NCT02950090

Brief Summary

MobilWise, a worksite physical activity intervention for employees at high risk for knee osteoarthritis (OA), is being tested in a developmental randomized controlled trial at a collaborating worksite to determine if remotely- coached physical activity counseling can increase and sustain physical activity in this population. Knee osteoarthritis is a major public health problem and a leading cause of disability and work absenteeism/presenteeism in the US workforce. The overarching goal of this program is to develop and disseminate an affordable, efficient, efficacious physical activity intervention to large groups of employees at risk for knee OA. The Mobil Wise intervention is administered by health professionals, who will use data transmitted from an affordable accelerometer-based personal monitor (Fitbit Flex) via customized remote coach interface to 1) allow the remote coach to view and collect physical activity data generated by the personal monitor, and 2) use that data to formulate and provide tailored behavioral support, using motivational interviewing. This project has the potential to have a tremendous impact on improving symptoms and quality of life of persons with chronic knee pain and decreasing the functional limitation, work absenteeism/presenteeism, and soaring healthcare utilization associated with knee OA.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
61

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Sep 2015

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 1, 2015

Completed
1.1 years until next milestone

First Submitted

Initial submission to the registry

October 24, 2016

Completed
7 days until next milestone

First Posted

Study publicly available on registry

October 31, 2016

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 30, 2017

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 30, 2017

Completed
Last Updated

May 24, 2018

Status Verified

May 1, 2018

Enrollment Period

2 years

First QC Date

October 24, 2016

Last Update Submit

May 22, 2018

Conditions

Keywords

Knee symptomsphysical activityFitbitAccelerometerremote coaching

Outcome Measures

Primary Outcomes (3)

  • Accelerometer counts/day;

    Minutes of non-sedentary activity/day

    change from baseline and 3 months

  • Accelerometer counts/day;

    Minutes of non-sedentary activity/day;

    change from baseline to 6 months

  • Accelerometer counts/day;

    Minutes of non-sedentary activity/day

    change from 3 months to 6 months

Secondary Outcomes (1)

  • Fitbit measured physical activity

    6 months of study

Study Arms (3)

MobilWise

EXPERIMENTAL

MobilWise will use data transmitted from an affordable accelerometer-based personal monitor (Fitbit Flex) via Fitabase to: allow a remote coach to view and collect physical activity data generated by the personal monitor, and use that data to formulate and provide tailored behavioral support, using motivational interviewing. The coach has a phone conversation weekly x 12 using motivational interviewing with participants to set goals and encourage activity. Coaches mention patient use of treatment elements (accountability) and will be positively reinforcing for adherent participants, or will include positive statements for those who are not adherent (supportive).Participants are also encouraged to use all the features of Fitbit (social networking, challenges, email reminders).

Behavioral: MobilWise

Fitbit Only

ACTIVE COMPARATOR

will use data transmitted from an affordable accelerometer-based personal monitor (Fitbit Flex) to monitor their own progress and physical activity level without coaching support. Participants are again encouraged to use all the features of Fitbit (social networking, challenges, email reminders) to achieve activity levels.

Behavioral: Fitbit Only

Waitlist Control

NO INTERVENTION

Participants in the waitlist arm have exposure to the usual wellness supports provided by the company: Motiva is the internal corporate wellness program that is under the direction of the Chief Medical Officer. Initiated in 2000, Motiva is staffed by two full- time health professionals and two full-time healthy lifestyle professionals. Motiva provides wellness programming year round on a BCBSIL intranet web page plus an individual page called myMotiva, where self- assessment of health risks, including weight and physical activity behavior, is encouraged. Participating in myMotiva allows individuals to earn up to $200 per year in an incentive program called Wellness Rewards

Interventions

MobilWiseBEHAVIORAL

see arm description for MobilWise above

MobilWise
Fitbit OnlyBEHAVIORAL

see arm description for Fitbit above

Fitbit Only

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • y/o men and women after completion of the Joint ADventure intervention (included only overweight or obese persons over age 18 with chronic knee symptoms)
  • naive to Joint ADventure (no Minimum BMI) but with knee symptoms of pain, aching or stiffness on most days over the past 3 months, and have the ability to ambulate at least household distances (50ft), the ability to speak and read English.

You may not qualify if:

  • no primary diagnosis of fibromyalgia or inflammatory arthritis
  • no co-morbidity that is more functionally limiting than the knee symptoms (e.g. spinal stenosis, peripheral vascular disease or residual effects of stroke)
  • no co-morbid condition (based on medical history review) that contraindicates a physical activity intervention
  • no total joint re- placement surgery within the past 1 year and no plans for total joint replacement in the next 12 months
  • no plans to relocate away from the Chicago-land area in the next 12 months.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Rush University

Chicago, Illinois, 60612, United States

Location

MeSH Terms

Conditions

Osteoarthritis, KneeMotor Activity

Condition Hierarchy (Ancestors)

OsteoarthritisArthritisJoint DiseasesMusculoskeletal DiseasesRheumatic DiseasesBehavior

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 24, 2016

First Posted

October 31, 2016

Study Start

September 1, 2015

Primary Completion

August 30, 2017

Study Completion

August 30, 2017

Last Updated

May 24, 2018

Record last verified: 2018-05

Locations