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Physical DisabilityOTM-PCORINCT01986647

On the Move: Optimizing Participation in Group Exercise

A study testing On the Move exercise - exercise leader, Standard program - exercise leader and On the Move exercise - staff activity personnel in people with Physical Disability, run by University of Pittsburgh at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Community-dwelling older adults fear loss of independence and nursing home placement more than death. Walking difficulty often leads to loss of independence. Exercise is beneficial to physical and mental health and may prevent walking difficulty and promote independence. Read more about this study

Who is it for?
Ages 65 years and olderHealthy volunteers can take part
Conditions the study is for
Physical Disability
What is being tested?
On the Move exercise - exercise leader, Standard program - exercise leader and On the Move exercise - staff activity personnel
Could I receive a placebo?
No, everyone receives an active treatment
How many people
424 participants
Where
1 siteUnited States
Study dates
Dec 2013to Sep 2016
Phase
Interventional
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 65 years and older
  • All sexes
  • Healthy volunteers accepted
  • Older adult

Who may be able to join

  • 65 years of age or older
  • resident of University of Pittsburgh Medical Center Independent Living Facility or senior housing site
  • Ambulate independently for household distance (may use a straight cane)

Who cannot join

  • non English speaking
  • impaired cognition defined as unable to follow 2 step commands
  • plans to leave area in next 4 months
  • progressive neuromuscular disorder
  • any acute illness or medical condition that is not stable
  • inappropriate response on 6 minute walk test

Trial locations and contacts

1 site in 1 country.

United States1 site
  • University of Pittsburgh

    Pittsburgh, Pennsylvania, 15260

Other trials in United States

About this study

Official title: On the Move: Optimizing Participation in Group Exercise to Prevent Walking Difficulty in At-Risk Older Adults

Community-dwelling older adults fear loss of independence and nursing home placement more than death. Walking difficulty often leads to loss of independence. Exercise is beneficial to physical and mental health and may prevent walking difficulty and promote independence. Recognizing the importance of exercise, senior housing facilities offer exercise programs to their residents. The exercise programs are often group-based, seated range of motion exercises that do not challenge the older adult; consequently participation rates and resident satisfaction are low.

If the goal is to improve walking to promote independence than the exercise program should specifically target walking. Therefore, we developed a challenging, group exercise program entitled "On the Move" which focuses on the fundamentals of walking. In this research study we will determine if the On the Move program is better than a standard program at improving walking and promoting independence and if the same benefits can be obtained if the On the Move program is delivered by staff of the senior living facilities instead of an exercise leader. To answer these questions, 400 community-dwelling older adults living in 32 different Independent Living Facilities and Senior High Rises or living in the community and attending senior community centers will be randomly assigned to either the 12 week On the Move group exercise program or the standard group exercise program delivered by either an exercise leader or staff activity personnel. Participants' walking and reported ability to carry out everyday activities (functional ability) will be assessed before and after the 12 week program. We will also assess participant safety and satisfaction with the exercise program and instructor.

The findings from this research study will provide evidence for the value of the On the Move group exercise program and will better inform patient choices regarding participation in exercise programs. If successful in improving walking and promoting independence and acceptable to the older adult, the On the Move program could be incorporated into exercise programming for older adults in community centers, health clubs, and senior residences across the country.

Read the detailed description

This single-blinded cluster randomized trial compares the effectiveness and sustainability of On the Move and a standard group exercise program in 400 community-dwelling older adults. We will also examine the acceptability and risks associated with exercise participation. We will accomplish the objectives by pursuing the following specific aims:

