رادار التجارب AI | ||
|---|---|---|
حالة التجربة السريرية NCT04816006 (BRAIN) لـ سرطان الثدي، أورام الثدي، المرحلة التشريحية الأولى لسرطان الثدي AJCC v8، المرحلة التشريحية الثانية لسرطان الثدي AJCC v8، المرحلة التشريحية الثالثة أ لسرطان الثدي AJCC v8، Cancer-related Cognitive Dysfunction هي قيد التجنيد. 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
العودة إلى البحث
مايو كلينكBreast Cancer, Reasoning, and Activity Intervention (BRAIN)
تفاصيل التجربة السريرية متاحة بشكل أساسي باللغة الإنجليزية. ومع ذلك، يمكن لـ 'رادار التجارب AI' أن يساعدك؛ ما عليك سوى النقر على 'وصف الدراسة' لعرض ومناقشة معلومات التجربة باللغة التي اخترتها.
التجربة السريرية NCT04816006 (BRAIN) هي دراسة تدخُّلية لـسرطان الثدي، أورام الثدي، المرحلة التشريحية الأولى لسرطان الثدي AJCC v8، المرحلة التشريحية الثانية لسرطان الثدي AJCC v8، المرحلة التشريحية الثالثة أ لسرطان الثدي AJCC v8، Cancer-related Cognitive Dysfunction وهي قيد التجنيد. بدأت في ١٢ شعبان ١٤٤٥ هـ مع خطة لتجنيد ١٦٠ مشاركًا. يقودها مايو كلينك، ومن المتوقع اكتمالها بحلول ٢٧ صفر ١٤٤٩ هـ. تم تحديث البيانات الأخيرة من ClinicalTrials.gov في ٧ صفر ١٤٤٧ هـ.
الملخص
This phase II trial tests whether an exercise intervention works to improve cognitive function in breast cancer survivors. Many breast cancer survivors report cancer-related cognitive impairment, which this has recently become a priority in clinical research due to its dramatic impact on daily functioning, quality of life, and long-term health. Aerobic exercise has the potential to improve cognitive function and brain health in older adults and is recommended as a safe, tolerable, and accessible complementary therapy for breast cancer survivors. This study aims to understand the effects of physical activity compared with health education on memory, attention, and brain health in women with breast cancer. Study findings may help researchers design more programs that can improve memory, attention, and brain health in other women with breast cancer.
وصف مفصل
PRIMARY OBJECTIVES:
I. Examine the effectiveness of a 6-month, community-based aerobic exercise intervention on multiple indicators of cognitive function in breast cancer survivors (BCS) aged 50 and older (N=160).
II. Gather information on the intervention's potential for scalability using the Reach Effectiveness Adoption Implementation Maintenance (RE-AIM) framework.
EXPLORATORY OBJECTIVES:
I. Explore potential moderators and mediators of the effects of aerobic exercise training on cognitive function.
II. Investigate the feasibility of urinary metabolites as biomarkers of overall diet patterns.
OUTLINE: Patients are randomized to 1 of 2 arms.
ARM I: Patients attend 3 weekly exercise sessions over 60-75 minutes per week in weeks 1-2, 2 sessions over 70-70 each week in weeks 3-4, 1 session over 90-120 minutes each week in weeks 5-8, biweekly sessions over 120-150 per week across weeks 9-16, and monthly sessions over at least 150 minutes per week in weeks 17-24 for a total of 20 supervised sessions. Patients undergo a gait assessment and magnetic resonance imaging (MRI), as well as wear an accelerometer throughout the study.
ARM II: Patients participate in up to 9 monthly classes/webinars. Patients also receive informational portable document format (pdfs), videos, and/or podcasts, and a one-year subscription to the Mayo Clinic Health Letter. Patients undergo a gait assessment and MRI, as well as wear an accelerometer throughout the study.
After completion of study intervention, patients are followed up with at 6 months.
