Motivational Enhancement - Acute Decompensated Heart Failure and OSA
Primary Purpose
Acute Decompensated Heart Failure, Obstructive Sleep Apnea, Motivational Enhancement
Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Telemedicine Intensive Motivational Enhancement
Sponsored by
About this trial
This is an interventional other trial for Acute Decompensated Heart Failure
Eligibility Criteria
Inclusion Criteria:
- Admitting ADHF diagnosis
- OSA diagnosis (REI ≥5)
- Treatment-naive and agreeable to PAP therapy
- Agrees to participate.
Exclusion Criteria:
- Prior or current PAP therapy
- Unable to provide informed consent
- Moderately hypoxic (oxygen saturation < 87% on room air or requiring >2L of O2 during overnight sleep study
- Hemodynamically unstable (systolic blood pressure, SBP<90 mmHg, heart rate>120bpm)
- Central predominant apnea (Central Apnea Index > 50% of the Apnea Index) Dementia/cognitive dysfunction
- Unable to participant in video televisits.
Sites / Locations
- Cleveland Clinic FoundationRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Experimental
Arm Label
Standard of Care with provider
Telemedicine Intensive Motivational Enhancement
Arm Description
Participant will continue follow up for sleep apnea with provider.
Participants will attend a telemedicine motivational enhancement visit to improve PAP adherence along with regular follow up for sleep apnea
Outcomes
Primary Outcome Measures
PAP Adherence (TIME versus Standard of Care)
average hourly use per night
PAP Adherence (TIME versus Standard of Care)
average hourly use per night
Functional Outcomes of Sleep Questionnaire (TIME versus Standard of Care)
Functional Outcomes of Sleep Questionnaire (FOSQ-10): Subscale scores range from 1-4 (1= extreme difficulty, 2= moderate difficulty, 3= a little difficulty, 4= no difficulty) with total scores ranging from 5-20 with higher scores indicating better functional status.
Kansas City Cardiomyopathy Questionnaire (TIME versus Standard of Care)
Kansas City Cardiomyopathy Questionnaire (KCCQ-12):: physical limitation, symptom frequency, quality of life, and social limitation. Scores ranges from 5-30, higher KCCQ-12 scores from baseline represent better health status
Secondary Outcome Measures
Full Information
NCT ID
NCT04752462
First Posted
February 9, 2021
Last Updated
July 7, 2023
Sponsor
The Cleveland Clinic
Collaborators
American Academy of Sleep Medicine
1. Study Identification
Unique Protocol Identification Number
NCT04752462
Brief Title
Motivational Enhancement - Acute Decompensated Heart Failure and OSA
Official Title
Effect of Post-Discharge Telemedicine Motivational Enhancement Intervention in Heart Failure and Obstructive Sleep Apnea on Adherence and Health Outcomes
Study Type
Interventional
2. Study Status
Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 13, 2021 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Cleveland Clinic
Collaborators
American Academy of Sleep Medicine
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
A feasibility randomized controlled trial will be conducted with a 6-month follow up to: Examine the impact of early intensive telemedicine motivational enhancement (TIME) vs standard of care on PAP adherence (n=40/group) and continuity of care at 3 and 6 months post-discharge in patients admitted with ADHF with a new inpatient diagnosis of OSA(REI>5). Assess the effect of early telemedicine integrated with motivational enhancement (TIME) vs standard of care on patient reported outcomes including Functional Outcomes of Sleep questionnaire (FOSQ-10), Kansas City Cardiomyopathy Questionnaire (KCCQ-12). Investigate the impact of early TIME vs standard of care on 6-month hospital readmissions.
Detailed Description
As part of our inpatient sleep testing program, high-risk HF patients undergo Type III sleep testing (Nihon Kohden®) set up by sleep laboratory technicians. Our inpatient sleep service also has a clinical nurse who works with patients on CPAP education, set up and assists with post hospital sleep care. If a titration study is needed, it is generally arranged 1-2 weeks post discharge. All inpatient sleep studies are scored by three registered polysomnographic technologists and I review and finalize these studies (current clinical flow as the primary physician leading the inpatient service, which will be augmented for this clinical trial). A research coordinator and I will approach those with REI>5 who meet eligibility per screening in Epic®, to discuss sleep study results, confirm eligibility, invite the patient to participate, and if interested, will obtain written informed consent. Consent: Consent form will explain in a lay person' terminology the nature of all procedures. It will be stressed that participation is voluntary. The research coordinator and the PI will be available to answer questions. All activities will be compliant with local IRB and HIPPA guidelines.
