The Effects of Sleep Disturbances on Fatigue and Cognition in Multiple Sclerosis
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 837
- 试验地点
- 2
- 主要终点
- Severity of Fatigue (cognitive fatigability)
研究概览
简要总结
Fatigue is a prevalent symptom in patients with multiple sclerosis (MS) and is associated with considerable impairment in quality of life as well as loss of occupational capacity. Sleep disturbances are regarded as a critical factor in the development of fatigue and are frequently observed in individuals with MS. However, they often remain underrecognized, undiagnosed, and consequently untreated.
Polysomnography, the gold standard for assessing sleep architecture and quality, has rarely been applied in the investigation of sleep disorders in MS. Accordingly, uncertainties remain regarding the prevalence and extent to which sleep disturbances contribute to fatigue in this population. Moreover, emerging evidence suggests an association between sleep disorders and cognitive dysfunction in MS. Yet, it is unclear whether cognitive impairment arises from the sleep disorder itself, from the resulting fatigue, or from other independent factors.
Pharmacological treatments for MS-related fatigue remain limited, given heterogeneous and frequently non-replicable effects. Non-pharmacological interventions such as physical activity, cognitive behavioral therapy, and psychoeducation have shown promise but yield variable outcomes. The development of novel and effective therapeutic strategies requires a more comprehensive understanding of the etiology of fatigue. To date, the role of sleep disturbances and their relationship to cognitive performance in MS have not been adequately investigated.
The objective of this project is to determine the prevalence and characteristics of sleep disorders in MS patients with fatigue using polysomnography and to examine their relationship with cognitive impairment. In addition, the study will compare sleep quality parameters and the prevalence of sleep disorders across different MS subtypes (relapsing-remitting, primary progressive, and secondary progressive). Furthermore, within a sub-study, it will be investigated whether the type of immunotherapy has an influence on the aforementioned aspects.
Finally, the project seeks to integrate artificial intelligence (AI) into polysomnography analysis to streamline data evaluation and facilitate the future assessment of therapeutic interventions.
The study will be conducted as a non-invasive, non-interventional, longitudinal observational trial including MS patients with fatigue and a control group of patients with subjective sleep complaints but without MS. Recruitment will take place over 36 months at two centers: the Department of Neurology at the University Hospital Düsseldorf and the Maria Hilf Clinics in Mönchengladbach. Additional recruitment will be supported by community-based neurologists in the Mönchengladbach region to broaden the study cohort and ensure representativeness of the study population.
Approximately 382 MS patients are expected to be enrolled. The number of control participants will be determined by the proportion of MS patients presenting with sleep disorders and will be recruited consecutively from the neurological sleep laboratory of the Maria Hilf Clinics. For AI training, retrospective polysomnography data from the past five years (N ≥ 10,000 patients) at the Maria Hilf Clinics will be utilized.
The study protocol includes overnight polysomnography to assess sleep quality, along with comprehensive clinical evaluation, neuropsychological testing, and validated questionnaires addressing fatigue, subjective sleep quality, daytime sleepiness, depression, and anxiety.
Based on manually scored polysomnography, AI models will be trained to identify key parameters of sleep quality. The findings of this study will advance the understanding of the role of sleep disturbances in MS-related fatigue and will facilitate the integration of AI into sleep research, thereby streamlining the evaluation of future therapeutic approaches.
详细描述
- Project Objectives
1.1. In-depth characterization of sleep disorders in MS patients with fatigue.
Exploratory analysis:
Which specific types of sleep disorders are most frequently observed in MS patients with fatigue?
