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Resistance Training to Optimize Health in Pre-frail Older Adults

Resistance Training to Optimize Health in Pre-frail Older Adults

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02593084
Enrollment
36
Registered
2015-10-30
Start date
2016-01-31
Completion date
2017-09-30
Last updated
2018-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Frail Elderly

Keywords

Resistance Training, Exercise, Walking, Safety, Feasibility Studies

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

Interventions

BEHAVIORALHigher Intensity Resistance Training

Bi-weekly resistance training for 12 weeks using multi-joint movements involving both upper and lower extremities (e.g squats). Participants will perform 3-5 sets of 3-6 repetitions at Rating of Perceived Exertion 8/10. The intervention will be administered by a Physical Therapist or trained fitness professional.

BEHAVIORALLower Intensity Resistance Training

Bi-weekly resistance training for 12 weeks using single-joint movements involving both upper and lower extremities (e.g leg extension). Participants will perform 3-5 sets of 8-10 repetitions at Rating of Perceived Exertion 5/10. The intervention will be administered by a Physical Therapist or trained fitness professional.

Sponsors

Canadian Frailty Network
CollaboratorOTHER
McMaster University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* self-reported mobility limitations * living in the community * not currently engaged in regular resistance training * able to follow instructions

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

Design outcomes

Primary

MeasureTime frame
Occurrence of adverse eventsEntire duration of the intervention (12 weeks)
Attendance rateEntire duration of the intervention (12 weeks)
Attrition rateEntire duration of the intervention (12 weeks)

Secondary

MeasureTime frame
Activities-Specific Balance Confidence scale0, 12, 20 weeks
Muscle strength0, 12, 20 weeks
Short Form-360, 12, 20 weeks
Timed Up and Go Test0, 12, 20 weeks
Healthcare Utilization Questionnaires0, 12, 20 weeks
Peripheral Quantitative Computed Tomography analysis of muscle and bone quality0, 12, 20 weeks
EQ-5D-5L0, 12, 20 weeks
Caregiver Burden Interview Short Form0, 12, 20 weeks
Short Physical Performance Battery0, 12, 20 weeks
Berg Balance Scale0, 12, 20 weeks

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026