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NCT04292145 Clinical Trial

Effectiveness of Relaxation Techniques

Stress, Psychological Clinical Trial

Official title:
Efficacy of an Application as a Relaxation Technique

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT04292145
Other study ID # H19-130-MEUA
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date April 22, 2020
Est. completion date December 22, 2024

Study information
Verified date April 2024
Source Southern Methodist University
Contact Richard Y Kim, BA
Phone 214-768-1291
Email richardk@smu.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study aims to assess the validity of a relaxation app. This will be accomplished by obtaining self-report measures about mood and respiratory symptoms. We hypothesize that self-report in the relaxation app condition will be different from that of the relaxation only condition.

Recruitment information / eligibility
Status Recruiting
Enrollment 100
Est. completion date December 22, 2024
Est. primary completion date April 22, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 99 Years
Eligibility Inclusion Criteria: - Student enrolled in SMU - Speaks English Exclusion Criteria: - Must have an Apple Watch to use during time of participation in the study

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Relaxation Application
The use of an application for relaxation.
• Relaxation Only
The individual's personal method to relax.

Locations
Country Name City State
United States Southern Methodist University Dallas Texas

Sponsors (1)
Lead Sponsor Collaborator
Sarah Corner

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Sensations Questionnaire Perceived bodily sensations. Scores range from 10-100, where higher scores indicate sensitivity to bodily sensations. at study completion, up to 2 years
Primary Positive and Negative Affect Schedule Immediate experience of mood. The measure consists of two scales, negative and positive items. Scores range from 10-50 for the positive scale, where higher scores indicate greater positive mood, and scores range from 10-50 for the negative scale, where higher scores indicate greater negative mood. at study completion, up to 2 years
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