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Mechanisms Underlying the Blood Pressure Lowering Effect of Sleep

Beth Israel Lahey Health logo

Beth Israel Lahey Health

Status

Completed

Conditions

Hypertension

Treatments

Behavioral: Sleep Timing
Behavioral: Sleep Extension

Study type

Interventional

Funder types

Other

Identifiers

NCT03043963
2015P000243

Details and patient eligibility

About

The main purpose of this study is to learn about the influence of two different behavioral interventions (lasting 8 weeks) involving sleep for lowering blood pressure, and to study the mechanisms involved. There is research evidence that healthy sleep promotes heart-health and may decrease blood pressure, and that sensitivity to insufficient or disrupted sleep may be influenced by sex. This research will compare two interventions that are each designed to improve sleep health, and will investigate sex differences in response. The project includes 3 in-hospital stays with biological measurements to evaluate the underlying mechanisms associated with the effectiveness of two different blood pressure lowering behavioral interventions.

Full description

The study involves home-based sleep-wake data collection before and during behavioral intervention, and 3 overnight stays in the hospital. For each hospital stay participants will be asked to arrive in the afternoon, and stay until the next evening. They will be provided dinner on the first day and breakfast, lunch and dinner on the second day. If they are taking any blood pressure medication they will continue to take it through the study. During the in-hospital stays, blood pressure will be measured continuously using two small finger cuffs. In order to monitor and record brain waves to determine sleep and wakefulness, small gold-coated disks called electrodes will be placed on the head and body. Heart rate, blood pressure and brain activity will be recorded for a little over 24 hours on each in-hospital stay. Before as well as during the in-hospital stays questions will be asked about sleep times, subjective sleepiness and other indices relating to well-being.

Enrollment

270 patients

Sex

All

Ages

25 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • pre-hypertension or stage one hypertension (BP ≥120/80 and <160/100).
  • usual sleep period occurs at night

Exclusion criteria

  • significant active or uncontrolled sleep disorders
  • shiftwork
  • current pregnancy
  • diabetic patients who are insulin dependent (or have HbA1c>9.0%)
  • current use of hypnotics or clonidine
  • renal/electrolyte disorders and any other condition that the study screening physician considers would significantly impede participation in the study

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

270 participants in 2 patient groups

Sleep Timing
Active Comparator group
Description:
Intervention will include basic education concerning sleep hygiene and regularity of sleep timing
Treatment:
Behavioral: Sleep Timing
Sleep Extension
Experimental group
Description:
Intervention will include basic education concerning sleep hygiene and an extension of the sleep period.
Treatment:
Behavioral: Sleep Extension

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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