  1. Compare the effects of the On the Move group exercise program to a standard program on self-reported function and disability and walking ability. The On the Move program will produce greater gains in self-reported function and disability (Late Life Function and Disability Index/LLFDI) and walking ability (6-minute walk test/6MWT and gait speed) when delivered by an exercise leader.
  2. When feasible to be delivered by staff activity personnel, explore the effectiveness of On the Move compared to a standard program; and sustainability compared to delivery by exercise leaders (when feasible). Explore barriers to identifying and training staff activity personnel. On the Move delivered by staff activity personnel (when feasible) will produce gains in above outcomes that are greater than the standard program; and comparable to when delivered by an exercise leader.
  3. Compare the acceptability and the risks of the On the Move and standard exercise programs delivered by (a) exercise leaders and (b) staff activity personnel (when feasible). On the Move will result in greater satisfaction and higher attendance rates than the standard program. Attendance rates and satisfaction will be similar for exercise leader and staff activity personnel led programs when feasible to recruit staff personnel. Adverse event (falls, soft tissue injuries, muscle soreness, etc) rates during exercise will be similar between the two groups and the two facilitators when feasible to recruit staff personnel.
  4. Explore potential baseline predictors of benefit and risks of participation in On the Move program to facilitate informed patient decision making. We will be able to identify combinations of baseline physical, psychosocial and demographic factors associated with each of the treatment response and adverse events outcomes.

This single-blinded cluster randomized trial targets community-dwelling older adults residing in Independent Living Facilities and Senior High Rises or living in the community and attending senior community centers. The trial compares type of exercise program (12 week standard group exercise program to the 12 week On the Move group exercise program) and the mode of delivery (exercise leader to staff activity personnel). Primary outcomes include function, disability and walking ability. We will also examine acceptability and risks associated with exercise participation.

Study population We will recruit participants from the Independent Living Facilities (ILFs), Senior Housing sites and from senior community centers.

Interventions:

Exercise program comparison. The On the Move exercise program will be compared to a standard group exercise program. Both exercise programs will be group-based and led by a person. Both programs will be delivered by trained exercise leaders or trained staff activity personnel (only when such a person is available). When a suitable staff activity person is not available, the program will be delivered by one of our exercise leaders. The frequency and duration of the programs are identical (50 minutes, 2 times a week for 12 weeks). The main difference between the standard and the On the Move group exercise programs is the program content which is described below.

The On the Move exercise program is based on principles of motor learning that enhance "skill" or smooth and automatic movement control. The program contains a warm-up (5 minutes), stepping patterns (15 minutes), walking patterns (15 minutes), strengthening exercises (10 minutes), and cool-down exercises (5 minutes). The warm-up and cool down contain gentle range of motion exercises and stretches for the lower extremities and trunk. The stepping and walking patterns are goal-oriented progressively more difficult patterns which promote the timing and coordination of stepping, integrated with the phases of the gait cycle. The strengthening exercises are conducted in sitting and standing and target the lower extremity muscles. The majority of the program will be conducted in standing (40 minutes) with only a small portion conducted in sitting (10 minutes).

The standard group exercise program is based on exercise programs that are currently being conducted at the facilities (i.e. standard of care). The operationally defined program contains a warm-up (5 minutes), upper and lower extremity strength and flexibility exercises (30 minutes), static balance exercises (10 minutes) and a cool-down (5 minutes). The majority of the program will be conducted in sitting (40 minutes) with only a small portion (10 minutes) conducted in standing.

Sustainability of the program: exercise leader and staff activity personnel comparison (Aim 2). The sustainability of the program will be evaluated by assessing the effectiveness of On the Move compared to a standard program when delivered by staff activity personnel and by comparing outcomes obtained by the On the Move program delivered by exercise leaders and staff activity personnel.

Outcomes:

Our main outcomes, function, disability, and walking ability are highly associated with independence and are extremely important to the older adult. Our primary measure of function and disability is the Late Life Function and Disability Instrument (LLFDI) and our main measures of walking ability are Six Minute Walk Test (6MWT) and gait speed. We will also examine confidence in walking (Gait Efficacy Scale), walking under challenging conditions (challenging gait tasks and figure of 8 walk), and gait variability as additional measures of walking ability. All measures will be collected at baseline and immediately following the 12 week intervention by research personnel who are blinded to the intervention group assignment. All testing will be conducted at the ILFs and Senior Housing sites.

