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NCT04952532Completed

A Novel Cognitive Remediation Intervention Targeting Poor Decision-making and Depression in Veterans at High Risk for Suicide: A Safe, Telehealth Approach During the COVID-19 Pandemic

Source: ClinicalTrials.gov · Last updated 26 Jan 2026

Brief summary (registry, in English)

Despite large-scale, nationwide efforts to better address suicidal behavior in Veterans at high risk, the development of interventions that target some of the key risk factors associated with suicide remains limited. This study aims to collect pilot data to test feasibility/acceptability of a novel adjunctive evidence-based cognitive remediation (CR) therapy with manualized "Bridging" sessions for transfer and practice of problem-solving strategies for real-world stressors, including those that trigger suicidal thoughts. This 10-week (20 session) Neuropsychological Educational Approach to Cognitive Remediation CR+Bridging telehealth intervention will be administered virtually via HIPPA-compliant services to 36 Veterans with major depressive disorder and a history of suicide attempt(s). Pre-, post-treatment, and follow-up assessments of neurocognitive, clinical, social, and real-world functioning also will be conducted. This study has potential for high public health impact and promise to help improve quality of life for Veterans at high risk for suicide.

Status (registry)
Completed
Study type
Interventional
Enrollment
9 (actual)
First submitted
2 Jul 2021
Start date
1 Jan 2022
Primary completion date
31 Dec 2024
Lead sponsor
VA Office of Research and Development
Diseases
Depression
NCT number
NCT04952532

What you commit to

  • Study type: Interventional
  • Participants enrolled: 9
  • From 1 Jan 2022 to the primary completion date, 31 Dec 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Current substance use disorder;
  • History of traumatic brain injury; neurological disorder, or other medical confound; compromised intellectual abilities (WASI45 FSIQ\<70)

Other

  • The investigators will enroll six Veterans in each group and conduct six 10-week intervention cycles for a total sample of 36 Veterans.

Who the study is looking for

  • U.S. Veteran;
  • Primary diagnosis of major depressive disorder (MDD) and a history of suicide attempt in the past year;
  • Elevated score (\>1SD above the normal mean) on rumination measure (Ruminative Response Scale);
  • Based on the Columbia-Suicide Severity Rating Scale (C-SSRS) current suicidal ideation (either passive, i.e. "wish to be dead") or active ideation but with no intent to act on it immediately and no specific plan;
  • Currently in psychotherapy treatment as usual (TAU) at the James J. Peters VA Medical Center.
  • The investigators will include women and aim for the sample to be 30% women.

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
James J. Peters VA Medical Center, Bronx, NY
Coordinator of this site? Confirm its status
The BronxUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.