رادار التجارب AI | ||
|---|---|---|
حالة التجربة السريرية NCT07495423 لـ Sleep Disorder (Disorder)، اضطرابات المزاج هي نشط (لا يقبل مشاركين جدد). اطلعوا على جميع التفاصيل في عرض البطاقة الخاص برادار التجارب السريرية وأدوات اكتشاف الذكاء الاصطناعي. أو يمكنكم طرح أي سؤال هنا. | ||
تجربة واحدة تطابق معايير الفلتر
عرض البطاقة
Exploring the Efficacy of a Breathing Training Intervention in Patients With Emotionally Regulated Sleep Disorders ١٨٨
تفاصيل التجربة السريرية متاحة بشكل أساسي باللغة الإنجليزية. ومع ذلك، يمكن لـ رادار التجارب AI مساعدتك؛ ما عليك سوى النقر على «وصف الدراسة» لعرض ومناقشة معلومات التجربة باللغة التي اخترتها.
التجربة السريرية NCT07495423 هي دراسة تدخُّلية لـSleep Disorder (Disorder)، اضطرابات المزاج وهي نشط (لا يقبل مشاركين جدد). بدأت في ٥ محرم ١٤٤٦ هـ مع خطة لتجنيد ١٨٨ مشاركًا. يقودها Qilu Hospital of Shandong University، ومن المتوقع اكتمالها بحلول ٢٦ ذو الحجة ١٤٤٨ هـ. تم تحديث البيانات الأخيرة من ClinicalTrials.gov في ٨ شوال ١٤٤٧ هـ.
الملخص
In recent years, the incidence of sleep disorders, especially insomnia, has been rising. Insomnia can directly lead to damage to patients' daytime functions, such as daytime sleepiness, inattention, etc., affecting people's normal work and life. Insomnia is related to dysfunction of multiple systems such as the cardiovascular and cerebrovascular systems, endocrine systems, digestion and breathing, and plays a vital r...عرض المزيد
العنوان الرسمي
Exploring the Efficacy of a Breathing Training Intervention in Patients With Emotionally Regulated Sleep Disorders
الحالات الطبية
Sleep Disorder (Disorder)اضطرابات المزاجالمنشورات
مقالات علمية وأوراق بحثية منشورة حول هذه التجربة السريرية:معرّفات دراسة أخرى
- 293688
NCT معرّف
تاريخ البدء (فعلي)
2024-07-11
آخر تحديث مُنشور
2026-03-27
تاريخ الاكتمال (المقدر)
2027-06-01
عدد المشاركين المخطط لهم
١٨٨
نوع الدراسة
تدخُّلية
المرحلة
غ/م
الحالة
نشط (لا يقبل مشاركين جدد)
الكلمات الرئيسية
Insomnia
Breathing exercises
heart rate variability
mood disorder
autonomic nervous system
Breathing exercises
heart rate variability
mood disorder
autonomic nervous system
الغرض الأساسي
العلاج
طريقة توزيع المشاركين
غ/م
نموذج التدخل
المجموعة الواحدة
التعمية
لا شيء (تجربة مفتوحة)
مجموعات/التدخلات
| مجموعة المشاركين/الذراع | التدخل/العلاج |
|---|---|
تجريبيةconventional clinical intervention Health education and publicity for patients and their families, informing them of medication precautions, dietary guidance | respiratory training intervention The study group received a two-week breathing training program in addition to routine clinical care. The program consisted of three exercises rotated daily: pursed-lip breathing involving slow exhalation through pursed lips at a 2:1 exhalation-to-inhalation ratio, practiced for 15 minutes three times daily; balloon blowing requiring patients to slowly inflate five 1000ml balloons within 15 minutes; and breathing trai...عرض المزيد |
النتيجة الرئيسية
النتيجة الثانوية
| مقياس النتيجة | وصف القياس | الإطار الزمني |
|---|---|---|
Sleep Onset Latency | Time from lights-off to objectively defined sleep onset determined by sleep staging using the SOMNOmedics HST device, reported in minutes. | After 2 weeks, 1 month, 2 months, and 3 months |
Wake After Sleep Onset | Total duration of wakefulness occurring after sleep onset during the night, reported in minutes. | After 2 weeks, 1 month, 2 months, and 3 months |
Sleep Efficiency | Percentage of total sleep time relative to total time in bed during overnight monitoring, reported as a percentage (%). | After 2 weeks, 1 month, 2 months, and 3 months |
Total Sleep Time | Total duration of sleep recorded during overnight monitoring using the SOMNOmedics HST device, reported in minutes. | After 2 weeks, 1 month, 2 months, and 3 months |
| مقياس النتيجة | وصف القياس | الإطار الزمني |
|---|---|---|
Low-Frequency Power of Heart Rate Variability | Low-frequency power component of heart rate variability measured using 24-hour ambulatory electrocardiography, reflecting combined sympathetic and parasympathetic activity, reported in milliseconds squared (ms²). | After 2 weeks, 1 month, 2 months, and 3 months |
