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RecruitingNCT07579143MC3Updated May 11, 2026

Mental Health Clinician / Chaplain Collaboration

An interventional study of facilitate forgiveness and community connection to address symptoms of moral injury in Moral Injury, sponsored by Central Arkansas Veterans Healthcare System. Recruiting at 2 sites in United States. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2026-05-11.

Sponsored by Central Arkansas Veterans Healthcare System · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Jun 2026, 4 months ago, but the record still lists the study as recruiting.
  • Registered 7 months after the study started (first participant enrolled Apr 2025, registered Dec 2025).
  • Started Apr 2025; still recruiting 1 year 5 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Not applicable
Ages
18 Years to 80 Years
Sex
All
01

Study summary

The goal of this clinical trial is to learn if the intervention can be delivered by VA chaplains and if it is acceptable for veterans who have symptoms of moral injury (guilt, shame, isolation) and are receiving VA mental health treatment. The main questions it aims to answer are:

Can the study team enroll veterans for this intervention and complete data collection? Will veterans complete the intervention?

There is no comparison group.

Participants will will complete a baseline and 6-month interview and participate in up to 12 intervention sessions with a VA chaplain. The intervention will focus on facilitating forgiveness and community connection.

Read the detailed description

Moral injury symptoms include guilt, shame, and self-isolation. Moral injury is also associated with increased suicide risk. Moral injury symptoms are common in Veterans being treated for posttraumatic stress disorder (PTSD) or substance use disorder (SUD) and current treatments do not always improve these symptoms. The Mental Health Clinician / Chaplain Collaboration (MC3) intervention is delivered by VA chaplains who facilitate forgiveness and community reintegration. MC3 is a collaboration between resources in the mental health clinic, chaplain service, and community to support moral injury symptom recovery.

Specific Aims:

  1. Pre-implementation: Adapt the intervention that was originally delivered by community clergy for delivery by VA chaplains. Stakeholders in this process will include VA chaplains and mental health clinicians at the Little Rock and Pittsburgh VAMCs.
  2. Conduct a single arm pilot study (total N = 20 across 2 sites) of the MC3 intervention to assess feasibility, acceptability, and fidelity (primary outcomes).
  3. Post-implementation: Conduct a formative evaluation with stakeholders of the recruitment methods, MC3 intervention, and outcome measures. This information will be used to refine the MC3 intervention and study procedures for a subsequent RCT.

Methodology: The study design is a two site one arm trial. The population is Veterans being treated in specialty mental health or substance use disorder clinics who have symptoms of moral injury. MC3 will be delivered by VA chaplains who will facilitate forgiveness and community reintegration. The primary outcomes are feasibility and acceptability. Quantitative and qualitative data will be collected at baseline and 6-months (end of intervention). Evidence-based quality improvement methods will be used to implement MC3 at the Little Rock and Pittsburgh VA Medical Centers.

02

Conditions studied

  • Moral Injury

Keywords

  • feasibility
  • acceptability
  • single arm trial
03

In context

Stress Disorders, Post-Traumatic

2,239 studies on the registry are indexed under Stress Disorders, Post-Traumatic; 554 are open to participants now.

This study's planned enrollment of 20 is below the median of 70 across 1,858 interventional studies indexed under Stress Disorders, Post-Traumatic.

Browse Stress Disorders, Post-Traumatic studies →

Lead sponsor

Central Arkansas Veterans Healthcare System is the lead sponsor of 14 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • age 18 to 80 years
  • plan to follow-up with a VA mental health clinician for PTSD or SUD treatment within the next three months (therefore allowing for collaboration)
  • positive screen using the 6-item Moral Injury Distress Scale (MIDS) screener. A positive MIDS screen will be defined as being bothered at least moderately by exposure to at least one potentially morally injurious event (witnessing, omission, commission).

