Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT06276725 · ClinicalTrials.gov registry record · NA

Writing Wrongs: Expressive Writing for Microaggressions

A NA study of Post Traumatic Stress Disorder and Discriminatory Stress, sponsored by Auburn University.

Completed
Registry status
NA
Development phase
70
Enrollment target
1
Study location

NCT06276725: Completed NA study of Post Traumatic Stress Disorder and Discriminatory Stress, sponsored by Auburn University.

NCT06276725 is a NA study of Post Traumatic Stress Disorder and Discriminatory Stress that has completed, run by Auburn University. The registered enrollment target is 70 participants, below the 664-participant average among 262 other Post Traumatic Stress Disorder trials with a reported enrollment target (89% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06276725, a NA study of Post Traumatic Stress Disorder and Discriminatory Stress, has completed, sponsored by Auburn University.

COMPLETED
Registry status
NA
Development phase
70 participants
Enrollment target
1
Study location

Study Summary

Racial and ethnic based stressors, such as microaggressions, are pervasive, distressing, and result in lasting negative repercussions for minoritized students at predominantly white institutions (PWIs). These racial and ethnic based stressors are experienced in addition to the universally experienced stressors of higher education. Negative repercussions of microaggressions include increased drop out or transfer rates, distress, fatigue resulting in decreased academic performance, and depression and posttraumatic stress symptoms. Expressive writing (EW) may be a scalable intervention for addressing the negative repercussions resulting from microaggressions experienced by minoritized students at PWIs. Previous research suggests that EW for stressful life events results in benefits such as reduced depression and posttraumatic stress symptoms, improved coping strategies, and reduced activity restriction. Despite such benefits, EW was not designed to specifically address microaggressions in a minoritized student population. Informed by the ADAPT-ITT model, our research group conducted a pilot study with similar procedures. This pilot study demonstrated the acceptability of an adapted version of the EW intervention titled Writing Wrongs (WW), as well as recommended future modifications for WW. In the current study we aim to conduct a randomized-controlled trial to establish the efficacy of WW in alleviating clinical symptoms. We hypothesize that WW will improve symptoms of racial and discriminatory trauma and symptoms of depression, anxiety, and posttraumatic stress over time and compared to an assessment-only condition. We will conduct exploratory analyses to examine short-term changes in affect within and across sessions and across conditions. We will recruit minoritized students enrolled at a PWI. Participants will complete a pre-intervention assessment prior to being randomized into the two conditions. Participants in the intervention condition will engage in three se

Primary Outcome

Trauma Symptoms of Discrimination Scale; range: 0-63; higher score is greater distress associated with discrimantory experiences

Interventions

  • BEHAVIORAL Writing Wrongs

Study Locations (1)

Alabama

  • Auburn University - Auburn

Trial Details

FieldValue
Enrollment Target 70 participants
Start Date 2024-03-18
Est. Completion 2024-12-31
Phase NA
Auburn University

54 total trials

What the finished NCT06276725 record still lists

NCT06276725 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 70 participants, a relatively small participant target, below the 664-participant average among 262 other Post Traumatic Stress Disorder trials with a reported enrollment target (89% lower).

The record links to 3 conditions, with Post Traumatic Stress Disorder appearing as the primary indexed condition, and to 1 intervention - of which Writing Wrongs is the first listed.

NCT06276725 reports a single indexed study location in Alabama.

Frequently Asked Questions

What is clinical trial NCT06276725 about?

NCT06276725 is a clinical study titled "Writing Wrongs: Expressive Writing for Microaggressions". Racial and ethnic based stressors, such as microaggressions, are pervasive, distressing, and result in lasting negative repercussions for minoritized students at predominantly white institutions (PWIs). These racial and ethnic based stressors are experienced in addition to the universally experience...

What is the current status of trial NCT06276725?

This trial is currently completed. It is a NA study. The enrollment target is 70 participants. The study started on 2024-03-18. Estimated completion is 2024-12-31.

What conditions does trial NCT06276725 study?

This clinical trial studies the following conditions: Post Traumatic Stress Disorder, Discriminatory Stress, Microaggression.

What interventions are being tested in trial NCT06276725?

The interventions under investigation include: Writing Wrongs (BEHAVIORAL).

Who is sponsoring clinical trial NCT06276725?

This trial is sponsored by Auburn University, which has 54 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06276725 being conducted?

This trial has 1 study location across Alabama. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Post Traumatic Stress Disorder

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06276725's enrollment target sits among peer trials

70 152nd of 262 higher than 110 of 262 other Post Traumatic Stress Disorder trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Post Traumatic Stress Disorder trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00969111 · 70 participants · NA

    Postoperative or Salvage Radiotherapy (RT) for Node Negative Prostate Cancer Following Radical Prostatectomy

  • NCT01712620 · 70 participants · Phase 2

    Spironolactone for Pulmonary Arterial Hypertension

  • NCT02143830 · 70 participants · Phase 2

    HSCT for Patients With Fanconi Anemia Using Risk-Adjusted Chemotherapy

  • NCT02601339 · 70 participants

    NIRS Monitoring in Premature Infants

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT06276725, the US trial registry maintained by the National Library of Medicine. NCT06276725 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.