Medical Faculty, Heinrich-Heine-University
Düsseldorf, North Rhine-Westphalia, 40225, Germany
Location status: Recruiting
NCT Number: NCT06937723
This observational study seeks to investigate the underlying of spasticity in patients with multiple sclerosis (MS) by employing multimodal monitoring techniques. By integrating digital biomarkers alongside clinical monitoring, the investigators aim to evaluate whether digital measurements are suitable for monitoring spasticity-related everyday limitations and to compare them with established clinical scores, blood analyses and questionnaires including sores on quality of life, sleep quality or activities of daily living.
Interested in participating?
Request Info18 year and older
All sexes
Observational
Düsseldorf, North Rhine-Westphalia, 40225, Germany
Location status: Recruiting
The symptomatic treatment of spasticity in patients with multiple sclerosis (MS) is a major challenge for both patients and healthcare providers. However, monitoring and measuring the success or failure of treatments in clinical practice remains difficult. This is mainly due to the lack of clinical scores and biomarkers that can be easily and longitudinally collected. Existing scores (such as questionnaires and the Modified Ashworth scale) are rarely used in practice. In addition, the monitoring of side effects (such as dizziness, nausea and fatigue) is difficult in routine clinical practice and often leads to premature discontinuation or switching of treatment. As a result, therapeutic options are often exhausted prematurely. Continuous monitoring with sensitive assessments could enable a better understanding of spasticity treatment.
Approximately 50 patients with moderate and severe spasticity due to MS are to be included in the study. After inclusion, follow-up examinations are carried out every 12 weeks; a total of 3 visits are planned, including the baseline examination.
The study aims to improve the understanding of spasticity symptoms and assess them in patients through multimodal clinical and longitudinal digital measurements.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Patients must meet all the following criteria to be eligible to participate in the study:
Exclusion criteria
All-day monitoring of patients via smartwatch
Time frame: 180 days
Time frame: 180 days
Time frame: 180 days
Time frame: 180 days
Time frame: 180 days
Time frame: 180 days
Time frame: 180 days
Time frame: 180 days
Time frame: 180 days
Time frame: 180 days
Time frame: 180 days
Time frame: 180 days
Time frame: 180 days
Time frame: 180 days
Time frame: 180 days
Time frame: 180 days
Time frame: 180 days
Time frame: 180 days
Time frame: 180 days
Time frame: 180 days
Time frame: 180 days
Time frame: 180 days
Time frame: 180 days
Time frame: 180 days
Time frame: Screening + Baseline (V1), 3 months (V2), 6 months (V3)
The Modified Ashworth Scale (MAS) is a clinical tool for assessing muscle spasticity in patients, particularly those with neurological conditions such as multiple sclerosis (MS). It assesses the resistance of a muscle to passive stretching and thus measures the degree of spasticity. The MAS helps to assess the severity of spasticity and monitor the effectiveness of treatment and disease progression. The scale ranges from 0 (no increased muscle tone) to 5 (limbs rigid in flexion and extension).
Time frame: Screening + Baseline (V1), 3 months (V2), 6 months (V3)
WHOQoL-BREF (World Health Organization Quality of Life Questionnaire Brief Version): The WHOQOL-BREF questionnaire measures quality of life across 4 domains: Physical health, psychological health, social relationships and environment. It also includes one question on overall QOL and one on general health. The WHOQOL-BREF scores correlate highly (.89 or above) with WHOQOL-100 scores, and demonstrate good discriminant validity, content validity, internal consistency and test-retest reliability. The four WHOQOL-BREF domain scores will be used as main outcome measure. The measure is calculated by summing the point values for the questions corresponding to each domain and then transforming the scores to a 0-100 point interval, with higher scores corresponding to greater QOL.
Time frame: Screening + Baseline (V1), 3 months (V2), 6 months (V3)
The Expanded Disability Status Scale (EDSS) is a scale used to measure the severity of disability in patients with multiple sclerosis (MS). It assesses neurological function based on factors such as mobility, coordination, vision and strength. The scale ranges from 0 (no disability) to 10 (death due to MS). The EDSS is used to track disease progression and make treatment decisions, with higher scores indicating greater disability.