High-Frequency Power of Heart Rate Variability | High-frequency power component of heart rate variability measured using 24-hour ambulatory electrocardiography, primarily reflecting parasympathetic (vagal) activity, reported in milliseconds squared (ms²). | After 2 weeks, 1 month, 2 months, and 3 months |
Standard Deviation of Normal-to-Normal Intervals | Standard deviation of normal-to-normal (NN) R-R intervals derived from 24-hour ambulatory electrocardiography as a time-domain measure of overall heart rate variability, reported in milliseconds (ms). | After 2 weeks, 1 month, 2 months, and 3 months |
Pittsburgh Sleep Quality Index (PSQI) | Pittsburgh Sleep Quality Index (PSQI) assesses sleep quality, latency, efficiency, disturbances, medication use, and daytime dysfunction with a total score ranging from 0 to 21, where higher scores indicate poorer sleep quality. | after 2 weeks, after 1 month, after 2 months, after 3 months |
The Insomnia Severity Index | The Insomnia Severity Index (ISI) evaluates the severity of insomnia, distress, and impact on daytime functioning, scoring from 0 to 28, with higher scores indicating more severe insomnia. | after 2 weeks, after 1 month, after 2 months, after 3 months |
The Montreal Cognitive Assessment | The Montreal Cognitive Assessment (MoCA) covers attention, executive functions, memory, language, visuospatial abilities, abstraction, calculation, and orientation, with a total score from 0 to 30, lower scores suggesting worse cognitive function. | after 2 weeks, after 1 month, after 2 months, after 3 months |
The Mini-Mental State Examination (MMSE) | The Mini-Mental State Examination (MMSE) assesses orientation, memory, attention, calculation, recall, and language, with a total score from 0 to 30, lower scores indicating worse cognitive function. | after 2 weeks, after 1 month, after 2 months, after 3 months |
The Hamilton Anxiety Scale | The Hamilton Anxiety Scale (HAMA) measures anxiety's somatic and psychological symptoms, scoring from 0 to 56, with higher scores indicating more severe anxiety symptoms. | after 2 weeks, after 1 month, after 2 months, after 3 months |
The Hamilton Depression Rating Scale | The Hamilton Depression Rating Scale (HAMD) evaluates depressive symptoms across mood, cognition, physical, and behavioral aspects, with a total score from 0 to 52, higher scores indicating more severe depressive symptoms. | after 2 weeks, after 1 month, after 2 months, after 3 months |
The Epworth Sleepiness Scale | The Epworth Sleepiness Scale (ESS) assesses daytime sleepiness, scoring from 0 to 24, with higher scores indicating more severe sleepiness. | after 2 weeks, after 1 month, after 2 months, after 3 months |
مساعد المشاركة
معايير الأهلية
الأعمار المؤهلة للدراسة
بالغ, كبار السن
العمر الأدنى للدراسة
18 Years
الجنس المؤهل
الكل
يقبل المتطوعين الأصحاء
نعم
- Meet the diagnostic criteria for insomnia disorder.
- Be between 18 and 80 years of age, inclusive.
- Have questionnaire scores indicating clinical significance:
Pittsburgh Sleep Quality Index (PSQI) score > 5 Insomnia Severity Index (ISI) score > 7 Hamilton Anxiety Scale (HAMA) score > 7 and/or Hamilton Depression Scale (HAMD) score ≥ 7
- Be able to communicate effectively and provide informed consent in the primary language of the study site.
- Provide written informed consent prior to participation
- Insomnia that is secondary to another underlying physical or medical condition.
- A primary diagnosis of another sleep disorder (e.g., sleep apnea, restless legs syndrome) or a primary mood disorder that is considered the main cause of sleep disturbance.
- Chronic sleep disturbances primarily attributable to environmental or lifestyle factors (e.g., shift work, excessive noise, childcare duties).
Qilu Hospital of Shandong Universityلا توجد بيانات اتصال.
1 مواقع الدراسة في 1 بلدان
Shandong
Qilu Hospital of Shandong University, Jinan, Shandong, 266700, China