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حالة التجربة السريرية NCT06554717 (TRIUMPH) لـ عدوى HIV-1، الضعف، Impaired Physical Function، سمنة بطنية، الشيخوخة 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

Tesamorelin as an Adjunct to Exercise for Improving Physical Function in HIV (TRIUMPH)

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 NCT06554717 (TRIUMPH) مصممة لدراسة علاج لـعدوى HIV-1، الضعف، Impaired Physical Function، سمنة بطنية، الشيخوخة. إنها تجربة تدخُّلية من المرحلة الثانية وهي قيد التجنيد. بدأت في ١٢ محرم ١٤٤٧ هـ مع خطة لتجنيد ١٠٠ مشاركًا. تقودها Massachusetts General Hospital، ومن المتوقع اكتمالها بحلول ٧ صفر ١٤٥٠ هـ. تم تحديث البيانات الأخيرة من ClinicalTrials.gov في ٤ صفر ١٤٤٧ هـ.
الملخص
People with HIV experience earlier impairments in physical function compared to people in the general population. They also exhibit an earlier presentation and more rapid development of frailty, a multisystemic syndrome of aging characterized by reduced activity, fatigue, slowness, weakness, and weight loss. While exercise can improve physical function in people with HIV, it is less effective in doing so than in the general population and is difficult to sustain in the long-term.

The goal of this clinical trial is to learn whether the medication tesamorelin will improve physical function and muscle health in adults with HIV when combined with exercise. Tesamorelin is a growth hormone-releasing hormone analogue that is FDA-approved to treat abdominal fat accumulation in people with HIV. While tesamorelin has also been shown to increase muscle mass and improve measures of muscle health, its effects on physical performance and muscle strength have not yet been evaluated.

During a 24-week intervention phase, half of participants will be randomly assigned to receive tesamorelin and half of participants will be randomly assigned to receive placebo (a look-alike substance that contains no drug). All participants also will engage in a home-based exercise intervention supervised by an exercise coach. During a subsequent 24-week extension phase, individuals will be monitored off study drug and supervised exercise, and be encouraged to continue to exercise independently.

The investigators will investigate effects of tesamorelin on physical function, muscle mass and quality, quality of life, and exercise adherence and self-efficacy. They also will evaluate whether effects of tesamorelin are maintained following treatment cessation. This study may identify an important strategy to improve how individuals aging with HIV function and feel with potential applications to other patient populations.

العنوان الرسمي

Tesamorelin as an Adjunct to Exercise for Improving Physical Function in HIV

الحالات الطبية
عدوى HIV-1الضعفImpaired Physical Functionسمنة بطنيةالشيخوخة
معرّفات دراسة أخرى
  • TRIUMPH
  • 2024P001703
NCT معرّف
تاريخ البدء (فعلي)
2025-07-07
آخر تحديث مُنشور
2025-07-29
تاريخ الاكتمال (المقدر)
2028-06-30
عدد المشاركين المخطط لهم
١٠٠
نوع الدراسة
تدخُّلية
المرحلة
المرحلة الثانية
الحالة
قيد التجنيد
الغرض الأساسي
العلاج
طريقة توزيع المشاركين
عشوائي
نموذج التدخل
التصميم المتوازي
التعمية
رباعي
مجموعات/التدخلات
مجموعة المشاركين/مجموعةتَدَخُّل/علاج
مقارن نشطTesamorelin Plus Exercise
Tesamorelin WR 1.28 mg given subcutaneously daily plus home-based semi-supervised exercise intervention
Tesamorelin
Tesamorelin WR 1.28 mg given subcutaneously daily
تمرين
Home-based semi-supervised exercise program
مقارن بالدواء الوهميPlacebo Plus Exercise
Identical placebo given subcutaneously daily plus home-based semi-supervised exercise intervention
دواء وهمي
Identical placebo injection given subcutaneously daily
تمرين
Home-based semi-supervised exercise program
النتيجة الرئيسية
مقياس النتيجةوصف القياسالإطار الزمني
Change in Repeated Chair Stand Time
Time to complete 10 repeated chair stands
Baseline to Week 24
النتيجة الثانوية
مقياس النتيجةوصف القياسالإطار الزمني
Change in Standard and Modified Short Physical Performance Battery (SPPB)
Objective assessment of physical function that includes measures of balance, gait, and strength
Baseline to Week 24
Change in 1-Repetition Maximum Leg Press
Maximal weight that can be lifted by lower extremities once using correct form through full range of motion
Baseline to Week 24
Change in 400-Meter Walk Time
Time to walk 400 meters at the fastest pace possible
Baseline to Week 24
Change in Appendicular Lean Tissue Mass
Dual-energy x-ray absorptiometry (DXA) lean tissue mass in all four extremities
Baseline to Week 24
Change in Cross-Sectional Area of Trunk and Thigh Muscles
Computed tomography (CT) cross-sectional area of trunk and thigh muscles
Baseline to Week 24
Change in Frailty Phenotype
Fried Frailty Phenotype score, scored from 0 to 5 with higher indicating worse
Baseline to Week 24
Change in Quality of Life
36-Item Short Form Health Survey (SF-36), scored from 0 to 100 with higher indicating better
Baseline to Week 24
Change in Exercise Self-Efficacy
Exercise Self-Efficacy Scale, scored from 0 to 100 with higher indicating better
Baseline to Week 24
Change in Exercise Adherence
FitBit (step count heart rate time), exercise log (movement type, repetitions, load, rate of perceived exertion)
Baseline to Week 24
Change in Tissue Density of Trunk and Thigh Muscles
Computed tomography (CT) attenuation of trunk and thigh muscles
Baseline to Week 24
Change in Visceral Adipose Tissue Cross-Sectional Area
Computed tomography (CT) cross-sectional area at L4
Baseline to Week 24
معايير الأهلية

