Resistance Training to Optimize Health in Pre-frail Older Adults
- Conditions
- Frail Elderly
- Interventions
- Behavioral: Higher Intensity Resistance TrainingBehavioral: Lower Intensity Resistance Training
- Registration Number
- NCT02593084
- Lead Sponsor
- McMaster University
- Brief Summary
Exercise programs, particularly resistance training programs using weights or resistance bands, can help improve or maintain mobility and function in older adults, preserve independent living, and improve quality of life. This study will examine the safety and feasibility of a novel, higher intensity resistance training program in older adults, and compare the effects with standard care, lower intensity training. It is anticipated that both programs will be safe and feasible, but higher-intensity training will lead to greater improvements in quality of life, mobility and strength, which are part of the physical phenotype definition of frailty and markers of mobility disability.
- Detailed Description
It is critically important to identify effective strategies to reduce the risk and impact of mobility disability and frailty in older adults. Exercise, particularly resistance training (RT), has the potential to influence a person's ability to navigate around their environment and impact the components of the frailty phenotype which include weakness, physical inactivity, and slowness. Higher training intensities have been used with athletes and younger adults to achieve greater gains in strength, but the feasibility and effectiveness is less established in older persons who exhibit preclinical disability, or are at-risk for mobility decline where conservative protocols are typically employed. Higher intensity RT may be an innovative and effective strategy in preclinical disability pre-frailty to reduce the risk and impact of future frailty and mobility decline.
This study aims to examine: 1) the safety and feasibility of a 12-week higher intensity RT protocol in community dwelling older adults at risk for mobility disability, and 2) the effects of this protocol on walking, balance, muscle strength, quality of life compared to lower intensity RT
It is hypothesized that the higher intensity RT: 1) is safe and feasible for at-risk community-dwelling older adults, 2) more effective in improving walking, balance, muscle strength, and quality of life than lower intensity RT
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 36
- self-reported mobility limitations
- living in the community
- not currently engaged in regular resistance training
- able to follow instructions
- contraindications for intensive resistance training (e.g. recent cardiovascular event, fracture within the past 12 months)
- musculoskeletal injuries for which intervention participants are receiving concomitant rehabilitation treatments
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Higher Intensity Resistance Training Higher Intensity Resistance Training Participants will take part in a 12-week higher-intensity resistance training protocol. Lower Intensity Resistance Training Lower Intensity Resistance Training Participants will take part in a 12-week lower-intensity resistance training protocol that will serve as the active comparator.
- Primary Outcome Measures
Name Time Method Attendance rate Entire duration of the intervention (12 weeks) Attrition rate Entire duration of the intervention (12 weeks) Occurrence of adverse events Entire duration of the intervention (12 weeks)
- Secondary Outcome Measures
Name Time Method Short Physical Performance Battery 0, 12, 20 weeks Activities-Specific Balance Confidence scale 0, 12, 20 weeks Healthcare Utilization Questionnaires 0, 12, 20 weeks EQ-5D-5L 0, 12, 20 weeks Short Form-36 0, 12, 20 weeks Timed Up and Go Test 0, 12, 20 weeks Berg Balance Scale 0, 12, 20 weeks Muscle strength 0, 12, 20 weeks Peripheral Quantitative Computed Tomography analysis of muscle and bone quality 0, 12, 20 weeks Caregiver Burden Interview Short Form 0, 12, 20 weeks
Trial Locations
- Locations (1)
McMaster University
🇨🇦Hamilton, Ontario, Canada