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临床试验/NCT07660653
NCT07660653已完成不适用

Effect of Resistance-Led Multicomponent Training Combined With Nutritional Supplementation on Intrinsic Capacity and Disability Risk in Chinese Rural Older Adults

Capital University of Physical Education and Sports, China1 个研究点 分布在 1 个国家目标入组 220 人开始时间: 2025年6月18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
发起方
入组人数
220
试验地点
1
主要终点
Change From Baseline in Short Physical Performance Battery Score at Week 12

研究概览

简要总结

This study is a five-arm, parallel-group, assessor-blinded randomized controlled trial designed to evaluate the effects of resistance-dominant multicomponent training combined with nutritional supplementation on intrinsic capacity and disability risk among rural Chinese older adults. A total of 220 participants aged 60 years or older with mobility decline, nutritional risk, sarcopenia risk, or pre-frailty/frailty will be randomly assigned to one of five groups: control, nutrition supplementation alone, resistance training alone, resistance training plus nutrition supplementation, or resistance-dominant multicomponent training plus nutrition supplementation. The intervention will last 12 weeks. Exercise interventions will be conducted three times per week, and nutritional supplementation will include leucine-enriched whey protein and vitamin D. The primary outcomes are the Short Physical Performance Battery score, FRAIL score, and activities of daily living/instrumental activities of daily living scores. Secondary outcomes include gait speed, Timed Up and Go test, sit-to-stand performance, handgrip strength, nutritional status, protein intake, serum 25-hydroxyvitamin D, calf circumference, and appendicular skeletal muscle mass index.

详细描述

This study aims to determine whether resistance-dominant multicomponent training combined with leucine-enriched whey protein and vitamin D supplementation can improve intrinsic capacity and reduce disability risk in rural Chinese older adults. The study focuses on the locomotion and vitality domains of intrinsic capacity, which are closely related to mobility function, nutritional status, muscle reserves, and the ability to maintain independent daily living.

Eligible participants will be rural community-dwelling adults aged 60 years or older who present at least one of the following risk characteristics: reduced physical performance, low gait speed, nutritional risk, sarcopenia risk, or pre-frailty/frailty. After baseline assessment, participants will be randomly allocated in a 1:1:1:1:1 ratio to one of five study groups: control group, nutrition supplementation group, resistance training group, resistance training plus nutrition supplementation group, and resistance-dominant multicomponent training plus nutrition supplementation group.

The traditional resistance training program will include progressive functional resistance exercises such as chair sit-to-stand, chair-assisted squat, calf raise, elastic-band knee extension, elastic-band hip abduction, elastic-band rowing, wall push-up, and shoulder press. The resistance-dominant multicomponent training program will use resistance training as the core component and will additionally include balance, gait, aerobic, flexibility, and breathing relaxation exercises. Exercise sessions will be conducted three times per week for 12 weeks.

The nutritional supplementation will consist of approximately 20 g/day whey protein, 2.5-3.0 g/day total leucine, and 800-1000 IU/day vitamin D3. The supplement will be administered twice daily. On training days, one dose will be taken within 30 minutes to 2 hours after exercise, and another dose after breakfast. On non-training days, the supplement will be taken after breakfast and dinner.

Outcome assessments will be performed at baseline and at week 12. The primary outcomes are the Short Physical Performance Battery score, FRAIL score, and activities of daily living/instrumental activities of daily living scores. Secondary outcomes include 4-meter gait speed, Timed Up and Go test, five-times sit-to-stand test, 30-second chair stand test, handgrip strength, Mini Nutritional Assessment Short Form score, daily protein intake, serum 25-hydroxyvitamin D, body mass index, calf circumference, appendicular skeletal muscle mass index, and quality of life. Safety outcomes include renal function, blood calcium, falls, musculoskeletal injury, gastrointestinal symptoms, and other adverse events.

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
Single (Outcomes Assessor)

盲法说明

Due to the nature of the exercise intervention, participants and exercise instructors cannot be fully blinded to exercise allocation. Outcome assessors will be blinded to group assignment. For the nutritional supplementation component, the active supplement and the isocaloric placebo will be similar in appearance, taste, packaging, and administration frequency.

入排标准

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

入选标准

  • Aged 60 years or older.
  • Rural residents who have lived in the study area for at least 6 months and have no plan for long-term absence during the study period.
  • Able to walk independently or with a cane for a short distance.
  • Meeting at least one of the following risk characteristics: Short Physical Performance Battery score of 9 or lower, usual gait speed of 0.8 m/s or lower, Mini Nutritional Assessment Short Form score of 11 or lower, SARC-F score of 4 or higher, possible sarcopenia according to the Asian Working Group for Sarcopenia 2019 criteria, or FRAIL score of 1 to
  • Able to understand the study requirements and provide written informed consent.

