Actively Recruiting

Phase 2
Age: 18Years - 75Years
All Genders
NCT05317832

Using Smartphones to Improve Physical Activity Levels of Individuals With Spinal Cord Injury

Led by Temple University · Updated on 2025-10-24

196

Participants Needed

1

Research Sites

188 weeks

Total Duration

On this page

Sponsors

T

Temple University

Lead Sponsor

N

Northeastern University

Collaborating Sponsor

AI-Summary

What this Trial Is About

The overarching goal of this research study is to evaluate a sensor-enabled, just-in-time adaptive intervention (JITAI) strategy to increase and sustain physical activity levels among individuals with spinal cord injury (SCI) in their communities. A primary objective of this study is to evaluate the integration of a JITAI with a web-based physical activity intervention program. We hypothesize that the integration of web-based physical activity intervention program with JITAI will result in significantly higher physical activity levels compared to the standard web-based physical activity intervention program alone. A secondary objective of this study is to extend existing algorithms that use commercial wearable technology to robustly detect physical activity behaviors to facilitate the delivery of tailored just-in-time actionable feedback and physical activity recommendations for individuals with SCI.

CONDITIONS

Official Title

Using Smartphones to Improve Physical Activity Levels of Individuals With Spinal Cord Injury

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Be between 18 and 75 years old
  • Have a traumatic or non-traumatic spinal cord injury at cervical level 5 (C5) or below
  • Be at least 6 months post-spinal cord injury
  • Use a manual or power wheelchair as primary mobility for more than 80% of the time
  • Be able to use arms for exercise
  • Show readiness for physical activity based on the Physical Activity Readiness Questionnaire
  • Have experience using a smartphone and a smartwatch
Not Eligible

You will not qualify if you...

  • Have any secondary complications that medically limit activity, such as cardiovascular disease, pressure injuries, contractures, or infections
  • Be diagnosed with traumatic brain injury

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Temple University

Philadelphia, Pennsylvania, United States, 19121

Actively Recruiting

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Research Team

S

Shivayogi V Hiremath, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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