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رادار التجارب AI
حالة التجربة السريرية NCT06445192 لـ سرطان الرئة 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

Evaluating the Impact of a Virtually Supervised Exercise Intervention and Group Counseling on Inflammation and the Microbiome of Smokers at High Risk for Lung Cancer, BE FIT Trial

قيد التجنيد
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 NCT06445192 هي دراسة تدخُّلية لـسرطان الرئة وهي قيد التجنيد. بدأت في ١٩ ربيع الآخر ١٤٤٥ هـ مع خطة لتجنيد ٨٨ مشاركًا. يقودها جامعة ولاية أوهايو، ومن المتوقع اكتمالها بحلول ١١ رجب ١٤٤٧ هـ. تم تحديث البيانات الأخيرة من ClinicalTrials.gov في ٧ ذو الحجة ١٤٤٦ هـ.
الملخص
This phase II trial evaluates how a virtually supervised exercise intervention in combination with group counseling affects inflammation and the bacterial composition (microbiome) of the gut in smokers who are at high risk for lung cancer. Physical exercise has been shown to reduce lung cancer development and to have beneficial effects on the gut microbiome and inflammation. Group counseling may promote adherence to the exercise intervention by empowering participants to exert greater control over their behavior and environment. This clinical trial may help researchers understand how exercise impacts inflammation and the microbiome in people at risk for lung cancer and whether or not exercise with counseling can improve health outcomes in high-risk individuals.
وصف مفصل
PRIMARY OBJECTIVES:

I. To evaluate the feasibility and preliminary efficacy of establishing a multi-component virtually-delivered exercise intervention trial with longitudinal biomarker and microbiome collection in the Ohio State University Lung Cancer Screening Clinic (OSULCSC).

II. To determine the impact of the multi-component virtually-delivered exercise intervention on the microbiome and inflammatory biomarkers.

OUTLINE: Participants are randomized to 1 of 2 groups.

GROUP I: Participants receive the supervised aerobic and resistance exercise intervention over 1 hour via telehealth twice a week (BIW) in weeks 1-8 and once a week (QW) in weeks 9-12 and then continue with unsupervised exercise sessions BIW in weeks 13-52. Participants also attend group counseling sessions over 1 hour QW in weeks 1-8 and bi-weekly in weeks 9-12. Participants also wear a Fitbit throughout the trial and undergo collection of blood samples at baseline and follow up.

GROUP II: Participants receive usual care consisting of education on standard recommendations for physical activity, the benefits of exercise, and an example of a light walking program. Participants also wear a Fitbit throughout the trial and undergo collection of blood samples at baseline and follow up.

After completion of study intervention, participants are followed up at 12 weeks and 1 year.

العنوان الرسمي

The BE FIT Study: Feasibility of an Exercise Intervention on Microbiome and Immune Function in a High-Risk Cohort for Lung Cancer

