- ICH GCP
- Реестр клинических исследований США
- Клиническое испытание NCT01110993
An Observational Study to Evaluate Quality of Life (QoL) and Influence of Cognitive Status on QoL in Patients With Relapsing-Remitting Multiple Sclerosis (RRMS) During 2 Years Treatment With Rebif New Formulation (RNF) (MusiClock)
Prospective, Non-interventional, Multicenter Study to Evaluate QoL and Influence of Cognitive Status on QoL in Patients With RRMS During 2 Years Treatment With RNF
Обзор исследования
Статус
Подробное описание
Multiple sclerosis (MS) is an acquired demyelinating disease of unclear etiology, occurring mainly in adults. Multiple sclerosis occurs in 30-100 people per 100 000. Usually the disease attacks young adults aged between 20 and 40 years. The peak of this occurrence is in the population of 30-35 year olds.
The main feature of the disease is multifocal (disseminated) injury of the central nervous system. The injury causes various neurological symptoms and signs that go on and off (relapsing-remitting form) or progress steadily, and with time cause irreversible damage of the nervous system and permanent disability. In neuropsychological studies, 40-65% of MS subjects show cognitive impairment with prominent involvement of memory, sustained attention and information processing speed. Multiple sclerosis subjects with different disease courses have different cognitive profiles.
Cognitive dysfunction can have a dramatic impact on a subject's QoL, influencing the fulfillment in work and social life, independently from physical disability. The methodology of cognitive status assessment in MS is based on established sets of tests, which could be conduced by qualified neurophysiologists. There is a need of simple test that could be quickly conducted by every physician, providing information of cognitive status/ or one of its parameters (attention/concentration). That kind of information could be immediately used by the physician during the visit to adjust the way of taking history or giving advices to subjects.
During the last 10 years there's been an enormous progress in the MS treatment. New drugs appeared that proved to diminish clinical activity of the disease and slow its progress. Early treatment with disease modifying therapies may reduce cognitive impairment or slow down the progression of cognitive deficits.
The scope of this study is to evaluate the cognitive status (attention/concentration) and the influence of cognitive impairment on QoL in subjects with RRMS during two years of treatment with RNF.
OBJECTIVES
Primary objective:
- To evaluate the QoL in subjects with RRMS during two years of treatment with RNF
Secondary objectives:
- To evaluate the cognitive status (attention/concentration) and the influence of cognitive impairment on QoL in subjects with RRMS during two years of treatment with RNF Subjects will be treated according to widely-acknowledged standards for MS treatment and the choice of drug will depend solely on medical indications. The potential subjects will have been prescribed Rebif for the first time by their treating physicians and will then be given the option to enter in this observational study. As this is purely an observational study, the subjects will be followed by their treating physicians, according to current medical practice and Rebif SmPC (Summary of Product Characteristics) requirements (i.e monitoring of thyroid and liver enzymes prior to the start of therapy, and hepatic function at months 1, 3, 6 and periodically thereafter, prescription of antipyretics etc.) After each control visit, the treating physician will complete subject's observations chart. The planned schedule of visits will be identical to the routine schedule of control visits dictated by the National Health Found: 1st Visit - 3 months after RNF therapy start, 2nd Visit - after 6 months, 3rd Visit - after 9 months, 4th Visit - after 12 months, 5th Visit - after 18 months, 6th Visit - after 24 months.
"0" visit - doctors will be asked to complete data from subjects history (doctors will be given the proposal of testing (MusiQoL[Multiple Sclerosis International Quality of Life], MMSE [Mini Mental State Examination] and 10-PCT [10-Point Clock Test]) most subjects on the visit when the disease-modifying drugs [DMD] therapy is instituted).