Exclusion criteria

Exclusion Criteria:

  • diagnosis of schizophrenia, bipolar disorder, borderline personality disorder, or severe neurocognitive disorder (e.g., dementia, severe TBI). Veterans with borderline personality disorder will be eligible for participation in this study following DBT completion.
  • Planning to start or current participation in a moral injury treatment group or evidence-based psychotherapy (e.g., Prolonged Exposure or Cognitive Processing Therapy).
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
20 participants (estimated)

Study arms

  • Experimental
    Intervention focused on facilitating forgiveness and community connection

    Intervention is delivered by VA chaplains to facilitate forgiveness and community connection in collaboration with mental health clinicians

    Behavioral: facilitate forgiveness and community connection to address symptoms of moral injury

Interventions

  • Behavioralfacilitate forgiveness and community connection to address symptoms of moral injury

    VA chaplain delivered intervention to facilitate forgiveness and community connection in collaboration with mental health clinicians

06

What researchers measure

Primary outcomes

  1. Number referred, enrolled, baseline and 6-month

    referral, enrollment, and baseline and 6-month data collection

    Time frame: 6 months

  2. intervention retention

    number of sessions completed

    Time frame: 6 months

Secondary outcomes

  1. moral injury distress

    Moral Injury Distress Scale: 18 items, minimum score is 0, maximum score is 72, higher score means greater moral distress severity

    Time frame: baseline and 6 months

  2. Religious and spiritual struggles

    Religious and Spiritual Struggles Scale: 5-item Divine subscale, minimum score is 5, maximum score is 25, higher score means greater struggle with relationship with Divine and 4-item Ultimate Meaning subscale, minimum score is 0, maximum score is 20, higher score means greater struggle with meaning/purpose of life

    Time frame: baseline and 6 months

  3. Forgiving others

    Decision to Forgive Scale: 6 items, minimum score is 6, maximum score is 30, higher score means stronger decision to forgive

    Time frame: baseline and 6-months

  4. Self forgiveness

    Self Forgiveness Dual Process Scale: 10 items, minimum score is 10, maximum score is 50, higher score means greater self-forgiveness

    Time frame: baseline and 6-months

  5. PTSD symptom severity

    Post Traumatic Stress Disorder Checklist for DSM-5: 20 items, minimum score is 0, maximum score is 80, higher score means greater post-traumatic stress disorder symptom severity

    Time frame: baseline and 6-months

  6. Depression symptom serverity

    Patient Health Questionnaire - 9: 9 items, minimum score is 0, maximum score is 27, higher score means greater depression symptom severity

    Time frame: baseline and 6-months

  7. Functioning

    Brief Inventory of Psychosocial Functioning: 7 items, one item for each domain and domains include romantic relationships, family relationships, work, friendships and socializing, parenting, education, and self-care. minimum score is 0, maximum score is 6 for each domain, higher score means more trouble in each domain

    Time frame: baseline and 6-months

  8. Post-traumatic growth

    Post-traumatic Growth Inventory: 15 items, 5 domains include appreciation of life, personal strength, new possibilities, relating to others, spiritual and existential change, minimum score is 0, maximum score is 75, higher score means more post-traumatic growth

    Time frame: baseline and 6-months

  9. Social satisfaction

    Social Satisfaction: 3 items, minimum score is 1, maximum score is 5, higher score means more satisfaction

    Time frame: baseline and 6-months

  10. Loneliness

    UCLA Loneliness Scale: 20 items, minimum score is 1, maximum score is 60, higher score means more loneliness

    Time frame: baseline and 6-months

07

Study locations

1 of 2 sites recruiting
  • Central Arkansas Veterans Healthcare System
    Little Rock, Arkansas 72114, United States
    Completed
  • VA Pittsburgh Healthcare System
    Pittsburgh, Pennsylvania 15240, United States
    • Maribeth Wesesky · Contact · maribeth.wesesky@va.gov · 412-295-7017
    • Jin Cheng, MD · Contact · jin.cheng@va.gov
    • Gretchen Hulse, MDiv · Sub investigator
    • Stephanie Gannon, MDiv · Sub investigator
    Recruiting
08

References and documents

Individual participant data

Plan to share: Yes — De-identified data and limited data set data will be shared in consultation with the local research privacy officer and follow strict privacy protocols and approvals, e.g., upon written request and a signed data use agreement from a non-VA investigator. These requests could be to confirm conclusions made in publications, to duplicate statistical analyses or perform additional analysis.

Supporting information: Study protocol, Sap, Icf, Csr, Analytic code

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 11, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07579143
Lead sponsor
Central Arkansas Veterans Healthcare System
Collaborators
VA Pittsburgh Healthcare System
Responsible party
Jeffrey M Pyne (Physician/Research Scientist, Central Arkansas Veterans Healthcare System) — Principal investigator
First posted
May 11, 2026
Start date
Apr 14, 2025
Primary completion
Jun 2026 (estimated)
Completion
Jun 2026 (estimated)
Last update
May 11, 2026

Study contacts

Jeff M Pyne, MD
Contact
jeffrey.pyne@va.gov
501-442-6019

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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