Data analysis:

Aim 1:

First, we will perform a multivariate Hotelling t-test to simultaneously compare the baseline to follow-up change in the three primary outcomes between the arms to protect the type I error rate from multiplicity. If significant, subsequent analyses will be performed without further multiplicity adjustment. If not, subsequent comparisons will be performed with a conservative Bonferroni correction at the α=0.05/4=0.0125 level. This protected test approach has been recommended in the statistical literature and used in other exercise intervention trials with multiple outcomes.

Second, we will fit a series of linear mixed models using the SAS® MIXED procedure with baseline to follow-up change in each of the continuous outcomes (LLFDI function/disability, walking ability, other measures of mobility performance) as the dependent variable; intervention arm (standard/On the Move), as the fixed effect of primary interest; baseline value of outcome as an additional fixed effect covariate; and a facility random effect to account for greater similarity of participants from the same facility compared to different facilities and resulting non-independence of observations within facility (ie. clustering). We will construct appropriate means contrasts to estimate difference in gains in the two interventions when delivered by exercise leaders (Aim 1) whose statistical significance of the estimates will serve as formal tests of hypotheses. We will consider adding other baseline measures found to be significantly different between the arms or deemed important as additional fixed effect covariates in the model to assess robustness of the findings. We note that waiting of participants randomized to staff activity personnel classes constitute a group of control participants, if smaller, without any intervention. Therefore, we will perform another sensitivity analysis employing a similar analytic strategy but with three intervention arms (On the Move/Standard/Wait List Control).

Aim 3(a):

We will fit a series of generalized estimating equations (GEE) models(68) using the SAS® GENMOD procedure with each of the dichotomous adverse events, adherence (21+ sessions or ≥90%) and satisfaction outcomes as the dependent variable; a binomial distribution for the outcome and a logit canonical link function; intervention arm, as the effect of primary interest; baseline value of outcome and any other measures found to be different between arms or deemed important as additional fixed effects covariates; and an exchangeable working correlation structure to account for clustering due to facility. We will appropriately construct contrasts to test hypotheses of differential proportions with adverse events based on intervention when delivered by exercise leaders.

Aims 2, 3(b) and 4 Exploratory Analyses

Aim 2:

We propose an analytic strategy with an exploratory philosophy for Aim 2 sustainability aim, because of the uncertainty surrounding our ability to recruit and train a staff activity person to lead a class safely and per protocol.

We will fit a series of linear mixed models using the SAS® MIXED procedure with baseline to follow-up change in each of the continuous outcomes (LLFDI function/disability, walking ability, other measures of mobility performance) as the dependent variable; intervention arm (standard/On the Move), delivery mode (by exercise leader/staff activity personnel) and their interaction as fixed effects of interest; baseline value of outcome and any other measures found to be different between arms or deemed important as additional fixed effects covariates; and a facility random effect to account for greater similarity of participants from the same facility compared to different facilities and resulting non-independence of observations within facility (ie. clustering). We will construct appropriate means contrasts to estimate difference in gains in the two interventions when delivered by staff exercise personnel (Aim 2 effectiveness hypothesis); and difference in gains attributable to On the Move intervention when delivered by exercise leaders and staff activity personnel (Aim 2 sustainability hypothesis). Statistical significance of the estimates will serve as formal tests hypotheses. We note that participants randomized to staff activity personnel had to wait 12 weeks since their baseline assessment and randomization to start the intervention, during which they may have changed; and that they underwent a second baseline assessment immediately prior to starting the exercise intervention. Therefore, we will repeat the above analysis using their second baseline assessment instead of the first one to assess the sensitivity of results.

Aim 3(b):

We will fit a series of generalized estimating equations (GEE) models using the SAS® GENMOD procedure with each of the dichotomous adverse events, adherence (21+ sessions or ≥90%) and satisfaction outcomes as the dependent variable; a binomial distribution for the outcome and a logit canonical link function; intervention arm, delivery model and their interaction as effects of interest; baseline value of outcome and any other measures found to be different between arms or deemed important as additional fixed effects covariates; and an exchangeable working correlation structure to account for clustering due to facility. We will appropriately construct contrasts to test hypotheses of differential proportions with adverse events based on intervention when delivered by staff activity personnel and delivery mode.

