Text Messaging Intervention for Spinal Cord Injury

KA
KA
Overseen ByKerri A Morgan, PhD
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: Washington University School of Medicine

What You Need to Know Before You Apply

What is the purpose of this trial?

The goal of this pilot study is to design and feasibility test a mobile phone text messaging (SMS) self-management intervention for persons with spinal cord injury (PwSCI). The project will focus on providing a 16-week text messaging intervention on the secondary health conditions of bowel/bladder management, pain, pressure injury, and psychosocial health. Our hopes are to reduce the impact of secondary health conditions (SHC) for PwSCI.

The project hopes to test whether the developed self-management program will be feasible and superior to a control group. determine the feasibility and efficacy of the SMS intervention main questions the study aims to answer are:

Participants will:

Complete an initial assessment Participate in a 16-week text messaging program using their mobile phones Complete 4-week check-ins Complete a post assessment

The main question\[s\] it aims to answer \[is/are\]:

\[primary hypothesis or outcome measure 1\]? \[primary hypothesis or outcome measure 2\]? If there is a comparison group: Researchers will compare \[arm information\] to see if \[insert effects\].

Participants will \[describe the main tasks participants will be asked to do, interventions they'll be given and use bullets if it is more than 2 items\].

Who Is on the Research Team?

KA

Kerri A Morgan, PhD

Principal Investigator

Washington University School of Medicine - Program in OT

Are You a Good Fit for This Trial?

This trial is for adults over 18 with a spinal cord injury living in the community. They must be at least 3 months post-injury, have a secondary health condition due to SCI that affects daily life, speak English, and can use a smartphone for texts during the study.

Inclusion Criteria

I live at home, not in a hospital or long-term care facility.
It has been over 3 months since my injury or illness.
I have a secondary health issue like pain or bladder problems affecting my daily life.
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Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Initial Assessment

Participants complete an initial assessment to establish baseline measures

1 week
1 visit (in-person or virtual)

Treatment

Participants receive a 16-week text messaging intervention focusing on secondary health conditions

16 weeks
Weekly check-ins via text

Follow-up

Participants are monitored for safety and effectiveness after the intervention

2 weeks
1 visit (in-person or virtual)

What Are the Treatments Tested in This Trial?

Interventions

  • Motivational text message group
  • Secondary Health Conditions (SHC) text message group

Trial Overview

The study tests a text messaging program designed to help manage secondary health conditions from spinal cord injuries. Over 16 weeks, participants will receive texts about bowel/bladder management, pain, pressure sores, and mental health.

How Is the Trial Designed?

2

Treatment groups

Active Control

Placebo Group

Group I: Secondary Health Conditions (SHC) text message groupActive Control1 Intervention
Group II: Motivational text message groupPlacebo Group1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Washington University School of Medicine

Lead Sponsor

Trials
2,027
Recruited
2,353,000+

The Craig H. Neilsen Foundation

Collaborator

Trials
62
Recruited
3,100+