Resiliency Training on the College Campus

NCT ID: NCT06038786

Last Updated: 2023-09-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

107 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-07-01

Study Completion Date

2020-03-01

Brief Summary

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This is a waitlist controlled study examining the initial efficacy of Resilience Training among college students at an elevated risk for a severe mental illness.

Detailed Description

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Conditions

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Psychotic Disorders Mood Disorders Anxiety Disorders

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Waitlist controlled design
Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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Resilience Training

Participants obtained Resilience Training, a 4 session, 1.5 hour group intervention delivering the following skills: mindfulness, mentalization, and self-compassion.

Group Type EXPERIMENTAL

Resilience Training

Intervention Type BEHAVIORAL

A 4 session group-based behavioral intervention which delivers the following skills: mindfulness, metallization, and self-compassion.

Waitlist

A 4-6 week waitlist during which participants did not receive any treatment. They would then obtain Resilience Training following their waitlist period.

Group Type PLACEBO_COMPARATOR

Resilience Training

Intervention Type BEHAVIORAL

A 4 session group-based behavioral intervention which delivers the following skills: mindfulness, metallization, and self-compassion.

Interventions

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Resilience Training

A 4 session group-based behavioral intervention which delivers the following skills: mindfulness, metallization, and self-compassion.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

1. 18-30 years old
2. Enrolled in undergraduate program at the college or university where the intervention takes place
3. Students who endorse delusion-like experiences (DLEs): Peter's et al. Delusion Inventory (PDI) score \> 4 and/or
4. Students with mild to moderate depressive symptoms: Beck Depression Inventory (BDI) score ≥ 6

Exclusion Criteria

1. Inability to provide informed consent
2. Not proficient in English
3. Current self-reported Diagnostic Statistical Manual 5 (DSM-5) diagnosis with active symptoms (such as active psychotic symptoms, current suicidality, serious active alcohol or substance use, marked deterioration in functioning over the prior month) determined by clinical interview with participant, or self-report of a psychiatric diagnosis that necessitates close monitoring or individual therapy and/or inpatient or partial hospitalization
4. Current enrollment in psychological or behavioral health treatment.
5. Current use of psychotropic medications (other than stimulants) prescribed by a physician.
Minimum Eligible Age

18 Years

Maximum Eligible Age

30 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Massachusetts General Hospital

OTHER

Sponsor Role lead

Responsible Party

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Daphne Holt

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Daphne Holt, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Massachusetts General Hospital

Locations

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Massachusetts General Hospital

Charlestown, Massachusetts, United States

Site Status

Countries

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United States

References

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DeTore NR, Burke A, Nyer M, Holt DJ. A Brief Resilience-Enhancing Intervention and Loneliness in At-Risk Young Adults: A Secondary Analysis of a Randomized Clinical Trial. JAMA Netw Open. 2024 Feb 5;7(2):e2354728. doi: 10.1001/jamanetworkopen.2023.54728.

Reference Type DERIVED
PMID: 38315488 (View on PubMed)

Other Identifiers

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2016P002351

Identifier Type: -

Identifier Source: org_study_id

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