Aim 4:

We will perform the exploratory analyses to identify combinations of baseline predictors of treatment response and risks of participating in On the Move program.

Being tested
On the Move exercise - exercise leader, Standard program - exercise leader, On the Move exercise - staff activity personnel, Standard program - staff activity personnel
Keywords
exercise, older adults, mobility disability
Medical subject headings
Motor Activity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • On the Move exercise - exercise leaderBehavioural

    exercise physiologists

  • Standard program - exercise leaderBehavioural

    This is an impairment-based exercise program focusing on flexibility, strength and endurance and is taught by research staff who are PTs, PTAs, or exercise physiologists

  • On the Move exercise - staff activity personnelBehavioural

    this is a group exercise program focusing on the timing and coordination of walking. The program is taught by a person from the facility that the research team trained.

  • Standard program - staff activity personnelBehavioural

    This is an impairment-based exercise program focusing on flexibility, strength and endurance and is taught by a member of the facility that the research staff trained.

Study groups in NCT01986647
Study groupRoleWhat they receive
On the Move Exercise - exercise leaderExperimentalOn the Move group exercise - 2 times per week for 12 weeks. Each session lasts approximately 1 hour. Timing and coordination exercises to improve walking. Led by exercise leader
Receives: Behavioral: On the Move exercise - exercise leader
Standard program - exercise leaderActive comparatorStandard impairment based seated group exercise program. 2 times per week for 12 weeks, approximately 1 hour class. Led by exercise leader
Receives: Behavioral: Standard program - exercise leader
On the Move - staff activity personnelActive comparatorOn the Move group exercise - 2 times per week for 12 weeks. Each session lasts approximately 1 hour. Timing and coordination exercises to improve walking. Led by activity personnel.
Receives: Behavioral: On the Move exercise - staff activity personnel
Standard - staff activity personnelActive comparatorStandard impairment based seated group exercise program. 2 times per week for 12 weeks, approximately 1 hour class. Led by staff activity personnel
Receives: Behavioral: Standard program - staff activity personnel

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in Self-reported Overall Function From Baseline to 12 Weeks

    Late Life Function and Disability Index (LLFDI) overall function. Scores range from 0-100 with higher score representing better function.

    Measured: baseline and 12 weeks

  2. Change in Self-reported Disability From Baseline to 12 Weeks

    Late Life Function and Disability Instrument (LLFDI) disability frequency component. Scores range from 0-100 with higher scores representing better (less) disability.

    Measured: 12 weeks

  3. Change in Gait Speed From Baseline to 12 Weeks

    Gait speed in m/s

    Measured: 12 weeks

  4. Change in Six Minute Walk Distance From Baseline to 12 Weeks

    distance walked in 6 minutes

    Measured: 12 weeks

Secondary outcomes (11)
  1. Number of Participants Who Reported They Benefited a Good Bit or Somewhat From the Class

    Participant satisfaction will be measured by satisfaction surveys and personal interviews. Benefited from class a good bit or somewhat

    Measured: 12 weeks

  2. Number of Participants Who Reported That the Class Was at Least Somewhat Challenging

    Measured by question on the satisfaction questionnaire. Question asked participants to rate how challenging the class was.

    Measured: 12 weeks

  3. Number of Participants Reporting That They Received a Just Right Amount of Individualized Instruction

    Question from satisfaction questionnaire - that asked participants their opinion on the amount of individualized instruction they received.

    Measured: 12 weeks

  4. Number of Participants Who Reported That They Felt Safe or Very Safe During the Exercise.

    Question from the satisfaction questionnaire.

    Measured: 12 weeks

  5. Number of Participants Who Reported They Were Satisfied or Very Satisfied With the Program.

    Question from the satisfaction questionnaire.

