Individuals with a history of cardiovascular disease or disorders, those who are pregnant, or are taking medications which may alter/affect cardiovascular function.

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

95 participants in 2 patient groups

Built environment assignment
Experimental group
Description:
Participants will complete the study session in a built environment
Treatment:
Other: Built environment
Natural environment
Experimental group
Description:
Participants will complete the study session in a natural environment.
Treatment:
Other: Natural environment

Trial contacts and locations

1

Loading...

Central trial contact

Susan S Rodriguez, Bachelor of Arts; Michael Hopkins, Bachelor of Arts

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems