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A Single-Session Intervention for Adolescents and Young Adults with Internalizing Problems

A Single-Session Intervention for Adolescents and Young Adults with Internalizing Problems

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05826392
Enrollment
41
Registered
2023-04-24
Start date
2023-05-01
Completion date
2024-08-13
Last updated
2024-11-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Depressive Symptoms

Keywords

depression, anxiety, growth mindset, neuroplasticity

Brief summary

With the increasing number of adolescents and young adults (AYA) experiencing depression and anxiety, paired with the lack of time, access, and funding towards social services, AYA need a mental health intervention that is affordable and easily accessible. A single-session intervention (SSI), Project Personality, was developed to improve youth growth mindset and reduce symptoms of internalizing problems, such as anxiety and depression. The purpose of this pilot study is to determine the feasibility of an SSI in adolescents and young adults at a reproductive community health center.

Detailed description

The mental health of adolescents and young adults (AYA) has greatly been impacted since the beginning of the pandemic. With the increasing number of AYA experiencing depression and anxiety, paired with the lack of time, access, and funding towards social services, AYA need a mental health intervention that is affordable and easily accessible. A single-session intervention (SSI) focused on cultivating an AYA's growth mindset has potential to overcome common barriers to care, such as cost, transportation and stigma related to psychological treatment. Furthermore, research shows having a fixed mindset correlate and can predict higher depressive and anxiety symptoms. Teaching adolescents about growth mindsets could decrease the risk of internalizing symptoms. The SSI, Project Personality, was developed to improve youth growth mindset and reduce symptoms of internalizing problems, such as anxiety and depression. The purpose of this pilot study is to determine the feasibility of an SSI in adolescents and young adults at a reproductive community health center.

Interventions

OTHERAdolescent/Young Adult Self-Administered Web-Based Single-Session Intervention

Web-Based, 30-minute self-administered intervention for adolescents

Sponsors

Baylor College of Medicine
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Masking description

No blinding

Intervention model description

Adolescents and young adults (AYA), ages 13-24 will receive a 30-minute, web-based single-session program about growth mindset.

Eligibility

Sex/Gender
ALL
Age
13 Years to 24 Years
Healthy volunteers
Yes

Inclusion criteria

* The adolescent or young adult is between the ages of 13 and 24. * The adolescent or young adult has a score above 5 on either PHQ-9 (Patient Health Questionnaire-9) or GAD-7(General Anxiety Disorder-7). * The adolescent and their parent participating in the study, or the young adult can read and comprehend English.

Exclusion criteria

* The adolescent or the young adult has severe current suicidal/homicidal ideation and/or self-injury requiring medical intervention as defined by the ASQ (Ask Suicide-Screening Questions). * The adolescent and their parent participating in the study, or the young adult cannot read or comprehend English. * The adolescent and their parent participating in the study, or the young adult cannot travel to the Baylor College of Medicine (BCM) Teen Health Clinic to receive the single-session intervention.

Design outcomes

Primary

MeasureTime frameDescription
Change in PROMIS (Patient-Reported Outcomes Measurement Information System) Anxiety - AdultBaseline (before treatment); 2 weeks post-treatment; 2 months follow-upAssesses self-reported fear, anxious misery, hyperarousal, and somatic symptoms related to arousal in adults. 8 items are scored with a total score between 8-40.
Change in Short Mood and Feelings Questionnaire-Child (SMFQ-C)Baseline (before treatment); 2 weeks post-treatment; 2 months follow-upThe short version of the self-reported questionnaire that measures depressive symptoms in adolescents 12-17 years old throughout the past 2 weeks. 13 items are scored on a 0-2 scale (0= Not True; 2= True), with a total score between 0-26.
Change in Short Mood and Feelings Questionnaire-Adult (SMFQ-A)Baseline (before treatment); 2 weeks post-treatment; 2 months follow-upThe short version of the self-reported questionnaire that measures depressive symptoms in adults throughout the past 2 weeks. 13 items are scored on a 0-2 scale (0= Not True; 2= True), with a total score between 0-26.
Change in PROMIS (Patient-Reported Outcomes Measurement Information System) Anxiety - ChildBaseline (before treatment); 2 weeks post-treatment; 2 months follow-upAssesses self-reported fear, anxious misery, hyperarousal, and somatic symptoms related to arousal. 7 items are scored with a total score between 8-40.

Secondary

MeasureTime frameDescription
Perceived Primary Control ScaleBaseline (before treatment); 2 weeks post-treatment; 2 months follow-upMeasures perceived control over academic, social, and behavioral outcomes. Scoring for items 1,2,4,7,9,11,14,15,18,20,22, and 24 are as follows: 0= Very False, 1= Sort of False, 2= Sort of True and 3= Very True. Reverse scoring is needed for items 3,5,6,8,10,12,13,16,17,19,21, and 23 and scoring is as follows: 3= Very False, 2= Sort of False, 1= Sort of True, 0=Very True.
Perceived Secondary Control ScaleBaseline (before treatment); 2 weeks post-treatment; 2 months follow-upMeasures the ability to adjust oneself to adverse events and how they control their subjective emotional impact. Scoring for items 1,2,5,7,10,14,17,18, and 20 are the following: 0= Very False, 1= Sort of False, 2= Sort of true and 3= Very True. Reverse scoring is needed for items 3,4,6,8,9,11,12,13,16, and 19 and the responses are as follows: 3= Very False, 2= Sort of False, 1= Sort of True, 0= Very True.
The Acceptance and Action Questionnaire-II (AAQ-II)Baseline (before treatment); 2 weeks post-treatment; 2 months follow-upA scale used to evaluate a participant's (young adult) psychological flexibility. 7 items are scored on a 1-7 scale (1= never true; 5 = always true).
Avoidance and Fusion Questionnaire for Youth-8 (AFQ-8)Baseline (before treatment); 2 weeks post-treatment; 2 months follow-upA scale used to evaluate a participant's (adolescent) psychological flexibility. 8 items are scored on a 0-4 scale (0= not at all true; 4 = very true).

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026