All participants will obtain Auto-CPAP from two manufacturers (Philips Respironics ® or ResMed ®) delivered by the same homecare health before discharge. PAP pressures will be set at 5-15 cmH2O, heated humification, and expiratory pressure relief according to comfort. A modem will be attached to the PAP device to extract adherence data remotely (SD card for those without wireless capability). All patients will receive a standardized 20-minute educational session about PAP therapy before discharge and will be advised to use their device every night during sleep by our clinical nurse. Patients will also be fitted for a mask fitted homecare health. If participants have mask or pressure intolerance issues, they will be a direct provided a phone number to our research coordinator. All baseline questionnaires will be sent via REDcap link to the patient's e-mail or completed in paper form before discharge and during their visit (or paper if electronic not feasible). The coordinator will ensure all questionnaires are completed before discharge and will instruct patients to complete follow-up questionnaires. Patients will be randomized (REDCap algorithm) 1:1 to TIME versus standard of care. Blocks will be of random size blinded to study investigators. Although it will not be feasible to blind the research team and participants to the intervention, the standard of care group will also receive sleep hygiene education so that there is perception of some level of intervention to try to address placebo effect. During follow up visits (2 weeks and 2 months for the TIME group and 2 months standard of care group) with sleep medicine, the first 15 minutes will be focused on OSA and troubleshooting problems for both groups as this is standard clinical care provided at our Sleep Disorders Center. These 15 minutes will be followed by 30 minutes of ME in the intervention group and 10 minutes of sleep hygiene education in the control group. Outcomes will be measured at 3 months and 6 months for both groups. Both groups will receive a booster phone call at 4 months. The intervention group will receive a 30 minutes booster ME session and the control group will receive 10 minutes of sleep hygiene.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Decompensated Heart Failure, Obstructive Sleep Apnea, Motivational Enhancement, PAP Adherence
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
80 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Standard of Care with provider
Arm Type
No Intervention
Arm Description
Participant will continue follow up for sleep apnea with provider.
Arm Title
Telemedicine Intensive Motivational Enhancement
Arm Type
Experimental
Arm Description
Participants will attend a telemedicine motivational enhancement visit to improve PAP adherence along with regular follow up for sleep apnea
Intervention Type
Behavioral
Intervention Name(s)
Telemedicine Intensive Motivational Enhancement
Other Intervention Name(s)
TIME
Intervention Description
Participants will attend a telemedicine motivational enhancement visit to improve PAP adherence along with regular follow up for sleep apnea
Primary Outcome Measure Information:
Title
PAP Adherence (TIME versus Standard of Care)
Description
average hourly use per night
Time Frame
3 Month
Title
PAP Adherence (TIME versus Standard of Care)
Description
average hourly use per night
Time Frame
6 Month
Title
Functional Outcomes of Sleep Questionnaire (TIME versus Standard of Care)
Description
Functional Outcomes of Sleep Questionnaire (FOSQ-10): Subscale scores range from 1-4 (1= extreme difficulty, 2= moderate difficulty, 3= a little difficulty, 4= no difficulty) with total scores ranging from 5-20 with higher scores indicating better functional status.
Time Frame
2 Months
Title
Kansas City Cardiomyopathy Questionnaire (TIME versus Standard of Care)
Description
Kansas City Cardiomyopathy Questionnaire (KCCQ-12):: physical limitation, symptom frequency, quality of life, and social limitation. Scores ranges from 5-30, higher KCCQ-12 scores from baseline represent better health status
Time Frame
2 Months
Other Pre-specified Outcome Measures:
Title
Impact of TIME vs Standard of Care on 6-month hospital readmissions
Description
6-month hospital readmissions
Time Frame
6 Month
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Admitting ADHF diagnosis
OSA diagnosis (REI ≥5)
Treatment-naive and agreeable to PAP therapy
Agrees to participate.
Exclusion Criteria:
Prior or current PAP therapy
Unable to provide informed consent
Moderately hypoxic (oxygen saturation < 87% on room air or requiring >2L of O2 during overnight sleep study
Hemodynamically unstable (systolic blood pressure, SBP<90 mmHg, heart rate>120bpm)
Central predominant apnea (Central Apnea Index > 50% of the Apnea Index) Dementia/cognitive dysfunction
Unable to participant in video televisits.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Joan Aylor, BA
Phone
216-445-1698
Email
aylorj@ccf.org
First Name & Middle Initial & Last Name or Official Title & Degree
Cinthya Pena Orbea, MD
Phone
216-445-1356
Email
penac@ccf.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Cinthya Pena Orbea, MD
Organizational Affiliation
The Cleveland Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cleveland Clinic Foundation
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44195
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Joan Aylor, BA
Phone
216-445-1698
Email
aylorj@ccf.org
First Name & Middle Initial & Last Name & Degree
Cinthya Pena Orbea, MD
Phone
216-445-1365
Email
penac@ccf.org
12. IPD Sharing Statement
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Motivational Enhancement - Acute Decompensated Heart Failure and OSA
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