A Randomized, Double-Blind, Placebo Controlled, Single Center Pilot Study to Assess the Impact of Sleep Supplement on Sleep Health
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- Pharmanex
- 入组人数
- 40
- 主要终点
- Change from baseline sleep quality index
研究概览
简要总结
Sleep is essential for health and wellness. Sleep disruption can occur due to emotional stress, advancing age, hormonal imbalance, medications, and many other causes, some of which are presently unknown. Most pharmaceutical sleep products artificially induce sedation without providing quality sleep. Thus, a need exists for safe dietary supplement to promote and support healthy sleep that will encourage restful sleep. This study will examine the efficacy, tolerance, and safety of sleep supplement as compared to a placebo.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Triple (Participant, Investigator, Outcomes Assessor)
盲法说明
Products will be delivered in forms that it will not be discernable (to participant, investigator, or care provider) as to which product is active or placebo
入排标准
- 年龄范围
- 20 Years 至 60 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •The subject is male or female 20-60 years of age at the time of informed consent.
- •Recorded baseline BMI is ≥18.5 and ≤29.9 kg/m
- •A score of 5 or higher on the Pittsburgh Sleep Quality Index.
- •Willing and able to give informed consent
- •Willing to maintain consistent diet and physical activity through the study period.
- •Willing to limit alcohol consumption to ≤14 drinks per week, no more than 4 drinks at a time, and no more than 1 drink within 4h of bedtime.
- •Willing to limit caffeine consumption to no more than 4 servings per day and no caffeine within 6h of bedtime.
排除标准
- •Could not or did not want to participate in clinical study.
- •Taken nutritional supplements for sleep or stress in the previous 6 months.
- •Have received non-pharmacological treatment for sleep disorders (eg. Cognitive behavioral therapy, relation therapy) in previous 6 months
- •Any known allergy or intolerance to any of the ingredients contained in supplement.
- •Planned surgical procedure during the course of the study.
- •Used nicotine in the past 6 months.
- •Have a major psychiatric disorder as determined by the Mini International Neuropsychiatric Inventory
- •A history of unconventional sleep pattern, a diagnosed sleep disorder, or chronic medical condition that could affect energy/fatigue levels.
- •Consume more than 400mg of caffeine per day in the past 2 weeks.
- •Used any psychotropic medications, stimulants, cannabis, non-registered drug products, or illicit substances in the past 4 weeks.
- •At risk of drug or alcohol abuse
- •Used any sleep aids in the past 2 weeks.
- •Employed in night shift work or rotational shift work
- •Currently pregnant, nursing, planning to become pregnant, or unwilling to use a medically approved form of contraception will be excluded.
- •Individuals who sleep more than 10 hours.
- •Typically take a nap during the day.
- •Those planning travel or vacation during the study period.
结局指标
主要结局
Change from baseline sleep quality index
时间窗: Baseline, Day 1, Day 7, Day 28
Change from baseline in validated Pittsburgh Sleep Quality Index (0-21, higher number indicates poorer quality)
Change from baseline sleep duration and quality from diary
时间窗: Baseline and Daily for 28 days
Change from baseline with Daily Sleep Diary
次要结局
- Change from baseline perceived stress scale(Baseline, Day 1, Day 7, Day 28)
- Change from baseline in mood(Baseline, Day 1, Day 7, Day 28)
- Change from baseline Insomnia severity index(Baseline, Day 1, Day 7, Day 28)
- Change from baseline in skin attributes(Baseline, Day 7, and Day 28)
- Change from baseline in restorative sleep as measured by Restorative Sleep Questionnaire (RSQ)(Baseline, Day 1, Day 7, Day 28)