Mobile Cognitive Behavioral Therapy for Stroke
Ориентир для пациента и семьи
Простыми словами
Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.
- Что изучают
- В протоколе указаны: Mobile CBT for Stroke.
- Кому может быть актуально
- Состояния в реестре: Anxiety, Stroke, Depression. Базовые параметры: 40 лет — 79 лет · Все.
- Что важно проверить
- Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
- Где проводится
- США
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
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Обзор
This study aims to assess the feasibility and acceptability of "MAYA", a mobile cognitive behavioral therapy app for anxiety and mood disorders, in adults who have had a stroke.
Подробное описание
The primary objective of this study is to assess the feasibility and acceptability of "MAYA", a mobile CBT application, in adults who have had a stroke. Feasibility will be measured by the total number of sessions completed and acceptability will be measured by scores on the Mobile Application Rating Scale-User Version (uMARS). Qualitative feedback will also be collected with a questionnaire using open-ended questions.
A secondary objective will be to evaluate preliminary efficacy of the mobile CBT application on symptoms of depression and anxiety assessed using (1) interview-based measures (the Montgomery Asberg Depression Rating Scale \[MADRS\] and the Hamilton Anxiety Rating Scale \[HAM-A\]), and (2) a patient reported outcome measure (the 21-item Depression, Anxiety, and Stress Scale \[DASS\]).
This study will collect pilot data over the course of 8 weeks. Because this is a pilot study, all participants will use the same version of the app and there will be no control group. Primary outcome measures will be collected at baseline (pre-intervention) and at the endpoint (week 8). Participants will be asked to use the mobile app for at least two days a week, for 30 minutes on each day, for 8 weeks. Participants will have weekly check-ins in person or via a HIPAA compliant virtual meeting platform (Zoom) with a study staff member to assess intervention adherence and answer brief questionnaires designed to assess feasibility, acceptability, and mood symptoms.
Вмешательства
- Устройство Mobile CBT for Stroke
A mobile cognitive behavioral therapy (CBT) app called "Maya" that includes modules with educational content and teaching and practice of strategies that address depression and anxiety after stroke.
Первичные конечные точки
- Feasibility and Acceptability of MAYA as measured by the Mobile Application Rating Scale-User Version (uMARS) [Срок оценки: Week 4 of treatment]
- Feasibility and Acceptability of MAYA as measured by the Mobile Application Rating Scale-User Version (uMARS) [Срок оценки: Week 8 of treatment]
- Number of Sessions completed over study time period [Срок оценки: Week 1 to Week 8 (8 week treatment)]
- Qualitative Interview [Срок оценки: Week 8 of treatment]
Вторичные конечные точки (3)
- Change in depression symptoms, as measured by the Montgomery Asberg Depression Rating Scale (MADRS) [Срок оценки: Baseline, Week 4, and Week 8 of treatment (8 week treatment)]
- Change in anxiety symptoms, as measured by the Hamilton Anxiety Rating Scale (HAM-A) [Срок оценки: Baseline, Week 4, and Week 8 of treatment (8 week treatment)]
- Change in depression, anxiety, and stress, as measured by the Depression, Anxiety, and Stress Scale (DASS) [Срок оценки: Baseline, Week 4, and Week 8 of treatment (8 week treatment)]
Критерии участия
Критерии включения
- Age 40-79
- Presence of clinically-significant anxiety and/or depression (as determined by an eligibility evaluation)
- Stroke that occurred 1 month or more prior to study initiation
- Capacity to provide consent
- No greater than mild cognitive difficulties based on an eligibility evaluation conducted as part of the study
- If taking medication for depression and/or anxiety, must be on a stable dose for a minimum of 8 weeks prior to study initiation
- Ability to use iPhone or iPad independently
- Home internet access
- Willingness to participate in the full study duration.
Критерии исключения
- Aphasia of moderate or greater severity (as determined during an eligibility evaluation)
- Non-fluency in English
- History of a bipolar or psychotic disorder
- Current alcohol or substance use disorder
- Active suicidal ideation
- Current engagement in psychotherapy is not grounds for exclusion unless the individual's psychotherapy is primarily focused on CBT
- Severe depression and/or anxiety based on the initial evaluation and clinical judgment of the study doctor, which warrants a higher level of care and/or immediate referral to psychiatric services
- Any other clinical or medical reason in the study doctor's initial screening evaluation that suggests the study is not appropriate for the participant
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Распределение
- Не применимо
- Модель
- Одна группа
- Маскирование
- Открытое
- Основная цель
- Лечение
Центры проведения
США · 1 центр
- Weill Cornell Medicine — New York
Публикации
- Wilhelm S, Weingarden H, Ladis I, Braddick V, Shin J, Jacobson NC. Cognitive-Behavioral Therapy in the Digital Age: Presidential Address. Behav Ther. 2020 Jan;51(1):1-14. doi: 10.1016/j.beth.2019.08.001. Epub 2019 Aug 8. PMID 32005328
- Wang SB, Wang YY, Zhang QE, Wu SL, Ng CH, Ungvari GS, Chen L, Wang CX, Jia FJ, Xiang YT. Cognitive behavioral therapy for post-stroke depression: A meta-analysis. J Affect Disord. 2018 Aug 1;235:589-596. doi: 10.1016/j.jad.2018.04.011. Epub 2018 Apr 5. PMID 29704854
- Wada Y, Otaka Y, Yoshida T, Takekoshi K, Takenaka R, Senju Y, Maeda H, Shibata S, Kishi T, Hirano S. Effect of Post-stroke Depression on Functional Outcomes of Patients With Stroke in the Rehabilitation Ward: A Retrospective Cohort Study. Arch Rehabil Res Clin Transl. 2023 Aug 2;5(4):100287. doi: 10.1016/j.arrct.2023.100287. eCollection 2023 Dec. PMID 38163038
- Bress JN, Falk A, Schier MM, Jaywant A, Moroney E, Dargis M, Bennett SM, Scult MA, Volpp KG, Asch DA, Balachandran M, Perlis RH, Lee FS, Gunning FM. Efficacy of a Mobile App-Based Intervention for Young Adults With Anxiety Disorders: A Randomized Clinical Trial. JAMA Netw Open. 2024 Aug 1;7(8):e2428372. doi: 10.1001/jamanetworkopen.2024.28372. PMID 39163044
- Mitchell AJ, Sheth B, Gill J, Yadegarfar M, Stubbs B, Yadegarfar M, Meader N. Prevalence and predictors of post-stroke mood disorders: A meta-analysis and meta-regression of depression, anxiety and adjustment disorder. Gen Hosp Psychiatry. 2017 Jul;47:48-60. doi: 10.1016/j.genhosppsych.2017.04.001. Epub 2017 Apr 3. PMID 28807138
- Ahrens J, Shao R, Blackport D, Macaluso S, Viana R, Teasell R, Mehta S. Cognitive -behavioral therapy for managing depressive and anxiety symptoms after stroke: a systematic review and meta-analysis. Top Stroke Rehabil. 2023 May;30(4):368-383. doi: 10.1080/10749357.2022.2049505. Epub 2022 Mar 30. PMID 35352629
Идентификаторы
NCT: NCT06689878 · 24-04027396