NCT06378034尚未招募不适用
Effect of Lactium on Sleep Efficiency and Quality in Healthy Volunteers With Persistent Subclinical Insomnia
Ingredia S.A.0 个研究点目标入组 100 人开始时间: 2024年6月10日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 100
- 主要终点
- Sleep efficiency
研究概览
简要总结
The main objective will be to assess the effect of Lactium® on sleep efficiency in volunteers presented with persistent subclinical insomnia.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 25 Years 至 55 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •In good general and mental health according to the investigator judgement: no clinically significant and abnormalities relevant to medical history or clinical examination
- •Having a Body Mass Index (BMI) of 18.5 < BMI < 30 kg/m2
- •Present subclinical insomnia characterized by an Insomnia Severity Index (ISI) score between 8 and 14 during the last month preceding the screening visit
- •Whose insomnia symptoms started at least 3 months before the screening visit
- •Present a medium level of phycological stress characterized by a Perceived Stress Scale (PSS-10) score between 14 and 26
- •Willing / able to maintain their eating habits and physical activity during the study (no planned diet, no change in physical activity ...)
- •Willing / able to participate in the study in accordance with protocol procedures (dated and signed informed consent form)
- •Affiliated to a Health insurance scheme
- •Agree to be registered in the national database of subjects participating in clinical research
- •Have a smartphone compatible with the NursTrial® e-PRO application
排除标准
- •Presenting moderate to severe insomnia defined by an ISI score greater than or equal to 15 in the last month prior to selection
- •Presenting other sleep disorders already diagnosed or suspected during the screening visit: impatience (restless legs), parasomnias, hypersomnias, sleep apnea, iatrogenic insomnia
- •Subject assessed as "definitely" an evening type people by the Horne and Ostberg's circadian typology questionnaire (delayed phase subject)
- •Whose sleep disorders are related to external factors (noise pollution, young children, etc ...)
- •Workers with atypical schedules (night work, staggered working hours, changes in regular working hours, or shift work)
- •Drug Addict
- •Alcohol consumption greater than 2 glasses per day
- •Subject with excessive caffeine consumption exceeding 400 mg per day (coffee ≈ 80 mg per cup; cola soda≈ 25 mg per glass; tea ≈40 mg per cup; energy drinks ≈70 mg per glass)
- •Subject consuming or having consumed any dietary supplement with an effect or a possible effect on sleep, stress, anxiety, or fatigue during the last 3 months prior to screening visit (melatonin, lactium, ginseng, caffeine ...)
- •Subject who has been treated during the 6 months preceding the screening visit or are currently being treated with non-medication therapies (such as psychotherapy, Cognitive Behavioral Therapy [CBT], Eye Movement Desensitization and Reprocessing [EMDR], etc. or repetitive Transcranial Magnetic Stimulation [TMS]) or psychotropic medication prescribed and / or recommended for anxious manifestations, depression, sleep disorders and generally for any neurological or psychological manifestation
- •Subject with psychiatric comorbidity as described in the Diagnostic and Statistical Manual of Mental Disorders V (DSM-V) (depression, post traumatic stress disorder, etc.) or history of psychiatric illness
- •Untreated or not controlled hypertension
- •Untreated or not controlled thyroid diseases (hypo or hyperthyroidism, Graves' disease...)
- •Epileptic subject
- •Asthmatic subject
- •Any other pathology or medical history or symptomatology likely to significantly influence the study criteria (nocturnal pain, nasal congestion, cough at bedtime or nocturnal cough, nocturnal pollakiuria, tinnitus, etc.) according to the investigator
- •Confirmed cow's milk protein allergy
- •Sleeping on a mattress that is not compatible with the sleep quality recording (water and air mattresses) or does not have adequate or necessary domestic equipment for its operation (power socket near the bed, etc.)
- •Likely to sleep outside their home during the study (holidays, regular business trips, etc.)
- •Whose spouse or partner is participating in this study
- •Pregnant woman (negative urine test at screening and initial/randomization visits) or wishing to be pregnant during the study or breastfeeding
- •Hormonal state that may induce fluctuation in emotional state and sleep during the study, such as, the postpartum period (< 6 months after delivery) and perimenopause (irregular menstrual cycle, hot flashes)
- •Under legal protection (guardianship, curatorship) or deprived of rights following an administrative or judicial decision
- •Psychologically or linguistically incapable of understanding and signing informed consent
- •Participating in another clinical trial or in exclusion period of a previous clinical trial
- •Having reached the maximum research compensation threshold stipulated by regulations.
结局指标
主要结局
Sleep efficiency
时间窗: Before treatment (day 0); at the end of the treatment (after 29 days)
The primary endpoint will be changes between baseline and final sleep efficiency (SE), measured nightly using actigraphy
次要结局
- Sleep diary(Before treatment (day 0); at the end of the treatment (after 29 days))
- Insomnia Severity Index(Before treatment (day 0); at the end of the treatment (after 29 days))
- PSQI(Before treatment (day 0); at the end of the treatment (after 29 days))
- Sleep quality by cctigraphy(Before treatment (day 0); at the end of the treatment (after 29 days))
研究者
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