Moderate Intensity vs High Intensity Interval Training in Women With Heart Failure
2026年6月17日 更新者：Riphah International University
Effects of Moderate Intensity Exercise vs High Intensity Interval Training on Functional Capacity and Quality of Life in Women With Heart Failure
- To determine the effects of moderate intensity exercise vs high intensity interval training on functional capacity in women with heart failure
- To determine the effects of moderate intensity exercise vs high intensity interval training on quality of life in women with heart failure
研究概览
研究类型
介入性
注册 (估计的)
64
阶段
- 不适用
联系人和位置
本节提供了进行研究的人员的详细联系信息，以及有关进行该研究的地点的信息。
学习联系方式
- 姓名：Muhammad Iqbal Tariq
- 电话号码：333826752
- 邮箱：iqbal.tariq@riphah.edu.pk
学习地点
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Fedral
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Islamabad、Fedral、巴基斯坦、44000
- Riphah International University
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接触：
- Dua Yasin, MSPT*
- 电话号码：+92 318 5084334
- 邮箱：duayasin7@gmail.com
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首席研究员：
- Dua Yasin, MSPT*
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参与标准
研究人员寻找符合特定描述的人，称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
不
描述
Inclusion Criteria:
- Women aged 40-70 years, diagnosed with Stable Heart Failure (NYHA class II or III).
- Clinically stable patients referred for exercise-based cardiac rehabilitation by the physician.
- Able to perform exercise testing (able to walk 150 meters on the six-minute walk test) before starting the program.
- Women willing to participate and provide informed consent.
Exclusion Criteria:
- Unstable Heart failure or myocardial infarction (< 4 weeks).
- Severe arrhythmias, uncontrolled hypertension, or ongoing chest pain during exercise.
- Orthopedic, neurological, or cognitive limitations preventing safe exercise participation.
- Any medical contraindication to exercise testing.
- Refusal or inability to provide informed consent or comply with the rehabilitation program.
学习计划
本节提供研究计划的详细信息，包括研究的设计方式和研究的衡量标准。
研究是如何设计的？
设计细节
- 主要用途：治疗
- 分配：随机化
- 介入模型：并行分配
- 屏蔽：无（打开标签）
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的：高强度间歇训练
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Group B will perform a high-intensity interval training (HIIT) program designed according to established cardiac rehabilitation protocols.
Bicycle ergometer will be used, in which each session will begin with a 10-minute warm-up (lower limb large muscle stretches), followed by intervals performed at 80% of heart rate reserve (HRR) for 3 min, alternating with recovery periods at low intensity 40% of HRR for 3 min.
The total exercise duration will be approximately 30 minutes per session, conducted three times weekly for 12 weeks under supervision.
Participants will be encouraged to maintain self-directed exercise after the intervention period
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有源比较器：moderate-intensity aerobic training
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Group A will undergo a moderate-intensity aerobic training program as part of a structured cardiac rehabilitation protocol.
The program will be supervised sessions, conducted three times per week for 12 weeks.
Each session will include approximately 30 minutes of aerobic exercise performed on a bicycle ergometer at an intensity of 60% of heart rate reserve (HRR)
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研究衡量的是什么？
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Six-minute walk test
大体时间：Baseline and 12 Week
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The Six-Minute Walk Test (6MWT) is a simple, submaximal test that evaluates functional capacity and exercise capacity in patients with chronic heart failure by measuring the distance walked and estimating peak VO2.
It will be performed in a 30-meter corridor, where participants will walk as far as possible in six minutes, with heart rate and oxygen saturation monitored before and after the test.
This study tested the validity and reliability of the six-minute walk test (6MWT) in cardiac rehabilitation patients, including those with heart failure.
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Baseline and 12 Week
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EuroQol 5-Dimension Questionnaire
大体时间：Baseline and 12 week
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EuroQol 5-Dimension Questionnaire (EQ-5D): The EuroQol-5 Dimension (EQ-5D) is a questionnaire used to measure quality of life (QoL).
It evaluates five key areas: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression.
Each area has one question, and responses together describe a person's overall health status.
For the 5L, scores range from 5 to 25.
A lower score indicates better health, while a higher score indicates greater health problems.
Patients rate their overall health TODAY on a vertical scale from 0 (worst imaginable health) to 100 (best imaginable health)
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Baseline and 12 week
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
调查人员
- 首席研究员：Muhammad iqbal Tariq, PhD*、Riphah International University
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查，以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (估计的)
2026年7月1日
初级完成 (估计的)
2026年12月1日
研究完成 (估计的)
2026年12月1日
研究注册日期
首次提交
2026年6月17日
首先提交符合 QC 标准的
2026年6月17日
首次发布 (实际的)
2026年6月23日
研究记录更新
最后更新发布 (实际的)
2026年6月23日
上次提交的符合 QC 标准的更新
2026年6月17日
最后验证
2026年6月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索，没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求，请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改，我们的网站上也会自动更新.