Anxiety Clinical Trial
Official title:
Slow-Breathing Curriculum for Stress Reduction in High School Students: A Feasibility Randomized Controlled Trial
NCT number | NCT05266833 |
Other study ID # | 101 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | January 20, 2021 |
Est. completion date | March 29, 2021 |
Verified date | March 2022 |
Source | Health and Human Performance Foundation |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study was to test a simple slow breathing curriculum for reducing stress among high school students. The curriculum was developed by the Health and Human Performance Foundation and implemented for this study at a public high school in Colorado, United States.
Status | Completed |
Enrollment | 43 |
Est. completion date | March 29, 2021 |
Est. primary completion date | February 2, 2021 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 16 Years to 19 Years |
Eligibility | Inclusion Criteria: Students were eligible to participate in this study if they: 1. Were enrolled at study start (baseline period) in one of four senior (12th grade) English classes taught by the teacher who was recruited for the study; 2. Accepted participation in the study, including willingness to abide by the randomization process, by signing student assent on the consent form; 3. Had parental permission to participate in the study, indicated by their signing their consent on the consent form. Exclusion Criteria: Students were excluded from the study and data collection, but not from class, if they: 1. Chose not to participate; or, 2. Did not receive parental permission. |
Country | Name | City | State |
---|---|---|---|
United States | Aspen High School | Aspen | Colorado |
Lead Sponsor | Collaborator |
---|---|
Health and Human Performance Foundation |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Feasibility - compliance with breathing curriculum | Number of participants completing the breathing practices | 5 weeks | |
Primary | Feasibility - compliance with effectiveness assessments | Number of participants completing the STAI and CO2TT assessments | 7.5 weeks | |
Primary | Feasibility - curriculum ease and tolerability | Ease and tolerability of the breathing curriculum was measured as the average ratings on a scale of 0 to 3 (worst to best) of responses about the curriculum's ease, usefulness, and tolerability. | 1-week followup period | |
Primary | Feasibility - effectiveness assessments ease and tolerability | Ease and tolerability of the preliminary effectiveness assessments was measured as the average ratings on a scale of 0 to 3 (worst to best) of responses about the effectiveness assessments' ease and tolerability. | 1-week followup period | |
Secondary | Change in in-the-moment stress levels from before to after breathing exercises, as measured by the State-Trait Anxiety Inventory, State (STAI-State) Scale, short version. | 6-item STAI-State, short version scale. Responses are scored from 1 to 4. Final scores range from 6 to 24, with higher scores reflecting higher levels of in-the-moment anxiety. | 5 weeks | |
Secondary | Change in general stress levels from before to after the 5-week curriculum, as measured by the State-Trait Anxiety Inventory, Trait (STAI-Trait) Scale. | 20-item STAI-Trait scale. Responses are scored from 1 to 4. Final scores range from 20 to 80, with higher scores reflecting higher levels of general anxiety. | 1.5-week baseline period and 1-week followup period |
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