العنوان الرسمي
Enhancing Cognitive Function in Breast Cancer Survivors Through Community-based Exercise Training
الحالات الطبية
سرطان الثديأورام الثديالمرحلة التشريحية الأولى لسرطان الثدي AJCC v8المرحلة التشريحية الثانية لسرطان الثدي AJCC v8المرحلة التشريحية الثالثة أ لسرطان الثدي AJCC v8Cancer-related Cognitive Dysfunctionالمنشورات
مقالات علمية وأوراق بحثية منشورة حول هذه التجربة السريرية:معرّفات دراسة أخرى
- BRAIN
- MC231001
- 23-000020 (معرف آخر) (Mayo Clinic Institutional Review Board)
- 852-20-FB (معرف آخر) (Previous IRB)
- R37CA252060 (منحة/عقد NIH الأمريكي)
- NCI-2021-09939 (معرف السجل) (Clinical Trials Reporting Program)
NCT معرّف
تاريخ البدء (فعلي)
2024-02-22
آخر تحديث مُنشور
2025-08-01
تاريخ الاكتمال (المقدر)
2027-07-31
عدد المشاركين المخطط لهم
١٦٠
نوع الدراسة
تدخُّلية
المرحلة
غ/م
الحالة
قيد التجنيد
الكلمات الرئيسية
physical activity
exercise
cognition
brain health
breast cancer
exercise
cognition
brain health
breast cancer
الغرض الأساسي
الرعاية الداعمة
طريقة توزيع المشاركين
عشوائي
نموذج التدخل
التصميم المتوازي
التعمية
مزدوج
مجموعات/التدخلات
| مجموعة المشاركين/مجموعة | تَدَخُّل/علاج |
|---|---|
تجريبيةArm I (Aerobic Exercise) Patients attend 3 weekly exercise sessions over 60-75 minutes per week in weeks 1-2, 2 sessions over 70-70 each week in weeks 3-4, 1 session over 90-120 minutes each week in weeks 5-8, biweekly sessions over 120-150 per week across weeks 9-16, and monthly sessions over at least 150 minutes per week in weeks 17-24 for a total of 20 supervised sessions. Patients undergo MRI and wear an accelerometer throughout the study. | تدريب التمارين الهوائية Breast cancer survivors in the intervention group will participate in a 24-week moderate intensity exercise program led by community-based fitness center personal trainers. Individually-tailored exercise prescriptions will be developed based upon each participant's baseline maximal graded exercise test (heart rate corresponding with %VO2 peak) and symptom limitation. Sessions will be progressive in nature such that the volume of exercise increases across weeks. Treadmill walking is the primary mode of exercise. However, participants will be permitted to use other cardiovascular equipment (e.g., elliptical machines, stationary bicycles) as prescribed by their exercise trainer. The trainer will supervise three weekly exercise sessions in Weeks 1-2, two in Weeks 3-4, one in Weeks 5-8, biweekly across weeks 9-16, and monthly in Weeks 17-24 (N=20 supervised sessions). |
مقارن نشطArm II (Health Education) Patients participate in up to 9 monthly classes/webinars. Patients also receive informational pdfs, videos, and/or podcasts, and a one-year subscription to the Mayo Clinic Health Letter. Patients undergo a gait assessment and MRI, as well as wear an accelerometer throughout the study. | Health Education (Active Comparator) Breast cancer survivors in the Health Education group will participate in education sessions with a health educator and receive monthly newsletters/webinars (N=20 total contacts) across 24 weeks. The program will include cancer support and discussion of cancer-related wellness topics (e.g., stress management, coping). Control group participants will be offered a 6-month fitness center membership upon study completion. |
النتيجة الرئيسية
| مقياس النتيجة | وصف القياس | الإطار الزمني |
|---|---|---|
Change in inhibitory control | Change in interference score on Stroop task, with positive values indicating greater inhibitory control. | baseline (Month 0), post-intervention (month 6), follow up (month 12) |
Change in cognitive flexibility | Change in accuracy on Shifting Attention task, with higher values indicating greater cognitive flexibility | baseline (Month 0), post-intervention (month 6), follow up (month 12) |
Change in executive function processing | Change in reaction time on Shifting Attention task, with lower values indicating greater cognitive flexibility | baseline (Month 0), post-intervention (month 6), follow up (month 12) |
