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Behavioral Intervention
Cognitive Behavioral Therapy for Insomnia in High Blood Pressure
N/A
Waitlist Available
Led By Andrew Sherwood, PhD
Research Sponsored by Duke University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
A current diagnosis of insomnia disorder as defined in the International Classification of Sleep Disorders (ICSD-3); or undiagnosed, but suspected, insomnia disorder that is confirmed at their screening lab visit
Be between 18 and 65 years old
Must not have
Congestive heart failure
Diabetes
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, 6 week, 12 week, 6 months post intervention
Awards & highlights
No Placebo-Only Group
Summary
This trial looks at the connection between high blood pressure, insomnia, and heart disease.
Who is the study for?
This trial is for adults with high blood pressure (systolic BP ≥ 130 mm Hg) and insomnia, either diagnosed or suspected. It's not for those who've had recent heart issues, severe heart conditions, are pregnant, have severe obesity (BMI>40), uncontrolled hypertension (>160/100 mm Hg), certain mental health disorders, substance abuse history within the last year, or other specific medical exclusions.
What is being tested?
The study tests if Cognitive Behavioral Therapy for Insomnia (CBT-I) can reduce cardiovascular risks in patients with both hypertension and insomnia. The goal is to understand how treating insomnia affects heart health in these individuals.
What are the potential side effects?
CBT-I generally has minimal side effects compared to medication; however, some may experience temporary increases in anxiety or stress during therapy as they change their sleep habits and confront beliefs about sleep.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I have been diagnosed with insomnia or suspect I have it.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have been diagnosed with congestive heart failure.
Select...
I have diabetes.
Select...
I have severe hearing or speech impairments.
Select...
I have been diagnosed with moderate or severe sleep apnea.
Select...
I have atrial fibrillation.
Select...
I have a sleep disorder that needs treatment beyond this study.
Select...
I have been diagnosed with psychosis or bipolar disorder.
Select...
I have a known cause for my high blood pressure.
Select...
I have serious heart valve problems that haven't been treated.
Select...
My BMI is over 40.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline, 6 week, 12 week, 6 months post intervention
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, 6 week, 12 week, 6 months post intervention
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change in blood pressure during the nighttime sleep period
Change in sleep during the nighttime sleep period
Changes in insomnia severity
Secondary study objectives
Change in Office Blood Pressure
Change in arterial stiffness
Change in awake blood pressure
+8 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Cognitive Behavioral Therapy for InsomniaExperimental Treatment1 Intervention
Cognitive Behavioral Therapy for Insomnia (CBT-I) 6 sessions of Cognitive Behavioral Training for Insomnia (1 hour each).
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Cognitive Behavioral Therapy for Insomnia (CBT-I)
2014
N/A
~720
Find a Location
Who is running the clinical trial?
National Institutes of Health (NIH)NIH
2,810 Previous Clinical Trials
8,159,482 Total Patients Enrolled
Duke UniversityLead Sponsor
2,451 Previous Clinical Trials
3,066,920 Total Patients Enrolled
Andrew Sherwood, PhDPrincipal InvestigatorDuke University
4 Previous Clinical Trials
666 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- Your blood pressure is not well controlled and is higher than 160/100 mm Hg when measured at the doctor's office.People who work different shifts at different times of the day.I have been diagnosed with congestive heart failure.I am receiving or have received PTSD treatment focused on facing my fears.I have diabetes.You have had problems with drinking alcohol or using drugs in the past year.I am taking medication for my heart condition.I have not had a heart attack or any heart surgery in the last 6 months.I have severe hearing or speech impairments.You have dementia.I have been diagnosed with moderate or severe sleep apnea.You have strong thoughts about hurting yourself or others, as determined through a talk with a doctor.I have atrial fibrillation.You have a pacemaker.Your blood pressure is consistently higher than 130 mm Hg when measured twice.You are currently taking part in another study to help with insomnia.I am taking medication for high blood pressure.I have a sleep disorder that needs treatment beyond this study.My insomnia is mainly due to a medical or psychiatric condition.I have been diagnosed with psychosis or bipolar disorder.I have a known cause for my high blood pressure.I have been diagnosed with insomnia or suspect I have it.You have been in a psychiatric hospital in the last year.I have serious heart valve problems that haven't been treated.My BMI is over 40.
Research Study Groups:
This trial has the following groups:- Group 1: Cognitive Behavioral Therapy for Insomnia
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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