الحالات الطبية
سرطان الرئة
معرّفات دراسة أخرى
NCT معرّف
تاريخ البدء (فعلي)
2023-11-03
آخر تحديث مُنشور
2025-06-03
تاريخ الاكتمال (المقدر)
2025-12-31
عدد المشاركين المخطط لهم
٨٨
نوع الدراسة
تدخُّلية
المرحلة
غ/م
الحالة
قيد التجنيد
الغرض الأساسي
وقاية
طريقة توزيع المشاركين
عشوائي
نموذج التدخل
التصميم المتوازي
التعمية
أحادي
مجموعات/التدخلات
مجموعة المشاركين/مجموعةتَدَخُّل/علاج
تجريبيةGroup I (exercise intervention)
Participants receive the supervised aerobic and resistance exercise intervention over 1 hour via telehealth BIW in weeks 1-8 and QW in weeks 9-12 and then continue with unsupervised exercise sessions BIW in weeks 13-52. Participants also attend group counseling sessions over 1 hour QW in weeks 1-8 and bi-weekly in weeks 9-12. Participants also wear a Fitbit throughout the trial and undergo collection of blood samples at baseline and follow up.
جمع العينات البيولوجية
Undergo collection of blood samples
إرشاد التمارين
Attend group counseling
تدخل التمارين
Receive aerobic and resistance exercise intervention via telehealth
استخدام وتقييم الأجهزة الطبية
Wear Fitbit
اختبار الأداء البدني
Ancillary studies
إدارة الاستبيان
Ancillary studies
الطب عن بعد
Receive aerobic and resistance exercise intervention via telehealth
مقارن نشطGroup II (usual care)
Participants receive usual care consisting of education on standard recommendations for physical activity, the benefits of exercise, and an example of a light walking program. Participants also wear a Fitbit throughout the trial and undergo collection of blood samples at baseline and follow up.
أفضل الممارسات
Receive usual care
جمع العينات البيولوجية
Undergo collection of blood samples
استخدام وتقييم الأجهزة الطبية
Wear Fitbit
اختبار الأداء البدني
Ancillary studies
إدارة الاستبيان
Ancillary studies
النتيجة الرئيسية
مقياس النتيجةوصف القياسالإطار الزمني
Number of patients recruited to virtually-delivered exercise intervention (feasibility)
To evaluate the feasibility and preliminary efficacy of establishing a multi-component virtually-delivered exercise intervention trial with longitudinal biomarker and microbiome collection in the Ohio State University Lung Cancer Screening Clinic (OSULCSC)
Up to 1 year
Proportion of patients who achieve study adherence (feasibility) based on attendance to the exercise program sessions and biospecimens submitted.
Study adherence is defined as a) the proportion of patients attending at least 20 out of 24 sessions for the 12-week program and b) the percentage of biospecimen samples collected at the post program period (12 weeks). This study will be considered feasible if the compliance rate for both of these combined is 75% or more. Descriptive statistics will be used to examine the distribution of all patient and treatment characteristics, including compliance.
During 12-week program
Assess the number of participants with a change in inflammatory biomarkers
Will assess the effect of the intervention on inflammatory markers of C-reactive protein and IL-6 separately using linear mixed models with the biomarker serving as the outcome variable. Will also assess the changes in the biomarkers across time in each intervention group.
Baseline to post-intervention (12 weeks)
Microbe relative abundances
Will assess the effect of the intervention on the diversity and relative abundances of individual microbes. Will compare everyone's post-intervention time point to baseline in control and the exercise interventions cohorts, applying linear or generalized mixed-effects models for the diversity or individual microbes.
Baseline to post-intervention (12 weeks)
معايير الأهلية

الأعمار المؤهلة للدراسة
بالغ, كبار السن
العمر الأدنى للدراسة
40 Years
الجنس المؤهل
الكل
يقبل المتطوعين الأصحاء
نعم
  • 50-77 years of age
  • Current or former smoker with 20-pack year smoking history and within the last 15 years
  • Fewer than 150 minutes of participation in moderate intensity physical activity each week
  • All participants must be free of severe heart, respiratory (e.g. chronic obstructive pulmonary disease [COPD]), or systemic disease that would make moderate intensity exercise participation unsafe
  • Willing to sign an informed consent

  • Person undergoing treatment for cancer in any form
  • Person plans to enter smoking cessation or change status
الجهة المسؤولة عن الدراسة
Marisa Bittoni, المحقق الرئيسي, Principal Investigator, Ohio State University Comprehensive Cancer Center
جهة اتصال مركزية للدراسة
جهة اتصال: The Ohio State Comprehensive Cancer Center, 800-293-5066, [email protected]
1 مواقع الدراسة في 1 بلدان

Ohio

Ohio State University Comprehensive Cancer Center, Columbus, Ohio, 43210, United States
Marisa Bittoni, PhD, جهة اتصال, 614-206-3518, [email protected]
Marisa Bittoni, PhD, المحقق الرئيسي
قيد التجنيد