Тип исследования
Регистрация (Действительный)
Контакты и местонахождение
Места учебы
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Lublin, Польша
- Medical University, Department of Neurology
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Критерии участия
Критерии приемлемости
Возраст, подходящий для обучения
Принимает здоровых добровольцев
Полы, имеющие право на обучение
Метод выборки
Исследуемая популяция
Описание
There are no specific inclusion/exclusion criteria as the trial is a non-interventional, observational study. The criteria are based on SmPC and criteria of Polish National Found Programme of RRMS Patients Treatment:
Inclusion Criteria:
- Subjects aged above 18 years
- Subjects with clinically diagnosed RRMS which is characterised by two or more acute exacerbations in the previous two years
- Subjects who has never been treated with Rebif (previous treatment with other DMDs will not be regarded as an exclusion criterion)
- Written consent to cooperation made by the environmental nurse who takes care about subject in hospital as well as in his home
- Score of 21 or more points, according to National Heath Found Patient inclusion criteria for the 2 years program of MS treatment with interferon beta
Exclusion Criteria:
Exclusion criteria conform with Rebif's registered contraindications, described in an Sm PC approved by Ministry of Health.
- Interferon beta-1a is contraindicated during pregnancy
- Interferon beta-1a is contraindicated in subjects with confirmed hypersensitivity to natural or recombined interferon beta, or to any of the adjuvant substances
- Interferon beta-1a is contraindicated in subjects with severe depression and/or suicidal thoughts
Учебный план
Как устроено исследование?
Детали дизайна
- Наблюдательные модели: Когорта
- Временные перспективы: Перспективный
Что измеряет исследование?
Первичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
---|---|---|
Quality of Life
Временное ограничение: Baseline to 24 months of RNF treatment (At baseline, 12 and 24 months)
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To evaluate the QoL by assessing the changes in MusiQoL Questionaire scores
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Baseline to 24 months of RNF treatment (At baseline, 12 and 24 months)
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Вторичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
---|---|---|
Assessment of Cognitive Status
Временное ограничение: Baseline to 24 months of RNF treatment (At baseline, 12 and 24 months)
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To evaluate cognitive status by assessing the changes in MMSE and 10-PCT scores
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Baseline to 24 months of RNF treatment (At baseline, 12 and 24 months)
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Influence of cognitive impairment on QoL in subjects with RRMS
Временное ограничение: Baseline to 24 months of RNF treatment (At baseline, 12 and 24 months)
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To evaluate the influence of cognitive impairment on QoL in subjects with RRMS by assessing the correlation between changes in MusiQoL and those in 10-PCT and MMSE
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Baseline to 24 months of RNF treatment (At baseline, 12 and 24 months)
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Assessment of Expanded Disability Status Scale
Временное ограничение: Baseline to 24 months of RNF treatment (At baseline, 12 and 24 months)
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Baseline to 24 months of RNF treatment (At baseline, 12 and 24 months)
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Assessment of number of relapses
Временное ограничение: Baseline to 24 months of RNF treatment (At baseline, 12 and 24 months)
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Baseline to 24 months of RNF treatment (At baseline, 12 and 24 months)
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Assessment of results of Evoked Potentials (visual, auditory, somatosensory/ if they are routinely done)
Временное ограничение: Baseline to 24 months of RNF treatment (At baseline, 12 and 24 months)
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Baseline to 24 months of RNF treatment (At baseline, 12 and 24 months)
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Assessment of Magnetic Resonance Imaging results
Временное ограничение: Baseline to 24 months of RNF treatment (At baseline, 12 and 24 months)
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MRI results will be assessed to depict new Gd-enhancing lesions, new T2 lesions, enlarging T2 (BOD) lesions, new T1 hypointense lesions, enlarging T1 hypointense lesions, atrophy /if they are routinely done
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Baseline to 24 months of RNF treatment (At baseline, 12 and 24 months)
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Соавторы и исследователи
Спонсор
Следователи
- Главный следователь: Zbigniew Stelmasiak, Prof., Medical University, Department of Neurology, Lublin, Poland
Даты записи исследования
Изучение основных дат
Начало исследования
Первичное завершение (Действительный)
Завершение исследования (Действительный)
Даты регистрации исследования
Первый отправленный
Впервые представлено, что соответствует критериям контроля качества
Первый опубликованный (Оценивать)
Обновления учебных записей
Последнее опубликованное обновление (Оценивать)
Последнее отправленное обновление, отвечающее критериям контроля качества
Последняя проверка
Дополнительная информация
Термины, связанные с этим исследованием
Ключевые слова
Дополнительные соответствующие термины MeSH
Другие идентификационные номера исследования
- EMR 701068-516
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