Time frame: 6 months (V3)
Questionnaire about smartwatch usage. Patients are presented with 17 statements about the smartwatches, focusing on practicality, usability, and everyday suitability. They can score each statement from 1 to 5, where 5 means strong agreement and 1 means strong disagreement.
Time frame: Screening + Baseline (V1), 3 months (V2), 6 months (V3)
The End-of-dose-phenomena-Questionnaire assesses the effectiveness of a treatment at the end of its dosing interval and asks about an increase in symptoms. Patients can state whether they have experienced a worsening of symptoms in recent weeks and, if so, for how many days and which migraine symptoms have worsened.
Time frame: Screening + Baseline (V1), 3 months (V2), 6 months (V3)
The McCorkle and Young Symptom Distress Scale is an instrument for assessing the degree of distress caused by various physical symptoms. The scale consists of 13 symptoms (such as pain, nausea, fatigue, insomnia and shortness of breath) that are commonly experienced by patients. Patients rate each symptom on a scale of 1 to 5, with 1 being 'no distress' and 5 being 'extreme distress'. This scale can be used to determine which symptoms are the most distressing. This enables better symptom management and customised measures to improve the patient's quality of life.
Time frame: Screening + Baseline (V1), 3 months (V2), 6 months (V3)
The Multiple Sclerosis Impact Scale 29 (MSIS-29) is a questionnaire of the impact of multiple sclerosis (MS) on patients' daily lives. It consists of 29 items divided into two sections: the physical impact (20 items) and the psychological impact (9 items) of MS. Each item is rated on a scale of 1 to 5, with a higher score indicating a greater impact. The MSIS-29 helps assess how MS affects physical function and emotional well-being and provides valuable insights for treatment planning and monitoring disease progression.
Time frame: Screening + Baseline (V1), 3 months (V2), 6 months (V3)
The NRS is another tool used to assess pain intensity. It involves the patient rating their pain on a scale from 0 to 10, where 0 means "no pain" and 10 means "worst pain imaginable." Both scales are widely used due to their simplicity and effectiveness in monitoring symptom severity.
Time frame: Screening + Baseline (V1), 3 months (V2), 6 months (V3)
The Montgomery-Asberg Depression Rating Scale (MADRS) is a clinical instrument for assessing the severity of depression in patients. It consists of 10 items that assess symptoms such as mood, guilt, sleep, appetite and concentration. Each item is scored on a scale from 1 to 7, with higher scores indicating more severe depression. The MADRS is commonly used to monitor changes in depressive symptoms and evaluate the effectiveness of treatment.
Time frame: Screening + Baseline (V1), 3 months (V2), 6 months (V3)
The Edmonton Symptom Assessment Scale (ESAS) is an instrument commonly used to assess the severity of symptoms in patients with advanced or terminal illnesses. It helps to assess the intensity of symptoms such as pain, fatigue, nausea, depression, anxiety, sleep disturbance, loss of appetite, breathlessness, general well-being and physical decline. Patients rate each symptom on a scale from 0 (no symptom) to 10 (worst possible symptom), which allows for quick and effective symptom monitoring. This scale helps to adjust treatment plans and improve the quality of care by tracking changes in symptoms over time.
Time frame: Screening + Baseline (V1), 3 months (V2), 6 months (V3)
The Sleep-Questionnaire contain the Pittsburgh Sleep Quality Index (PSQI) as well as two Items on the perceived impact of the smartwatch on the patient´s sleep. The PSQI assesses the quality of sleep over a one-month interval and measures seven component scores: sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, use of sleep medication, and daytime dysfunction. Total score ranges from 0 to 21, with higher scores indicating a poorer sleep quality.
Time frame: Screening + Baseline (V1), 3 months (V2), 6 months (V3)
EQ-5D-5L: is a standardized instrument for measuring health-related quality of life. It assesses five dimensions of health: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Each dimension has five levels of severity, ranging from no problems to extreme problems. Respondents rate their health state by selecting the most appropriate level for each dimension.
Contact information is provided by the study sponsor or research team.
Heinrich-Heine University, Duesseldorf
Other
Smart Monitoring Assessing Spasticity-related Health - A Prospective Multiple Sclerosis Study With Wearables
Acronym: SMASH
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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