排除标准

  • Unstable cardiovascular or cerebrovascular events within the past 6 months.
  • Severe uncontrolled hypertension, defined as resting systolic blood pressure of 180 mmHg or higher or diastolic blood pressure of 110 mmHg or higher.
  • Severe cognitive impairment that prevents understanding of or cooperation with the study procedures.
  • Severe osteoarticular disease or neurological disease affecting exercise safety.
  • Severe renal dysfunction, such as estimated glomerular filtration rate lower than 30 mL/min/1.73 m², or considered unsuitable for protein supplementation by the study physician.
  • Hypercalcemia, active kidney stones, or contraindications to vitamin D supplementation.
  • Allergy to whey protein or any component of the nutritional supplement.
  • Regular use of protein powder, beta-hydroxy-beta-methylbutyrate, creatine, or other nutritional supplements that may affect muscle metabolism within the past 3 months.
  • Participation in another interventional study.

研究组 & 干预措施

Control Group

Placebo Comparator

Participants in this group will receive routine health education and an isocaloric placebo without structured exercise training for 12 weeks.

干预措施: Routine Health Education (Behavioral)

Control Group

Placebo Comparator

Participants in this group will receive routine health education and an isocaloric placebo without structured exercise training for 12 weeks.

干预措施: Isocaloric Placebo (Dietary Supplement)

Nutrition Supplementation Group

Experimental

Participants in this group will receive leucine-enriched whey protein and vitamin D supplementation without structured exercise training for 12 weeks.

干预措施: Leucine-Enriched Whey Protein and Vitamin D Supplementation (Dietary Supplement)

Resistance Training Group

Experimental

Participants in this group will receive supervised progressive resistance training three times per week for 12 weeks and an isocaloric placebo.

干预措施: Isocaloric Placebo (Dietary Supplement)

Resistance Training Group

Experimental

Participants in this group will receive supervised progressive resistance training three times per week for 12 weeks and an isocaloric placebo.

干预措施: Progressive Resistance Training (Behavioral)

Resistance Training Plus Nutrition Group

Experimental

Participants in this group will receive supervised progressive resistance training three times per week for 12 weeks combined with leucine-enriched whey protein and vitamin D supplementation.

干预措施: Leucine-Enriched Whey Protein and Vitamin D Supplementation (Dietary Supplement)

Resistance Training Plus Nutrition Group

Experimental

Participants in this group will receive supervised progressive resistance training three times per week for 12 weeks combined with leucine-enriched whey protein and vitamin D supplementation.

干预措施: Progressive Resistance Training (Behavioral)

Resistance-Dominant Multicomponent Training Plus Nutrition Group

Experimental

Participants in this group will receive supervised resistance-dominant multicomponent training three times per week for 12 weeks combined with leucine-enriched whey protein and vitamin D supplementation.

干预措施: Leucine-Enriched Whey Protein and Vitamin D Supplementation (Dietary Supplement)

Resistance-Dominant Multicomponent Training Plus Nutrition Group

Experimental

Participants in this group will receive supervised resistance-dominant multicomponent training three times per week for 12 weeks combined with leucine-enriched whey protein and vitamin D supplementation.

干预措施: Resistance-Dominant Multicomponent Training (Behavioral)

结局指标

主要结局

Change From Baseline in Short Physical Performance Battery Score at Week 12

时间窗: Baseline and Week 12

The Short Physical Performance Battery will be used to assess lower-extremity physical performance, including standing balance, 4-meter gait speed, and five-times sit-to-stand performance. Total scores range from 0 to 12, with higher scores indicating better physical performance.

Change From Baseline in FRAIL Score at Week 12

时间窗: Baseline and Week 12

The FRAIL scale will be used to assess frailty status. The scale includes fatigue, resistance, ambulation, illness, and loss of weight. Scores range from 0 to 5, with higher scores indicating greater frailty risk.

Change From Baseline in Activities of Daily Living Score at Week 12

时间窗: Baseline and Week 12

Activities of daily living will be assessed to evaluate basic self-care ability in daily life. Higher scores indicate better basic daily living function.

Change From Baseline in Instrumental Activities of Daily Living Score at Week 12

时间窗: Baseline and Week 12

Instrumental activities of daily living will be assessed to evaluate more complex daily living abilities. Higher scores indicate better instrumental daily living function.

次要结局

未报告次要终点

研究者

发起方
Capital University of Physical Education and Sports, China
申办方类型
Other
责任方
Principal Investigator
主要研究者

Yongzhao Fan

Associate Professor

Capital University of Physical Education and Sports, China

研究点 (1)

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