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Clinical Trials/NCT03138993
NCT03138993
Completed
N/A

Improving Older Adults' Decision Making for Obstructive Sleep Apnea Treatment (Phase 3)

University of California, Los Angeles1 site in 1 country36 target enrollmentMay 22, 2017

Overview

Phase
N/A
Intervention
Not specified
Conditions
Obstructive Sleep Apnea
Sponsor
University of California, Los Angeles
Enrollment
36
Locations
1
Primary Endpoint
Recruitment rates
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

This study evaluates the feasibility of conducting a randomized controlled trial that tests a patient decision aid for obstructive sleep apnea in older adults with newly-diagnosed obstructive sleep apnea treated in an outpatient sleep clinic. Half of the participants will use a patient decision aid, while the other half will receive general information about sleep.

Detailed Description

Patient decision aids are one strategy for helping older adults make informed decisions about treatments. Patient decision aids improve patients' knowledge about therapies and encourage them to actively weigh the risks and benefits of each therapy.

Registry
clinicaltrials.gov
Start Date
May 22, 2017
End Date
November 30, 2018
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Constance Fung, MD, MSHS

Principal Investigator

University of California, Los Angeles

Eligibility Criteria

Inclusion Criteria

  • age \>= 60 years
  • diagnosed with obstructive sleep apnea on a sleep study
  • able to read English-language newspaper text (if needed, using contact lens/glasses)
  • able to write words in a paper booklet
  • scheduled for a sleep clinic appointment with a UCLA sleep provider
  • able to attend a sleep educational session prior to sleep clinic appointment

Exclusion Criteria

  • unable to provide informed consent
  • mild cognitive impairment diagnosis or Mini-Cog score \< 3
  • treated for obstructive sleep apnea for \> 30 days prior to scheduled sleep education intervention
  • severe physical or mental illness (e.g., hospitalized within past 7 days prior to scheduled sleep education intervention, substance abuse within 90 days of sleep education intervention)

Outcomes

Primary Outcomes

Recruitment rates

Time Frame: Through study completion, an average of 1 year

The investigators will measure recruitment rates for our recruitment strategies

Enrollment rates

Time Frame: Through study completion, an average of 1 year

The investigators will measure enrollment rates

Secondary Outcomes

  • The length of time for completing the intervention session(Through study completion, an average of 1 year)

Study Sites (1)

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