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临床试验/NCT04653350
NCT04653350已完成不适用

Effects of High Intensity Multi-Modal Exercise Training on Bone Density and Functional Performance in Postmenopausal Women

Riphah International University2 个研究点 分布在 1 个国家目标入组 58 人开始时间: 2020年11月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
58
试验地点
2
主要终点
Femoral Neck BMD (FN BMD)

研究概览

简要总结

in Pakistan 9.9 million people are osteoporotic and 7.2 million amongst them are women. Globally after every 3 seconds there is occurrence of fragility fracture.In Pakistan females carries different risk factors based on distinct culture, environment, diet and lifestyle. So there is dire need to conduct more high quality clinical trials at National level in order to establish strong evidence in favor of low cost but highly effective exercise protocols for such a significant public health issue.

详细描述

In postmenopausal age, women bones get weak and easily fracture after 50years. In Pakistan every other female is silently suffering from this disease leading to bone, joint pain and disability. This project is innovatively designed first time in Pakistan to target weak bones of women with high intensity, progressive exercise training. The objectives of this study are to determine the effects of a high intensity multi-modal exercise training on bone mineral density and functional performance in postmenopausal women.

After initial screening based on history, subjective fracture risk calculations and subjective osteoporosis screening. Females fulfilling criteria and willing to participate in exercise trial will be recruited in the study. At baseline, DEXA scan will be done for Femoral and lumbar bone density. All performance based testing for functional performance outcome measures would be done at baseline, after 3 months & after 6 months. Patient will be called twice a week for 8months and DEXA will be repeated after 8months of training. It is hypothesized that supervised exercise training will improve bone mineral density and functional performance in postmenopausal women with low bone mass.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

盲法说明

Females participating in a clinical trial will be kept blind with respect to their allocated exercise group. The assessor doing reporting for the DEXA scan will also be kept blind about the patient group.

入排标准

年龄范围
45 Years 至 70 Years(Adult, Older Adult)
性别
Female
接受健康志愿者
是

入选标准

  • •Postmenopausal Women, at least 3 years since last mensuration.
  • •Age: 45-70years
  • •Body mass index (BMI) <30kg/m2
  • •Community ambulant without walking aid
  • •Good general health
  • •Willing for exercise therapy

排除标准

  • •History of fragility fracture in addition to BMD T-score of -2.5 or less
  • •MMSE < 20
  • •Taking Hormone replacement therapy or steroids from last 1 year.
  • •Had participated in regular exercise for last 1 year
  • •Systemic illness: hyperthyroidism, hyperparathyroidism, Diabetes Mellitus, renal failure, any malignancy, extensive radiation exposure
  • •Any orthopedic injury/disorder hindering performance of exercise.

研究组 & 干预措施

HIT-MMEX Group

Experimental

In this group Supervised High intensity Progressive Resistance Training, High intensity weightbearing/Impact exercises and High challenging Balance Training will be given. 2 times/week for 40-50minutes session progressively over the duration of 8 months.

干预措施: High Intensity Exercises (Other)

Control Group

Active Comparator

In this Group Supervised general fitness exercises including general body stretches, treadmill walking, mild to moderate intensity progressive resistance training & balance exercises will be given. 2 times/week for 40-50minutes session progressively over the duration of 8 months.

干预措施: General Exercises (Other)

结局指标

主要结局

Femoral Neck BMD (FN BMD)

时间窗: 8 Months

Change from Baseline in Femoral Neck Bone Mineral Density measured by DEXA scan

Lumbar Spine BMD (LS BMD)

时间窗: 8 Months

Change from Baseline in Lumbar Spine Bone Mineral Density measured by DEXA scan

次要结局

  • 30-second sit to stand test (Reps)(6 Months)
  • Berg balance scale(6 Months)
  • Time up and Go test(6 Months)
  • Dynamic Gait Index(6 Months)
  • 1 RM for Trunk Extensors(6 Months)
  • Functional Reach Test (FRT)(6 Months)
  • 1 RM for Leg Extensors(6 Months)
  • Falls Efficacy Scale(6 Months)
  • 1 RM for Leg Extensors(3 Months)
  • 1 RM for Trunk Extensors(3 Months)
  • 30-second sit to stand test (Reps)(3 Months)
  • Time up and Go test(3 Months)
  • Dynamic Gait Index(3 Months)
  • Falls Efficacy Scale(3 Months)
  • Berg balance scale(3 Months)
  • Functional Reach Test (FRT)(3 Months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Huma Riaz

Associate Professor

Riphah International University

研究点 (2)

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