IRCT20240217061029N1尚未招募3 期
Investigating the Effectiveness of the Traditional Persian Medicine Product based on the Apium Graveolens on the Sleep Quality and Quality of Life of the Community-Dwelling Elderly
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 入组人数
- 70
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 60 years 至 no limit（—）
- 性别
- All
入选标准
- •Desire to Participate in the Study and Give Informed Consent
- •Age 60 Years and Older
- •Low Quality of Sleep based on the Pittsburgh Sleep Quality Standard Questionnaire (Score 5 and above)
- •Not Having Cognitive Impairment and Speech Impairment (Getting a Score of 25 or Higher on the MMSE Test)
- •Not Having Diagnosed Mental Disorders that Interfere with Sleep, such as Restless Leg Syndrome, Obstructive Sleep Apnea, and Severe Depression and Anxiety Disorders, and are Treated with Relevant Drugs
- •Not Having Dependence on any Narcotic Drugs, Sleeping Pills and Alcohol and Not Consuming These Items in the Last Month
- •Not Having any History of Allergy to Celery and Similar Compounds
- •Not Taking Drugs that Affect the Sleep-Wake Cycle and Anticoagulants
- •Not Suffering from Physical Diseases that Affect the Sleep-Wake Cycle, such as Cancer, Liver and Kidney Disorders, Severe Anemia that Requires Treatment, and Coronary Heart Disorders.
- •Not having Epilepsy, History of low Blood Pressure
- •The Ability to Consume the Product Orally
排除标准
- •Not Taking Medicine for 5 Consecutive Nights or 10 Alternating Nights
- •Showing any Allergic Reaction to the Drug
- •Reluctance to Cooperate
- •Leaving the Study due to Reasons such as Death and Illness
- •Unfortunate Events such as the Death of Relatives
研究者
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