The Effect of Walking on Frailty

Sponsor
Northwestern University (Other)
Overall Status
Recruiting
CT.gov ID
NCT03654807
Collaborator
(none)
200
1
2
54.1
3.7

Study Details

Study Description

Brief Summary

The purpose of this study is to test the effect of walking intensity on both frailty category (i.e., frail, pre-frail, and nonfrail) and frailty score as a continuous outcome on the SHARE-FI (frailty instrument). As well as test the effect of walking intensity on mobility, physical function, balance, and total Physical Activity.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: High Intensity Walking
  • Behavioral: Casual Speed Walking
N/A

Detailed Description

Frailty impacts up to 60% of older adults and is a leading cause of dependency among older adults. Frail older adults experience physical problems such as balance difficulties, weakness, decreased endurance, and reduced walking speed that increase risk for falls, hospitalizations, institutionalization, and death. Physical activity has multi-system health benefits and is the most recommended frailty management intervention, but guidelines regarding the specific intensity of physical activity remain unclear. High intensity physical activity is an established and safe therapeutic approach in other populations, but it is unclear as to the extent to which high intensity activity can reduce or reverse frailty. This cluster-randomized study will compare a high intensity walking (HIW) intervention to a self-selected, casual speed walking (CSW) intervention implemented within retirement communities for pre-frail and frail older adults. Investigators will randomize 10 retirement communities with 20 participants at each site (200 total participants) to either a 4-month HIW or CSW intervention. All participants will receive 48, individually supervised overground walking sessions occurring within their retirement community. At the beginning and end of the study, investigators will measure participants' frailty, mobility, physical functioning, balance, and total physical activity measured via an ActivPal accelerometer worn for a 1-week observation period to compare which treatment strategy, HIW or CSW, worked better to reduce frailty (aim #1). Investigators will use the SHARE-Frailty Instrument to evaluate frailty as both a categorical (e.g. non-frail, pre-frail, or frail) and a continuous outcome. This approach will allow investigators to determine how participants move between frailty categories as well as within frailty categories in response to intervention. In aim #2, investigators will determine the effect of walking intensity on mobility, physical functioning, balance, and total physical activity. Investigators hypothesize that HIW participants will show decreased frailty and improved mobility, physical functioning, balance, and physical activity at 4 months. Currently, the optimal physical activity guidelines for older adults with frailty are uncertain. Results from this study will provide important knowledge to inform activity guidelines for older adults with frailty and information on a transformative approach to reducing frailty, improving function, and increasing physical activity among a growing segment of the older adults population.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
200 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
The Effect of High Intensity Walking on Frailty
Actual Study Start Date :
Nov 26, 2018
Anticipated Primary Completion Date :
Aug 31, 2022
Anticipated Study Completion Date :
May 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: High Intensity Walking

HIW (70-80% HRmax)

Behavioral: High Intensity Walking
70-80% HRmax

Experimental: Casual Speed Walking

Self selected pace

Behavioral: Casual Speed Walking
Self selected pace

Outcome Measures

Primary Outcome Measures

  1. Change in frailty as measured by the Survey of Health, Ageing, and Retirement in Europe-Frailty Instrument (SHARE-FI) [Baseline and four months]

    SHARE-FI which assesses fatigue, appetite, weakness, walking difficulties, and low physical activity

Secondary Outcome Measures

  1. Improved mobility as measured by gait speed [Baseline and four months]

    Measures related to overall health and mobility

  2. Improved physical function on the Short Physical Performance Battery [Baseline and four months]

    Provide an overall assessment of functional status and physical performance

  3. Improved balance as measured by the Berg Balance Scale [Baseline and four months]

    The Berg Balance Scale is a valid and reliable 14 item tool to evaluate static and dynamic balance among older adults. Minimum Score 0 to Maximum Score 56. • Score of < 45 indicates individuals may be at greater risk of falling

  4. Total daily physical activity [Baseline and Four Months]

    ActivPal Activity Monitors worn for a one week ambulatory monitoring period, data are sampled at 20 Hz in 10 second intervals.

  5. Improved mobility as measured by Time Up and Go [Baseline and Four Months]

    Measures related to mobility

  6. Improved mobility as measured by 6 Minute Walk Test [Baseline and Four Months]

    Measures related to mobility

  7. Improved balance as measured by the Falls Efficacy [Baseline and Four Months]

    Falls Efficacy Scale as this is a widely-used measure among older adults that evaluates the fear of falling and balance confidence, 10-item questionnaire with scores ranging from minimum score 0 to maximum score 100. A total score of greater than 70 indicates that the person has a fear of falling

Eligibility Criteria

Criteria

Ages Eligible for Study:
60 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • • > 60 years of age with pre-frailty or frailty as determined on the SHARE-FI.

  • Able to ambulate at least 10 feet with moderate assistance (<50% physical assistance) or less. Participants will be able to use their assistive device (e.g. cane or walker) during sessions.

  • Resident of one of the 10 enrolled retirement community locations. Individuals must be > 60 years of age to move into the retirement communities by virtue of the individual community policies.

  • Provision of informed consent and clearance for participation as determined by the Exercise and Screening for You (EASY).

Exclusion Criteria:
  • • Uncontrolled cardiovascular, metabolic, renal, or respiratory disease that limits exercise participation (e.g., previous heart attack within 3 months of enrollment or uncontrolled diabetes)

  • Resting blood pressure > 180/110 mmHg.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Northwestern Univiersity Department of Physical Therapy and Human Movement Sciences Chicago Illinois United States 60611

Sponsors and Collaborators

  • Northwestern University

Investigators

  • Principal Investigator: Margaret Danilovich, PhD, Northwestern University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Margaret Danilovich, Assistant Professor, Northwestern University
ClinicalTrials.gov Identifier:
NCT03654807
Other Study ID Numbers:
  • STU00207757
First Posted:
Aug 31, 2018
Last Update Posted:
Apr 8, 2022
Last Verified:
Apr 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 8, 2022