Change in short-term memory | Change in accuracy on Visual Memory task, with higher accuracy indicating greater short-term memory | baseline (Month 0), post-intervention (month 6), follow up (month 12) |
Change in verbal memory | Change in number recalled on Hopkins Verbal Learning task, with higher values indicating greater verbal memory | baseline (Month 0), post-intervention (month 6), follow up (month 12) |
Change in working memory | Change in reaction time the 4-part Continuous Performance task, with lower values indicating greater working memory | baseline (Month 0), post-intervention (month 6), follow up (month 12) |
Change in brain volume | Change in mean cortical thickness of brain regions of interest as measured by an anatomic MRI brain scan | baseline (Month 0), post-intervention (month 6) |
Change in white matter integrity | Change in fractional anisotropy as measured by diffusion MRI. | baseline (Month 0), post-intervention (month 6) |
Change in resting state functional connectivity | Change in within-network pairwise correlation estimates as measured using a multiband echo planar imaging (mb-EPI) functional MRI sequence | baseline (Month 0), post-intervention (month 6) |
Change in self-reported cognitive function | The perceived cognitive impairments subscale of the Functional Assessment in Cancer Therapy - Cognition (FACT-Cog) will be used to measure self-reported cognition. Scores range from 0-72, with higher scores indicating better cognitive function. | baseline (Month 0), post-intervention (month 6), follow up (month 12) |
Reach | Participation rate among eligible individuals contacted about the study. | baseline (Month 0) |
Adoption | Sociodemographics questionnaire to describe demographics characteristics and experience among personal trainers | post-intervention (month 6) |
Change in Cardiorespiratory Fitness | Change in Peak VO2 as measured by a modified Balke treadmill graded exercise test protocol. | baseline (Month 0), post-intervention (month 6), follow up (month 12) |
Change in Cancer-related Fatigue | The Functional Assessment in Chronic Illness Therapy (FACIT) - Fatigue Scale will be used to measure cancer-related fatigue. Scores range from 0-52, with higher scores indicating less cancer-related fatigue. | baseline (Month 0), post-intervention (month 6), follow up (month 12) |
Implementation | Percent of session checklist items completed as intended | post-intervention (month 6) |
Maintenance | The number of participants who withdraw during the follow-up period. | follow up (month 12) |
Change in processing speed | Change in reaction time on Symbol Digit Coding task, with lower values indicating greater processing speed | baseline (Month 0), post-intervention (month 6), follow up (month 12) |
Change in attention | Change in choice reaction time on Continuous Performance task, with lower values indicating greater sustained attention | baseline (Month 0), post-intervention (month 6), follow up (month 12) |
معايير الأهلية
الأعمار المؤهلة للدراسة
بالغ, كبار السن
العمر الأدنى للدراسة
50 Years
الجنس المؤهل
أنثى
- PRE-REGISTRATION: Age ≥50 years at time of pre-registration visit according to participant report and/or clinical determination
- PRE-REGISTRATION: First, primary diagnosis of stage I-IIIa breast cancer according to participant report and/or clinical determination
- PRE-REGISTRATION: Post-surgery and completed primary treatment (i.e., surgery, chemotherapy, and/or radiation therapy) 3-36 months prior to registration according to participant report and/or clinical determination
- PRE-REGISTRATION: Sedentary except for casual lifestyle recreation defined as self-reporting no more than 90 minutes per week of moderate-intensity aerobic exercise within the last 6 months
- PRE-REGISTRATION: Self-reported ability to complete assessments by themselves or with assistance
- REGISTRATION: Age ≥50 years as confirmed via clinical determination
- REGISTRATION: Able to provide medical record release to confirm eligibility