    Measured: 12 weeks

  6. Number of Participants Who Reported They Would Definitely or Probably Continue With the Program

    Question from the satisfaction questionnaire.

    Measured: 12 weeks

  7. Change in Figure 8 Walk Test From Baseline to 12 Weeks

    Time it takes to walk a figure 8 around 2 cones 5 feet apart. Greater time in seconds represents poorer performance

    Measured: 12 weeks

  8. Change in Modified Gait Efficacy Scale From Baseline to 12 Weeks

    Confidence in walking was measured by the modified gait efficacy scale (mGES). Scores range from 0-100 with higher scores indicating greater confidence.

    Measured: 12 weeks

  9. Change in Short Physical Performance Battery From Baseline to 12weeks

    Short physical Performance Battery is a performance test that includes gait speed, 5 time sit to stand and standing balance. Scores range from 0-12 with greater scores indicating better performance.

    Measured: 12 week

  10. Change in Stance Time Variability From Baseline to 12weeks

    variability of individual stance times during walking as measured from a electronic walkway. Measured as the standard deviation of all stance times. greater values represent greater variability which is related to poorer outcomes.

    Measured: 12 week

  11. Change in Narrow Walk Time From Baseline to 12 Weeks

    Time to walk narrow pathway. Greater values (times) indicate poorer performance.

    Measured: 12 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 Nov 2013 (estimated)
  2. Study startDec 2013
  3. Primary completionMay 2016
  4. Study completionSep 2016

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
424 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01986647
Sponsor's protocol ID
PRO13090264
Acronym
OTM-PCORI
Status last verified
Dec 2018
First submitted
11 Nov 2013
Last updated
22 Mar 2019
Data monitoring committee
Yes

Publications

  • Brach JS, Perera S, Gilmore S, VanSwearingen JM, Brodine D, Wert D, Nadkarni NK, Ricci E. Stakeholder involvement in the design of a patient-centered comparative effectiveness trial of the "On the Move" group exercise program in community-dwelling older adults. Contemp Clin Trials. 2016 Sep;50:135-42. doi: 10.1016/j.cct.2016.08.003. Epub 2016 Aug 10.

    PubMed 27521806
  • Klatt BN, Perera S, Dunlap PM, Rosso AL, Brach JS. Activity and Participation Are Associated With Future Falls, Hospitalizations, and Emergency Visits in Community-Dwelling Older Adults. Phys Ther. 2024 Oct 2;104(10):pzae087. doi: 10.1093/ptj/pzae087.

    PubMed 38993047
  • Coyle PC, Perera S, Albert SM, Freburger JK, VanSwearingen JM, Brach JS. Potential long-term impact of "On The Move" group-exercise program on falls and healthcare utilization in older adults: an exploratory analysis of a randomized controlled trial. BMC Geriatr. 2020 Mar 16;20(1):105. doi: 10.1186/s12877-020-1506-3.

    PubMed 32178633
  • Brach JS, Perera S, Gilmore S, VanSwearingen JM, Brodine D, Nadkarni NK, Ricci E. Effectiveness of a Timing and Coordination Group Exercise Program to Improve Mobility in Community-Dwelling Older Adults: A Randomized Clinical Trial. JAMA Intern Med. 2017 Oct 1;177(10):1437-1444. doi: 10.1001/jamainternmed.2017.3609.

    PubMed 28806436

Questions about this trial

What is this clinical trial studying?

A study testing On the Move exercise - exercise leader, Standard program - exercise leader and On the Move exercise - staff activity personnel in people with Physical Disability, run by University of Pittsburgh at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 22 Mar 2019. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Yes. Results are posted in the registry (first posted 22 Mar 2019). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in Self-reported Overall Function From Baseline to 12 Weeks (time frame: baseline and 12 weeks). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT01986647, which also lists 4 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Mar 2019; AzTrials last refreshed its copy on 26 Oct 2026.

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