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After an initial phone screen process, approximately 50 participants will be enrolled and evaluated/screened in person after consenting to achieve 30 eligible participants with a principal diagnosis of GAD, panic disorder, or social anxiety disorder and high anxiety sensitivity (Anxiety Sensitivity Index score =20). Participants will be given a choice of either high intensity interval training (HIIT) or walking interventions, which will be completed over the course of 8 weeks. The goal of the study is to 1) obtain pilot data comparing the efficacy of HIIT vs. walking for effects on psychiatric, functioning and immune outcomes, 2) to identify adherence levels given the choice of exercise intensity, and 3) to identify proportion of individuals opting for each intervention. Results from this pilot study will be used to inform future grant applications including a K award.
Age
18 - 65 years
Sex
ALL
Healthy Volunteers
No
NYU Langone
New York, New York, United States
Start Date
December 11, 2018
Primary Completion Date
July 29, 2020
Completion Date
July 29, 2020
Last Updated
September 28, 2020
9
ACTUAL participants
Low Intensity Exercise Intervention
BEHAVIORAL
High Intensity Intervention
BEHAVIORAL
Lead Sponsor
NYU Langone Health
NCT07456631
NCT07429578
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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