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临床试验/NCT00462722
NCT00462722已完成不适用

COX Inhibition & Musculoskeletal Responses to Exercise

University of Colorado, Denver1 个研究点 分布在 1 个国家目标入组 159 人开始时间: 2007年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
159
试验地点
1
主要终点
Percentage Change From Baseline in Lumbar Spine Bone Mineral Density (BMD) at 9 Months

研究概览

简要总结

The purpose of this study is to determine if the use of ibuprofen blocks the benefits of exercise to build bone and muscle mass.

详细描述

People are advised to engage in weight-bearing physical activity to help prevent the loss of bone and muscle mass that occurs with aging. There is evidence from studies of animals that non-steroidal anti-inflammatory drugs (NSAIDS), such as ibuprofen, block some of the bone- and muscle-building effects of exercise. The aim of this study is to determine whether use of ibuprofen, either before or after exercise, blocks the benefits of exercise training on bone and skeletal muscle in older women and men. The hypothesis is that taking ibuprofen before exercise will block some of the effects of exercise training to increase bone density and muscle mass.

Women and men aged 60-75 years will complete a supervised, 9-month exercise training program designed to increase bone and muscle mass. The training will include weight lifting and weight-bearing exercises, such as jumping in place and treadmill walking, up to 5 days per week. Participants will be randomly assigned to take 1 of 3 study pill combinations before and after each exercise session. The combinations of study pills will be: placebo before/placebo after, placebo before/ibuprofen after, or ibuprofen before/placebo after. The dose of ibuprofen will be 400 mg. Bone density of the hip and spine, body composition (total body muscle and fat), and markers of bone turnover in the blood will be measured before and after 4.5 and 9 months of training. Muscle cross-sectional area of the thigh will be measured by CT before and after 9 months of training. A subset of participants will have biopsies of the thigh muscle before and after training to measure proteins and genes associated with muscle build-up and breakdown.

Volunteers who do not use ibuprofen, aspirin, or acetaminophen more than 3 days per month will be enrolled. People with intolerance to ibuprofen or related drugs, cardiovascular disease, or orthopedic problems that limit exercise will be excluded from the study.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
60 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Aged 60 to 75 years
  • Willing to participate in a 9-month supervised exercise program that will start at a moderate intensity and gradually progress to a vigorous intensity
  • Not currently performing regular, moderate-to-vigorous weight-bearing or weight-lifting exercise
  • Average use of NSAIDs (including low-dose aspirin) or acetaminophen less than 3 days per month

排除标准

  • Relative or absolute contraindications to regular use of NSAIDs
  • Known allergy or intolerance (heartburn, stomach pain, nausea, vomiting) to NSAIDs; controlled GERD(Gastroesophageal Reflux Disease), if not related to NSAID use, will not be an exclusion criterion
  • Proton Pump Inhibitor (PPI) use if dose is unstable or if using for less than 6 months prior to study enrollment
  • History of peptic ulcer or upper GI bleeding
  • Asthma with bronchospasm induced by aspirin or other NSAIDs
  • Moderate or severe renal impairment defined as a calculated creatinine clearance
  • Chronic hepatobiliary disease, conservatively defined as liver function tests greater than 1.5 times the upper limit of normal (if such values are obtained on initial screening and thought to be transient in nature, repeated testing will be allowed)
  • Hyperkalemia
  • Osteoporosis
  • Diabetes mellitus requiring pharmacologic therapy
  • Congestive heart failure
  • Uncontrolled hypertension; use of thiazide diuretics will be allowed if on a stable dose for at least 6 months
  • Cardiovascular disease
  • Thyroid dysfunction
  • Orthopedic problems (e.g., chronic back pain, severe osteoarthritis, rheumatoid arthritis) that limit the ability to perform vigorous exercise and increase the likelihood that the volunteer will use pain medications other than the study pills
  • Certain use of medications, including
  • Drugs that are known to alter bone metabolism (e.g., estrogen, SERMs(Selective estrogen-receptor modulators), testosterone, bisphosphonates, teriparatide, calcitonin, GnRH(Gonadotropin-releasing hormone) agonists)
  • Chronic use of oral corticosteroids or any use in the previous 6 months (use of inhaled steroids will not be an exclusion criterion based on a meta-analysis documenting that the effect on bone is not significant)
  • Average use of acetaminophen or NSAIDs, including low-dose aspirin, greater than 3 days per month; volunteers using aspirin for primary prevention may enroll in the study if they discontinue aspirin therapy for the 9-month intervention period
  • Anticoagulants (e.g., warfarin, clopidogrel)
  • Narcotics

研究组 & 干预措施

Ibuprofen pre and placebo post exercise

Experimental

ibuprofen before and placebo after musculoskeletal-loading exercise

干预措施: Ibuprofen (Drug)

Placebo pre and post exercise

Placebo Comparator

placebo before and after musculoskeletal-loading exercise

干预措施: Placebo (Drug)

Placebo pre and post exercise

Placebo Comparator

placebo before and after musculoskeletal-loading exercise

干预措施: musculoskeletal-loading exercise (Behavioral)

Placebo pre and ibuprofen post exercise

Experimental

placebo before and ibuprofen after musculoskeletal-loading exercise

干预措施: Ibuprofen (Drug)

Placebo pre and ibuprofen post exercise

Experimental

placebo before and ibuprofen after musculoskeletal-loading exercise

干预措施: Placebo (Drug)

Placebo pre and ibuprofen post exercise

Experimental

placebo before and ibuprofen after musculoskeletal-loading exercise

干预措施: musculoskeletal-loading exercise (Behavioral)

Ibuprofen pre and placebo post exercise

Experimental

ibuprofen before and placebo after musculoskeletal-loading exercise

干预措施: Placebo (Drug)

Ibuprofen pre and placebo post exercise

Experimental

ibuprofen before and placebo after musculoskeletal-loading exercise

干预措施: musculoskeletal-loading exercise (Behavioral)

结局指标

主要结局

Percentage Change From Baseline in Lumbar Spine Bone Mineral Density (BMD) at 9 Months

时间窗: Baseline and after 9 months of training

Percentage Change From Baseline in Total Hip Bone Mineral Density (BMD) at 9 Months

时间窗: Baseline and after 9 months of training

Change From Baseline in Fat-free Mass at 9 Months

时间窗: Baseline and after 9 months of training

次要结局

  • Percentage Change From Baseline in Femoral Neck Bone Mineral Density (BMD) at 9 Months(Baseline and after 9 months of training)
  • Percentage Change From Baseline in Trochanter Bone Mineral Density (BMD) at 9 Months(Baseline and after 9 months of training)
  • Percentage Change From Baseline in Sub-trochanter Bone Mineral Density (BMD) at 9 Months(Baseline and after 9 months of training)
  • Change in Thigh Cross-sectional Muscle Area(Baseline and after 9 months of training)
  • Bone Turnover Markers(Baseline, and after 4.5 & 9 months of training)
  • Expression of Selected Proteins and Genes Associated With Muscle Build-up and Breakdown(Baseline and after 9 months of training)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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