الأعمار المؤهلة للدراسة
بالغ, كبار السن
العمر الأدنى للدراسة
50 Years
الجنس المؤهل
الكل
  1. Men and women, 50-80 years old
  2. Documented HIV infection on suppressive antiretroviral therapy for at least 1 year with HIV-1 RNA <200 copies/mL and CD4+ T cell count >200/µL 3
  3. Sedentary lifestyle, defined as self-reported physical activity that breaks a sweat <3 days/week with no regular resistance exercise in the past 3 months
  4. ≥1 Fried frailty criterion (weakness, slow gait speed, exhaustion, decreased physical activity, or unintentional weight loss as defined by specific thresholds)
  5. Waist circumference ≥102 cm in men and ≥88 cm in women
  6. Normal mammogram within 2 years (females ≤74 years old) or prostate specific antigen <4 ng/mL (males ≤70 years old) per U.S. Preventive Services Task Force (USPSTF) age-appropriate cancer screening guidelines
  7. For females, postmenopausal defined as no menses for ≥12 months and anti-müllerian hormone (AMH) <20 pg/mL or history of bilateral oophorectomy at least 3 months ago
  8. Provider approval to participate

  1. Use of tesamorelin or other growth hormone (GH)-based therapy within 6 months
  2. Insulin-like growth factor 1 (IGF-1) z-score >2.0
  3. HbA1c >8%
  4. Active or suspected malignancy (with the exception of non-melanoma skin cancer) within 24 months
  5. Supraphysiologic testosterone or corticosteroid exposure, or change in exogenous testosterone or corticosteroid dose within 3 months
  6. Change in glucose-lowering medication (e.g., glucagon-like peptide-1 receptor agonists) within 3 months
  7. Active or unstable coronary artery disease, chest pain suspicious for angina, or serious arrythmia
  8. History of hypopituitarism, head irradiation, or other conditions known to affect the GH/IGF-1 axis
  9. Known hypersensitivity to tesamorelin or mannitol
  10. Acute or chronic illness judged by the investigator to represent a contraindication to study participation
Massachusetts General Hospital logoMassachusetts General Hospital
الجهة المسؤولة عن الدراسة
Lindsay Fourman, MD, المحقق الرئيسي, Assistant Professor of Medicine, Massachusetts General Hospital
جهة اتصال مركزية للدراسة
جهة اتصال: Lindsay T. Fourman, MD, 617-643-4590, [email protected]
جهة اتصال: Kristine M. Erlandson, MD, 303-724-4941, [email protected]
2 مواقع الدراسة في 1 بلدان

Colorado

University of Colorado - Anschutz Medical Campus, Aurora, Colorado, 80045, United States
Kristine M. Erlandson, MD, جهة اتصال, 303-724-4941, [email protected]
قيد التجنيد

Massachusetts

Massachusetts General Hospital, Boston, Massachusetts, 02114, United States
Lindsay T Fourman, MD, جهة اتصال, 617-643-4590, [email protected]
Julia Johnson, جهة اتصال, 617-724-5545, [email protected]
قيد التجنيد