Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Using expressive writing to help adults with spinal cord injuries cope with grief

Official title: The Impact of Expressive Emotional Writing on Facilitating Grief Resolution in Adults With Spinal Cord Injury

Run by University of Alabama at Birmingham · NCT06147258 · Data updated 2026-11-12

This study is testing whether a 10-week online writing program can help adults with spinal cord injuries cope with their grief and improve their emotional well-being.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment60 (estimated)
SponsorUniversity of Alabama at Birmingham
Academic / other
Locations1 site (Birmingham, Alabama)
StatusRecruiting
StartedMay 3, 2024
Main results expectedDecember 31, 2026
Study endsDecember 31, 2026
Registry record updatedDecember 24, 2025
Trial IDNCT06147258 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults over 18 years old with a diagnosis of spinal cord injury and limb weakness who can access the internet.

Probably not a fit

Patients with severe cognitive impairments or those currently undergoing psychotherapy may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study evaluates the therapeutic benefits of a 10-week online coach-guided expressive emotional writing program for adults with spinal cord injuries (SCI). Participants will engage in expressive writing to explore and express their feelings related to the grief of losing physical capacity and life goals. The study employs a randomized controlled trial design to assess improvements in psychosocial health, including grief intensity and social participation, using validated assessments. The program is designed for individuals who can access the internet and communicate effectively in English.

Why it matters

Potential benefit: If successful, this program could significantly improve the psychosocial health and grief resolution of adults living with spinal cord injuries.

How similar studies have gone: Other studies have shown promising results with expressive writing interventions, suggesting potential benefits for similar approaches.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria: (1) diagnosis (with evidence) of SCI (traumatic or non-traumatic) with limb weakness; (2) aged \> 18 years; (3) access to the internet and a computer or to a smartphone that can perform videoconferencing, (4) sufficient English language and cognitive proficiency to complete self-report study questionnaires and understand program content in English, and able to communicate verbally or through writing.

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Exclusion Criteria: (1) severe cognitive impairments that prevent online learning and completion of the evaluation; (2) suicidal intent requiring emergency care; (3) consistent psychotherapy within the last 6 months; (4) current or planned participation in psychological therapy or a clinical trial during the study period that could affect the outcomes of the study; or (5) congenital SCI (e.g., spinal bifida)

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Where it's running

  • University of Alabama at Birmingham
    Birmingham, Alabama, United States
    Recruiting

Study contacts

  • Principal investigator: Hon Yuen, PhD — University of Alabama at Birmingham
  • Study coordinator: Hon Yuen, PhD
  • Email: yuen@uab.edu
  • Phone: 205-934-6301

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.