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Improving Older Adults' Decision Making for OSAT

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03138993
Acronym
eDecide2Rest
Enrollment
36
Registered
2017-05-03
Start date
2017-05-22
Completion date
2018-11-30
Last updated
2019-09-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obstructive Sleep Apnea

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.

Interventions

Web-based patient decision aid plus a paper workbook.

Web-based information about sleep plus a paper workbook

Sponsors

University of California, Los Angeles
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. age \>= 60 years 2. diagnosed with obstructive sleep apnea on a sleep study 3. able to read English-language newspaper text (if needed, using contact lens/glasses) 4. able to write words in a paper booklet 5. scheduled for a sleep clinic appointment with a UCLA sleep provider 6. able to attend a sleep educational session prior to sleep clinic appointment

Exclusion criteria

1. unable to provide informed consent 2. dementia 3. mild cognitive impairment diagnosis or Mini-Cog score \< 3 4. treated for obstructive sleep apnea for \> 30 days prior to scheduled sleep education intervention 5. 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)

Design outcomes

Primary

MeasureTime frameDescription
Recruitment ratesThrough study completion, an average of 1 yearThe investigators will measure recruitment rates for our recruitment strategies
Enrollment ratesThrough study completion, an average of 1 yearThe investigators will measure enrollment rates

Secondary

MeasureTime frameDescription
The length of time for completing the intervention sessionThrough study completion, an average of 1 yearThe investigators will measure the length of time for completing the intervention session

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026