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Usability of a Breathing-CBT Platform (CBT = Cognitive Behavioural Therapy)

NCT04776122 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2021-03-01

No results posted yet for this study

Summary

The study will examine the usability of a breathing platform in the home environment. It will be a randomized, open-label crossover study of 10 participants who will complete the CBT and breathing components in their home, prior to sleeping. Usability will be measured by scores assigned by participants. Qualitative feedback and compliance information will also be collected.

Conditions

  • Breathing, Mouth

Interventions

DEVICE

Therapy

Device-assisted breathing for relaxation

OTHER

No device

Breathing platform without device

Sponsors & Collaborators

  • ResMed

    lead INDUSTRY

Principal Investigators

  • Jeff Armitstead · ResMed

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-06-01
Primary Completion
2018-06-30
Completion
2018-07-30

Countries

  • Australia

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04776122 on ClinicalTrials.gov