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Resistance Training to Optimize Health in Pre-frail Older Adults

Not Applicable
Completed
Conditions
Frail Elderly
Interventions
Behavioral: Higher Intensity Resistance Training
Behavioral: 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
Inclusion Criteria
  • self-reported mobility limitations
  • living in the community
  • not currently engaged in regular resistance training
  • able to follow instructions
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Exclusion Criteria
  • 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
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Higher Intensity Resistance TrainingHigher Intensity Resistance TrainingParticipants will take part in a 12-week higher-intensity resistance training protocol.
Lower Intensity Resistance TrainingLower Intensity Resistance TrainingParticipants will take part in a 12-week lower-intensity resistance training protocol that will serve as the active comparator.
Primary Outcome Measures
NameTimeMethod
Attendance rateEntire duration of the intervention (12 weeks)
Attrition rateEntire duration of the intervention (12 weeks)
Occurrence of adverse eventsEntire duration of the intervention (12 weeks)
Secondary Outcome Measures
NameTimeMethod
Short Physical Performance Battery0, 12, 20 weeks
Activities-Specific Balance Confidence scale0, 12, 20 weeks
Healthcare Utilization Questionnaires0, 12, 20 weeks
EQ-5D-5L0, 12, 20 weeks
Short Form-360, 12, 20 weeks
Timed Up and Go Test0, 12, 20 weeks
Berg Balance Scale0, 12, 20 weeks
Muscle strength0, 12, 20 weeks
Peripheral Quantitative Computed Tomography analysis of muscle and bone quality0, 12, 20 weeks
Caregiver Burden Interview Short Form0, 12, 20 weeks

Trial Locations

Locations (1)

McMaster University

🇨🇦

Hamilton, Ontario, Canada

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