Smartphone Technology and E-Coaching for Spinal Cord Injury
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial aims to help people with spinal cord injuries (SCI) become more active through a smartphone app and e-coaching. Participants will follow an exercise program using either a non-interactive exercise app or a customized interactive app. Those who struggle to meet exercise goals will receive additional coaching, based on motivational interviewing, to enhance motivation and adherence. The trial suits individuals with SCI who use a wheelchair or have difficulty walking and wish to increase their exercise levels but are not currently following exercise guidelines. Participants must have a smartphone and be willing to use the study apps.
As an unphased trial, this study provides a unique opportunity for participants to contribute to innovative research aimed at improving exercise engagement for those with SCI.
Do I need to stop my current medications for this trial?
The trial information does not specify whether you need to stop taking your current medications. It seems focused on exercise and app usage, so it's best to consult with the trial coordinators for specific guidance.
What prior data suggests that this smartphone technology and e-coaching method is safe for individuals with spinal cord injury?
Research shows that using mobile health (mHealth) apps to manage spinal cord injuries is generally safe and well-received. Studies on apps similar to the one being tested have found that they help people manage their health without major safety issues. For example, a review of mHealth apps for spinal cord injuries found them easy to use and helpful.
Simpler apps with basic features have also been studied without major problems. They allow users to track their activities and progress easily.
Regarding the e-coaching component, both the twice-a-month and four-times-a-month e-coaching plans aim to motivate and improve exercise habits. Although specific safety data on e-coaching is limited, its personalized support is designed to keep users engaged with minimal risk.
Overall, these technologies are designed to be easy to use and safe, aiming to boost physical activity without adding new health risks.12345Why are researchers excited about this trial?
Researchers are excited about this trial because it explores how smartphone technology can enhance exercise adherence for people with spinal cord injuries. Unlike traditional rehabilitation programs that often rely on in-person sessions, this trial uses apps to offer a more accessible and personalized approach. The interactive app allows users to engage more deeply with their exercise routines, while motivational e-coaching in Stage-II offers tailored support for those who struggle to keep up. These features aim to empower individuals by providing flexibility and continuous support, potentially leading to better long-term outcomes.
What evidence suggests that this trial's treatments could be effective for increasing physical activity in individuals with spinal cord injury?
Research has shown that a smartphone app can help people with spinal cord injuries (SCI) maintain their exercise routines. In this trial, participants will use either an interactive or non-interactive app for self-monitoring. These apps aim to keep users active by focusing on specific habits. Early results from other studies suggest that adding e-coaching, which provides personalized motivational support, can further boost exercise participation. In this trial, non-adherent participants will receive e-coaching two or four times a month. Studies have found that such support improves adherence to exercise plans. This combination of technology and support helps people with SCI become more active.13467
Are You a Good Fit for This Trial?
This trial is for individuals aged 18-80 with a spinal cord injury (SCI), their caregivers, or clinicians who treat SCI patients. Participants must speak English and be willing to download and use study apps on their smartphones.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Technology Development
Focus groups with participants, caregivers, and clinicians to customize smartphone-based apps for exercise adherence.
Usability Testing
Conduct a usability study of custom apps to optimize their acceptability, appropriateness, and feasibility.
Stage-I SMART Trial
Participants use either a non-interactive or interactive app for exercise adherence, with regular updates for Group 2.
Stage-II SMART Trial
Non-adherent participants receive e-coaching to improve exercise adherence.
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- E-Coaching 2x per month
- E-Coaching 4x per month
- Self monitoring using Interactive App
- Self monitoring using Non-interactive App
Trial Overview
The study tests how well a customized interactive smartphone app and e-coaching can help people with SCI stick to exercise guidelines. It starts by comparing two types of apps, then adds motivational e-coaching for those not meeting goals.
How Is the Trial Designed?
2
Treatment groups
Experimental Treatment
After 12 weeks, the participants will be categorized as adherents or non-adherents based on their rates of adhering to the SCI exercise guidelines during Stage-I. Non-adherents (those who met the exercise guidelines \<50% of the weeks) will be randomized to receive an augmented intervention of motivational interviewing-based e-coaching (2x per month or 4x per month) in addition to their Stage-I assigned app for 12 weeks (weeks 13-24) to further increase rates of exercise. All non-adherents who will be assigned to the e-coaching interventions will be asked to complete at least daily EMA surveys. A coach who is trained in motivational interviewing will review the EMA data and work collaboratively with participants to identify barriers and facilitators and develop individualized strategies to improve exercise adherence. Adherents (those who met the exercise guidelines \>50% of the weeks) will continue with only their Stage-I assigned app intervention throughout Stage-II.
Participants will be randomized into one of two groups: Group 1 (self monitoring using a non-interactive app), and Group 2 (self monitoring using an interactive app). Participants in both groups will be provided a customized exercise program to complete over the duration of the study. Within either app, participants will be able to view assigned exercises, log additional exercises completed, complete questionnaires as needed, and access additional resources. Participants will use their own smartphone to receive the health app. Participants will continue using their Stage-I app intervention for the entire duration of the study (weeks 1-24).
Find a Clinic Near You
Who Is Running the Clinical Trial?
Shirley Ryan AbilityLab
Lead Sponsor
Published Research Related to This Trial
Citations
Improving Adherence to Spinal Cord Injury Exercise Guidel...
Aim 3.2: Compare effects of two augmented interventions on primary and secondary outcomes: Groups 1a and 2a (e-coaching twice per month) vs.
2.
withpower.com
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