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OpenTrials
Completed

NCT Number: NCT03257111

Activity Levels and Rehabilitation Outcomes of Patients Post-stroke

Patients admitted to the in-patient rehabilitation center with a diagnosis of stroke will be recruited into the study. The participants will wear two activity monitors (one commercial grade and one research grade) for the duration of their rehab stay. Data from the monitors will be correlated with rehab outcomes, therapy units billed, and length of stay.

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Key information

Age range

20 year–90 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Florida Gulf Coast University, Fort Myers, Florida, United States

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • diagnosis of stroke
  • patient at the Brookdale Center for Healthy Aging & Rehabilitation
  • not greater than maximum assistance to walk 10 feet
  • walking re-training included in the therapy plan of care

Exclusion criteria

  • primary diagnosis other than stroke
  • allergy or reaction to the wrist bands of the activity monitors

Treatment and study plan

activity monitors

Other

activity monitors are worn on the wrist, much like a watch. Data from the activity monitors will be downloaded once a week and at discharge. Normal hospital and therapy activities will not be altered.

Primary outcomes

  1. Physical Activity Level

    Time frame: from the date of recruitment to the date of discharge or up to 45 days whichever comes first

    Amount of physical activity each day and throughout rehab stay as measured by 2 activity monitors beginning at admission and ending at discharge from the facility

Secondary outcomes

  1. therapy units billed

    Time frame: from the date of recruitment to the date of discharge or up to 45 days whichever comes first

    therapy units are billed 15 minute time blocks; the number of each type of unit will be assessed at discharge from the facility

  2. Functional Independence Measure (FIM)

    Time frame: from the date of recruitment to the date of discharge or up to 45 days whichever comes first

    FIM is a standard rehabilitation outcome used in all rehabilitation hospitals; measured at admission and discharge from the facility

Sponsors and collaborators

Lead sponsor

Florida Gulf Coast University

Other

Collaborators

  • Brookdale Center for Healthy Aging & Rehabilitation

Registry information

Official study title

The Correlation Between Activity Levels and Rehabilitation Outcomes of Patients Post-stroke in an In-patient Rehabilitation Center

Important dates

Study start
2017
Primary completion
2020
Study completion
2020
First posted
Aug 22, 2017
Registry last updated
Jul 23, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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