- REGISTRATION: First, primary diagnosis of stage I-IIIa breast cancer as confirmed via clinical determination
- REGISTRATION: Post-surgery and completed primary treatment (i.e., surgery, chemotherapy, and/or radiation therapy) 3-36 months prior to pre-registration as confirmed via clinical determination
- REGISTRATION: No evidence of possible cognitive impairment as assessed using the Telephone Interview of Cognitive status (13-item modified version) (TICS-M; score > 21) NOTE: Only individuals who pass the TICS-M during pre-registration will be invited to participate in the urine substudy
- REGISTRATION: Receive physician's clearance to participate in an exercise program
NOTE: Individuals with conditions/diagnoses deemed important by the primary investigator will be required to provide clearance for exercise from their cardiologist. Example conditions include:
History of major multiple myocardial infarctions (MI)
Recent electrocardiogram (ECG) changes or recent MI
Resting or unstable angina
Significant multivessel coronary occlusion (≥ 70%) on angiography
Uncontrolled and/or serious arrhythmias
3rd degree heart block
Acute congestive heart failure or ejection fraction < 30%
- REGISTRATION: Ability to complete assessments by themselves or with assistance
- PRE-REGISTRATION: Stage 0 breast cancer diagnosis OR metastatic disease
- PRE-REGISTRATION: Currently receiving or < 3 months since receiving chemotherapy or radiation therapy for cancer, or greater than 36 months post primary treatment
- PRE-REGISTRATION: Planned surgery during the intervention period
- PRE-REGISTRATION: Second cancer diagnosis (excluding non-invasive skin cancers or carcinoma-in-situ for any cancer)
- PRE-REGISTRATION: Unable to travel regularly to the study locations for intervention sessions and data collection
- PRE-REGISTRATION: Unwilling to return to enrolling institution for follow-up
- PRE-REGISTRATION: Self-reported inability to walk without assistance or devices
- REGISTRATION: History of stroke, transient ischemic attack, other neurological disorders, or brain surgery involving tissue removal as confirmed via clinical determination
- REGISTRATION: Clinically significant TICS-M score (< 21) during baseline procedures
- REGISTRATION: Not able to provide physician re-clearance for exercise if required based upon clinically significant baseline exercise test (as determined by ECG and blood pressure monitoring)
- REGISTRATION: Contraindications to functional magnetic resonance imaging (fMRI) in accordance with the Mayo Clinic Department of Radiology safety protocols
- REGISTRATION: Clinically significant MRI scan as determined by physician review in which the following is advised via radiologist overread: remarkable/abnormal limited diagnostic brain image with recommended medical follow-up
- REGISTRATION: Enrolled in another physical activity program
- REGISTRATION: Unable to walk without assistance or devices
- REGISTRATION: Unwilling to complete study requirements
- REGISTRATION: Unwilling to be randomized to the exercise group or health education group
- REGISTRATION: Unable or unwilling to continuously wear and regularly sync/charge an activity tracker during the study period
- REGISTRATION: Unable to travel regularly to the study locations for intervention sessions and data collection
- REGISTRATION: Unwilling to return to enrolling institution for follow-up
مايو كلينك868 تجارب سريرية نشطة للاستكشافالمعهد الوطني للسرطان3028 تجارب سريرية نشطة للاستكشافالجهة المسؤولة عن الدراسة
Diane K. Ehlers, Ph.D., المحقق الرئيسي, Principal Investigator, Mayo Clinic
جهة اتصال مركزية للدراسة
جهة اتصال: Melissa Cole, MS, 480-574-4052, [email protected]
جهة اتصال: Clinical Trials Referral Office, 855-776-0015, [email protected]
1 مواقع الدراسة في 1 بلدان
Arizona
Mayo Clinic in Arizona, Phoenix, Arizona, 85054, United States
Melissa Cole, MS, جهة اتصال, 480-574-4052, [email protected]
Clinical Trials Referral Office, جهة اتصال, 855-776-0015, [email protected]
Diane K. Ehlers, Ph.D., المحقق الرئيسي
قيد التجنيد