NCT02580409

Brief Summary

Rehabilitation Enhancing Aging through Connected Health, REACH, is designed to evaluate the benefits of a novel rehabilitative care program on physical function utilizing mobile health technology to deliver patient centered care more efficiently and health care utilization after one year of follow up.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
75

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jan 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

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2015

Completed
10 months until next milestone

First Submitted

Initial submission to the registry

October 14, 2015

Completed
6 days until next milestone

First Posted

Study publicly available on registry

October 20, 2015

Completed
1.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2017

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2017

Completed
8.5 years until next milestone

Results Posted

Study results publicly available

December 15, 2025

Completed
Last Updated

December 15, 2025

Status Verified

December 1, 2025

Enrollment Period

2.3 years

First QC Date

October 14, 2015

Results QC Date

October 4, 2019

Last Update Submit

December 11, 2025

Conditions

Keywords

health care utilizationhealth care costs

Outcome Measures

Primary Outcomes (1)

  • Change in Late Life Function and Disability Index (Function Domain Only)

    The Late-Life Function \& Disability Instrument (Late-Life FDI) is a self-report evaluative outcome instrument for community-dwelling older adults. It is designed to assess and be responsive to meaningful change in two distinct outcomes: function and disability. It is possible to measure one without the other. For this study, only the functional domain will be used. Functional limitations pertain to limitations in a person's ability to do discrete actions or activities. This domain is scaled between 0-100 with higher scores reflecting better mobility. The outcome measure is presented as a coefficient of change within a regression model evaluating baseline and follow up values of the outcome..

    Assessed at baseline visit and 12 months after baseline visit (1 year visit)

Other Outcomes (1)

  • Change in the Short Physical Performance Battery (SPPB)

    Assessed at screen visit, 6 month assessment after baseline visit and 12 months after baseline visit (1 year visit)

Study Arms (1)

Single-arm studies

OTHER

Behavioral Intervention

Behavioral: Exercise Intervention

Interventions

Investigators are proposing an innovative rehabilitative care program for older primary care patients at risk for mobility decline. The program targets newly identified risk factors for mobility decline and utilizes mobile health technology to deliver patient centered care more efficiently. Study participants will receive exercise instruction with a licensed physical therapist for an average of 8-10 training sessions, with the possibility of up to 16 sessions. some at home and some in the clinic. The exercise training sessions will focus on improving mobility, balance and ability to get up from a chair with the use of an exercise application (Wellpepper) being used on a study issued iPad.

Single-arm studies

Eligibility Criteria

Age65 Years - 95 Years
Sexall
Healthy VolunteersYes
Age GroupsOlder Adult (65+)

You may qualify if:

  • Ages 65-95 years
  • Able to understand and communicate in English
  • Difficulty or task modification with walking ½ mile (6 blocks) or climbing one flight of stairs
  • Ability to continuously walk 400 m in less than 15 minutes without stopping for more than a minute at a time, sitting, leaning, or the help of another person
  • Lives in a zip code within 10 mile radius of Spaulding Cambridge Facility
  • Baseline Short Physical Performance Battery (SPPB) scores from 3-12 with \<20% of SPPB scores in the 11-12 range

You may not qualify if:

  • Presence of a terminal disease (e.g. receiving hospice services, metastatic cancer)
  • Major surgery or Myocardial Infarction in the last 6 months
  • Planned major surgery (e.g. joint replacement)
  • Planned move from the Boston area within 1.5 years
  • Mini-mental state exam (MMSE) score \<20
  • Major medical problems interfering with safe and successful testing (examples may include: history hip replacement with recurrent dislocation, uncontrolled hypertension, use of supplemental oxygen)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Spaulding Rehabilitation Hospital Cambridge

Cambridge, Massachusetts, 02138, United States

Location

Related Publications (2)

  • Bean JF, Brown L, DeAngelis TR, Ellis T, Kumar VSS, Latham NK, Lawler D, Ni M, Perloff J. The Rehabilitation Enhancing Aging Through Connected Health Prehabilitation Trial. Arch Phys Med Rehabil. 2019 Nov;100(11):1999-2005. doi: 10.1016/j.apmr.2019.04.015. Epub 2019 May 29.

  • Ni M, Brown LG, Lawler D, Ellis TD, Deangelis T, Latham NK, Perloff J, Atlas SJ, Percac-Lima S, Bean JF. The rehabilitation enhancing aging through connected health (REACH) study: study protocol for a quasi-experimental clinical trial. BMC Geriatr. 2017 Sep 20;17(1):221. doi: 10.1186/s12877-017-0618-x.

MeSH Terms

Conditions

Mobility LimitationPatient Acceptance of Health Care

Condition Hierarchy (Ancestors)

Signs and SymptomsPathological Conditions, Signs and SymptomsTreatment Adherence and ComplianceHealth BehaviorBehavior

Results Point of Contact

Title
Dr. Jonathan Bean
Organization
Spaulding Rehabilitation Hospital

Study Officials

  • Jonathan F Bean, MD, MS, MPH

    Spaulding Rehabilitation Hospital

    PRINCIPAL INVESTIGATOR

Publication Agreements

PI is Sponsor Employee
Yes

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
MD, MS, MPH

Study Record Dates

First Submitted

October 14, 2015

First Posted

October 20, 2015

Study Start

January 1, 2015

Primary Completion

May 1, 2017

Study Completion

July 1, 2017

Last Updated

December 15, 2025

Results First Posted

December 15, 2025

Record last verified: 2025-12

Locations