跳至主要内容
临床试验/NCT06107855
NCT06107855已完成不适用

Comparison of Low-dose Maximal-intent Versus Controlled-tempo Resistance Training on Quality-of-life, Functional Capacity, and Strength in Untrained Healthy Adults: a Randomised Controlled Trial

Northumbria University1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2022年8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
20
试验地点
1
主要终点
Quality-of-life

研究概览

简要总结

The aims of this study were to:

  1. Compare the effects of low-dose Maximal Intent and Controlled Tempo Resistance Training on untrained healthy adults' quality-of-life, functional capacity, and strength.
  2. Qualitatively explore perceptions of Maximal Intent and Controlled Tempo Resistance Training.

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
None

入排标准

年龄范围
30 Years 至 59 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Participants were eligible if they were between 30-60 years old
  • •Uninjured
  • •Had no cardiovascular or neuromuscular conditions
  • •Had not participated in lower-limb RT in the previous six months.

排除标准

  • •Participants were excluded if they had either taken part in any lower-limb RT in the last six months
  • •Had underlying health condition(s) that prevented them from participating in RT
  • •Regularly met or exceeded the UK recommended PA guideline of 150-minutes of moderate to intense PA per week.

研究组 & 干预措施

Maximal-intent Resistance Training

Experimental

The MI group was instructed and encouraged to deliberately commit to exerting maximal effort and force during the concentric phase of the leg press with the intention of achieving the greatest velocity possible.

干预措施: Leg Press Resistance Training Machine (Other)

Controlled-tempo Resistance Training

Experimental

While the CT group followed the metronome for both eccentric and concentric phases.

干预措施: Leg Press Resistance Training Machine (Other)

结局指标

主要结局

Quality-of-life

时间窗: The time frame for my testing intervals will be conducted at specific time points: at baseline, Week 1, Week 4, and Week 9, out of a total study duration of 9 weeks.

Participant quality of life (focus group questions \& SF-36)

次要结局

  • Strength (1RM)(The time frame for my testing intervals will be conducted at specific time points: at baseline, Week 1, Week 4, and Week 9, out of a total study duration of 9 weeks.)
  • Timed-up-and-go (TUG)(The time frame for my testing intervals will be conducted at specific time points: at baseline, Week 1, Week 4, and Week 9, out of a total study duration of 9 weeks.)
  • 30-second sit-to-stand (30s-STS)(The time frame for my testing intervals will be conducted at specific time points: at baseline, Week 1, Week 4, and Week 9, out of a total study duration of 9 weeks.)
  • BMI(The time frame for my testing intervals will be conducted at specific time points: at baseline, Week 1, Week 4, and Week 9, out of a total study duration of 9 weeks.)
  • Balance(The time frame for my testing intervals will be conducted at specific time points: at baseline, Week 1, Week 4, and Week 9, out of a total study duration of 9 weeks.)
  • 6-minute Walk Test (6MWT)(The time frame for my testing intervals will be conducted at specific time points: at baseline, Week 1, Week 4, and Week 9, out of a total study duration of 9 weeks.)
  • Strength-to-mass(The time frame for my testing intervals will be conducted at specific time points: at baseline, Week 1, Week 4, and Week 9, out of a total study duration of 9 weeks.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验