1.2. Comparison of subjective fatigue severity and objectively measured fatigability between patients with and without abnormalities in sleep-related parameters.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Cross Sectional
入排标准
- 年龄范围
- 18 Years 至 79 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Age ≥ 18 and ≤ 79 years (all groups)
- •Adequate (corrected) hearing and vision to complete neuropsychological testing (all groups)
- •Sufficient proficiency in German to participate in assessments (all groups)
- •Capacity to provide informed consent and understanding of study procedures (all groups)
- •Diagnosis of MS according to the 2017 revised McDonald criteria (MS group)
- •Indication for sleep medicine evaluation due to at least mild fatigue, operationalized as ≥ 43 points on the Fatigue Scale for Motor and Cognitive Functions (FSMC) (MS group)
- •Indication for sleep medicine evaluation (control group)
排除标准
- •Lack of signed informed consent or inability to provide consent (all groups)
- •Age < 18 years or > 79 years (all groups)
- •Presence of another neurological disorder in addition to MS, with the exception of migraine (all groups)
- •Use of medications that influence polysomnographic parameters (e.g., benzodiazepines) (all groups)
- •Uncorrected hearing or vision impairment and/or insufficient German language proficiency likely to impact neuropsychological test results (all groups)
研究组 & 干预措施
Multiple Sclerosis
- Diagnosis of MS according to the 2017 revised McDonald criteria
- Indication for sleep medicine evaluation due to at least mild fatigue, operationalized as ≥ 43 points on the Fatigue Scale for Motor and Cognitive Functions (FSMC)
- Age ≥ 18 and ≤ 79 years
- Adequate (corrected) hearing and vision to complete neuropsychological testing
- Sufficient proficiency in German to participate in assessments
- Capacity to provide informed consent and understanding of study procedures
干预措施: No Intervention: Observational Cohort (Other)
Control group
- Indication for sleep medicine evaluation
- Age ≥ 18 and ≤ 79 years
- Adequate (corrected) hearing and vision to complete neuropsychological testing
- Sufficient proficiency in German to participate in assessments
- Capacity to provide informed consent and understanding of study procedures
干预措施: No Intervention: Observational Cohort (Other)
结局指标
主要结局
Severity of Fatigue (cognitive fatigability)
时间窗: Baseline and Follow-up (12-18 Months after Baseline)
Alertness subtest of the Test Battery of Attention (TAP) * Measurement of reaction time * Normalized for age and education * Administered pre- and posttest
Severity of Fatigue (subjective fatigue)
时间窗: Baseline and Follow-up (12-18 Months after Baseline)
Fatigue Scale for Motor and Cognitive Functions (FSMC) * Higher score = Higher fatigue * Min. score: 11 * Max. score: 100
Severity of Fatigue (physical fatigability)
时间窗: Baseline and Follow-up (12-18 Months after Baseline)
Hand-grip-strength dynamometer \- Measurement of grip strength
Sleep disorders according to AASM criteria
时间窗: Baseline and Follow-up (12-18 Months after Baseline)
Diagnostics by medical personnel after 2 nights of polysomnographic measurements.
Verbal Learning and Memory Test (VLMT)
时间窗: Baseline and Follow-up (12-18 Months after Baseline)
Assesses verbal learning, immediate and delayed recall, and recognition of word lists, commonly used to evaluate verbal memory performance.
Symbol Digit Modalities Test (SDMT)
时间窗: Baseline and Follow-up (12-18 Months after Baseline)
Evaluates information processing speed, attention, and visual scanning by requiring rapid symbol-number substitutions.
Brief Visuospatial Memory Test - Revised (BVMT-R)
时间窗: Baseline and Follow-up (12-18 Months after Baseline)
Measures visuospatial learning and memory through repeated recall of geometric figures, including delayed recall and recognition.
次要结局
- Oxygen saturation(Baseline and Follow-up (12-18 Months after Baseline))
- Pittsburgh Sleep Quality Index (PSQI)(Baseline and Follow-up (12-18 Months after Baseline))
- Epworth Sleepiness Scale (ESS)(Baseline and Follow-up (12-18 Months after Baseline))
- Stanford Sleepiness Scale (SSS)(Baseline and Follow-up (12-18 Months after Baseline))
- Insomnia Severity Index (ISI-G)(Baseline and Follow-up (12-18 Months after Baseline))
- International RLS Study Group Rating Scale (IRLS)(Baseline and Follow-up (12-18 Months after Baseline))
- Hospital Anxiety and Depression Scale (HADS)(Baseline and Follow-up (12-18 Months after Baseline))
- Respiratory rate(Baseline and Follow-up (12-18 Months after Baseline))
- Nasal airflow(Baseline and Follow-up (12-18 Months after Baseline))
- Motor fatigability(Baseline & Follow-up (12-18 months after Baseline))
- Cognitive fatigability(Baseline & Follow-up (12-18 months after Baseline))
- Heart rate(Baseline and Follow-up (12-18 Months after Baseline))
- Heart rhythm(Baseline and Follow-up (12-18 Months after Baseline))
- Sleep phase latency(Baseline and Follow-up (12-18 Months after Baseline))
- Total sleep time(Baseline and Follow-up (12-18 Months after Baseline))
- Sleep efficiency(Baseline and Follow-up (12-18 Months after Baseline))
- Arousals(Baseline and Follow-up (12-18 Months after Baseline))
- Apnea-hypopnea Index (AHI)(Baseline and Follow-up (12-18 Months after Baseline))
- Periodic Limb Movement Index (PLMI)(Baseline and Follow-up (12-18 Months after Baseline))
- Electroencephalogram (EEG)(Baseline and Follow-up (12-18 Months after Baseline))
- Electromyogram (EMG)(Baseline and Follow-up (12-18 Months after Baseline))
- Electrooculogram (EOG)(Baseline and Follow-up (12-18 Months after Baseline))
