跳至主要内容
临床试验/NCT06825130
NCT06825130招募中不适用

Feasibility and Preliminary Efficacy of High-intensity Interval Training Combined with Muscle-strength Training in Older Women: Pilot Randomized Controlled Trial

University of Nottingham1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2025年2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
招募中
入组人数
20
试验地点
1
主要终点
Feasibility of high-intensity interval training combined with muscle strength training

研究概览

简要总结

Women generally live longer than men but often experience a faster muscle mass loss due to inactivity, which can lead to weakness and disability. Despite these risks, women, particularly older women, are less active than men. In England, less than one-third of women engage in sufficient aerobic activity, and less than 5% do enough muscle strength training. Common reasons for not exercising include lack of time and enjoyment.

High-intensity interval training (HIIT) is an efficient and effective way to exercise that many women find more enjoyable than longer workouts. HIIT has been shown to be effective in older women, helping them improve their fitness with less time commitment. Because HIIT is time-efficient, it can be combined with muscle strength training without significantly increasing the duration of the exercise session, which may lead to even better fitness results.

This study will assess how practical it is for older women to do HIIT and strength exercise combined training. It will also investigate whether this combined approach can improve overall fitness, muscle strength, aerobic fitness, and quality of life more than HIIT alone.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

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

入选标准

  • •Females (biologically at birth)
  • •At least 60 years of age at the time of signing the informed consent
  • •Non-smoker, including electronic cigarettes
  • •Not participating in routine high-intensity aerobic or muscle strength exercise training (≥ 75 min/week of structured vigorous aerobic exercise, or 2 times /week of structured muscle strength training)
  • •Able to perform a cardiopulmonary exercise testing (CPET) to exhaustion
  • •willing to complete baseline and follow-up measures, and attend prescribed exercise sessions at the University of Nottingham
  • •willing and able to give informed consent for participation in the study

排除标准

  • •Diagnosed with cardiovascular disease, kidney disease, diabetes, obstructive pulmonary disease, or uncontrolled hypertension
  • •History or current neurological or psychiatric illness, or motor or cognitive restrictions
  • •Contraindications to symptom-limited cardiopulmonary exercise testing (CPET), including resting hypertension with systolic blood pressure >200 mmHg or diastolic blood pressure > 110 mmHg, uncorrected medical conditions, such as significant anemia, important electrolyte imbalance, and hyperthyroidism, mental impairment with limited ability to cooperate, physical disability that precludes safe and adequate testing.
  • •Having taken part in a research study in the last 3 months involving invasive procedures or an inconvenience allowance.

研究组 & 干预措施

aerobic training + muscle strength training

Experimental

3 days/week -- 3-min warm up at 60% of HR@VT2 on a bike ergometer -- 6 x 1-min machine-base muscle strength exercises: leg press, chest press, knee extension, lat pull down, knee flexion, and shoulder raise -- 6 x 1-min high-intensity interval bouts at 80% HR@VT2 interspersed by 1-min active recovery will be performed.

干预措施: Exercise (Behavioral)

aerobic training

Active Comparator

3 days/week -- 3-min warm up at 60% of HR@VT2 on a bike ergometer -- 2 blocks of 6 x 1-min high-intensity interval bouts at 70% HR@VT2 interspersed by 1-min active recovery

干预措施: Exercise (Behavioral)

结局指标

主要结局

Feasibility of high-intensity interval training combined with muscle strength training

时间窗: From recruitment to week-12

will be assessed from recruitment, adherence, compliance, safety, subjective exercise experiences and self-efficacy. Recruitment will be assessed by the proportion of patients remained interested and randomized after being informed of the requirements of the study; adherence will be assessed by the attendance to the prescribed exercise sessions; and compliance will be assessed by the proportion of participants adhering to prescribed exercise intensity. For safety, all mild, moderate, and severe symptoms and adverse events throughout this study will be recorded.

次要结局

  • functional capacity(From baseline to week-12)
  • muscle function(From baseline to week-12)
  • cardiorespiratory fitness(From baseline to week-12)
  • muscle mass(From baseline to week-12)
  • QoL(From baseline to week-12)

研究者

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

Tasuku Terada

Dr

University of Nottingham

研究点 (1)

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