Sleep and Cardiovascular Health in Adolescence
- Conditions
- Insomnia Type; Sleep Disorder
- Interventions
- Other: No pre-sleep arousal manipulationOther: pre-sleep arousal down-regulationOther: pre-sleep arousal up-regulation
- Registration Number
- NCT03727906
- Lead Sponsor
- SRI International
- Brief Summary
Insomnia is a prevalent and under-recognized disorder in adolescence, particularly in girls, with long-term repercussions for mental and physical health. This study assesses manifestation of autonomic hyperarousal and vulnerability to insomnia using a sample of male and female adolescents with and without Diagnostic and Statistical Manual (DSM-5) Insomnia Disorder. Outcomes from this study have the potential to inform prevention and treatment interventions for insomnia that can be implemented at a young age before chronic negative sequelae of this common disorder manifest.
- Detailed Description
Insomnia is highly prevalent in adolescence, particularly in post-pubertal girls and tends to persist over time. Insomnia is considered a hyperarousal disorder, in which abnormally elevated levels of cognitive and physiological activation, particularly evident at bed-time, prevent individuals from falling asleep and having a restorative night's sleep. Hyperarousal is a major pathophysiological mechanism linking insomnia with poor mental and physical health, including cardiovascular (CV) disease. The investigators and others have shown evidence of autonomic nervous system (ANS) dysfunction such as hyperactivation of the sympathetic branch of the ANS - a major etiological factor in CV disease - in young and midlife adults, both before and during sleep. It is unknown if ANS hyperarousal is evident in adolescents with insomnia.
The biological basis for an emerging sex difference in insomnia prevalence in adolescence is unknown. The investigators' pilot data reveal intriguing evidence of sex-differences in basic and stress-dependent ANS modulation during sleep in adolescents with girls showing a greater ANS response to stress. These data suggest the existence of a predisposing and stress-dependent ANS vulnerability in female adolescents, a potential pathway to develop insomnia. This study takes a novel approach to investigating the manifestation of physiological ANS and CV hyperarousal in adolescents with insomnia by experimentally manipulating the pre-sleep arousal state via stress-induced ANS up-regulation and relaxation-driven ANS down-regulation. In addition, the study focuses on sex differences in ANS and CV responses to pre-sleep ANS manipulation, potentially addressing the question of why female sex is a major risk factor for insomnia.
The investigators aim to test 110 male and female high-school students (16-20y) with and without DSM-5 Insomnia Disorder, during a regular in-lab polysomnographic night (baseline) and under experimental pre-sleep stress (psychosocial stressor) and pre-sleep relaxation (Virtual reality ANS bio-feedback) intervention nights, using state-of-the-art, noninvasive, beat-to-beat ANS and CV measures, including blood pressure, to assess nocturnal ANS and CV function in adolescents with insomnia (Aim 1); the impact of pre-sleep ANS arousal levels on nocturnal ANS and CV function, and sleep in adolescents with and without insomnia, considering possible sex differences (Aim 2), and the extent to which nocturnal ANS and CV function mediate the effect of pre-sleep arousal levels on objective and perceived sleep quality (Aim 3).
This study has the potential to elucidate pathophysiological ANS hyperarousal underlying Insomnia Disorder in adolescence, including potential reasons for the vulnerability to insomnia in girls, leading to better recognition and potentially new treatment strategies of this disorder targeted at the state of ANS hyperarousal in the pre-sleep period.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 115
- Must be post-pubertal
- BMI <30 kg/m-2 to reduce the likelihood of obesity-related sleep-disordered breathing
- Current use of drugs known to affect sleep and CV systems (e.g., Antidepressants, stimulants, beta-blockers)
- Serious history of, or current medical conditions that could affect brain function, or study participation, including Diabetes, cancer, neurological diseases (e.g., Seizure disorders) recurrent migraine, cardiovascular diseases (e.g., Hypertension) and traumatic brain injury with loss of consciousness >30 minutes
- Current DSM-5 diagnosis of Neurodevelopmental Disorders (e.g., Attention-Deficit/Hyperactivity Disorder)
- Current DSM-5 diagnosis of Schizophrenia Spectrum and Other Psychotic Disorders, Bipolar and Related Disorders
- Current DSM-5 diagnosis of Depressive and Anxiety Disorders (e.g., Major Depressive Disorder)
- Current DSM-5 diagnosis of Post-Traumatic Stress Disorder
- Current DSM-5 diagnosis of Substance-Related and Addictive Disorders (e.g., Alcohol Use Disorder)
- History of and persistence in severe learning disorder, pervasive developmental disorder, or other condition requiring repeated or persistent specialized education (e.g., Estimated intellectual quotient (IQ) >2 standard deviations below mean)
- Current psychiatric disorders in both control and insomnia groups is exclusionary
- Past history of psychiatric disorders in controls is exclusionary (past history of psychiatric disorders in the insomnia group is not exclusionary)
- Shift work in the previous year and no time-zone travel in the past month
- Evidence of other DSM-5 Sleep-Wake Disorders (e.g., Narcolepsy), Breathing-Related Sleep Disorders (e.g., Obstructive Sleep Apnea Hypopnea, Circadian Rhythm Sleep-Wake Disorders and particularly Delayed Sleep Phase Type), and Parasomnias (e.g., Non-Rapid Eye Movement Sleep Arousal Disorders, Rapid Eye Movement Sleep Behavior Disorder and Restless Legs Syndrome)
- Current pregnancy
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description Non-insomnia Group pre-sleep arousal down-regulation Non-insomnia participants will not meet criteria for current DSM-5 Insomnia Disorder or have a past history of insomnia. Interventions (order is randomly assigned): 1. no pre-sleep arousal manipulation night; 2. pre-sleep arousal down-regulation night 3. pre-sleep arousal up-regulation night. Non-insomnia Group No pre-sleep arousal manipulation Non-insomnia participants will not meet criteria for current DSM-5 Insomnia Disorder or have a past history of insomnia. Interventions (order is randomly assigned): 1. no pre-sleep arousal manipulation night; 2. pre-sleep arousal down-regulation night 3. pre-sleep arousal up-regulation night. Insomnia Group No pre-sleep arousal manipulation Insomnia Group participants will have to meet DSM-5 criteria for current Insomnia Disorder. Interventions (order is randomly assigned): 1. no pre-sleep arousal manipulation night; 2. pre-sleep arousal down-regulation night 3. pre-sleep arousal up-regulation night. Insomnia Group pre-sleep arousal down-regulation Insomnia Group participants will have to meet DSM-5 criteria for current Insomnia Disorder. Interventions (order is randomly assigned): 1. no pre-sleep arousal manipulation night; 2. pre-sleep arousal down-regulation night 3. pre-sleep arousal up-regulation night. Non-insomnia Group pre-sleep arousal up-regulation Non-insomnia participants will not meet criteria for current DSM-5 Insomnia Disorder or have a past history of insomnia. Interventions (order is randomly assigned): 1. no pre-sleep arousal manipulation night; 2. pre-sleep arousal down-regulation night 3. pre-sleep arousal up-regulation night. Insomnia Group pre-sleep arousal up-regulation Insomnia Group participants will have to meet DSM-5 criteria for current Insomnia Disorder. Interventions (order is randomly assigned): 1. no pre-sleep arousal manipulation night; 2. pre-sleep arousal down-regulation night 3. pre-sleep arousal up-regulation night.
- Primary Outcome Measures
Name Time Method Average nocturnal heart rate (HR), as a measure of cardiac contractility Measured during 1 night (each for baseline, pre-sleep stress and pre-sleep relaxation conditions) Heart rate (HR) response to experimental manipulation
Average nocturnal Pre-ejection period (PEP), as a measure of cardiac sympathetic activity Measured during 1 night (each for baseline, pre-sleep stress and pre-sleep relaxation conditions) Pre-ejection period (PEP) response to experimental manipulation
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
SRI International
🇺🇸Menlo Park, California, United States