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Recruiting NCT06981598

NCT06981598 Prevention of Psychological Health Problems Via Integrated Operational Support

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Clinical Trial Summary
NCT ID NCT06981598
Status Recruiting
Phase
Sponsor New York University
Condition Depression, Anxiety
Study Type INTERVENTIONAL
Enrollment 5,586 participants
Start Date 2025-03-10
Primary Completion 2028-03-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Cognitive Behavioral Coaching Training

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 5,586 participants in total. It began in 2025-03-10 with a primary completion date of 2028-03-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Sub-clinical behavioral health services in the military are performed by BH technicians, who receive minimal training. Due to this, embedding more technicians in military units is unlikely to benefit service members. Giving technicians training in, and access to, evidence-based interventions (EBI) could make their work more effective. The proposed study is a training trial examining the efficacy of the full integrated operational support (IOS) toolkit (evidence-based interventions for behavioral health), relative to routine care using standard resources, as a prevention resource for active-duty airmen.

Eligibility Criteria

Inclusion Criteria: * Service members seeing a behavioral health (BH) technician. * Currently embedded BH technicians. Exclusion Criteria: * Service members who are not currently seeing a BH technician. * BH technicians who are not embedded or have taken a clinic role.

Contact & Investigator

Central Contact

Kelly Daly, PhD

✉ kd2691@nyu.edu

📞 914-806-5093

Principal Investigator

Amy S Slep, PhD

PRINCIPAL INVESTIGATOR

NYU

Frequently Asked Questions

Who can join the NCT06981598 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Depression, Anxiety. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06981598 currently recruiting?

Yes, NCT06981598 is actively recruiting participants. Contact the research team at kd2691@nyu.edu for enrollment information.

Where is the NCT06981598 trial being conducted?

This trial is being conducted at New York, United States.

Who is sponsoring the NCT06981598 clinical trial?

NCT06981598 is sponsored by New York University. The principal investigator is Amy S Slep, PhD at NYU. The trial plans to enroll 5,586 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology