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Self-Administered Web-Based Intervention for Depression and Anxiety

N/A

Waitlist Available

Research Sponsored by Baylor College of Medicine

Eligibility Criteria Checklist

Specific guidelines that determine who can or cannot participate in a clinical trial

Must have

Be younger than 65 years old

Timeline

Screening 3 weeks

Treatment Varies

Follow Up baseline (before treatment); 2 weeks post-treatment; 2 months follow-up

Awards & highlights

Study Summary

This trial is studying an affordable, accessible mental health intervention, Project Personality, to help reduce depression and anxiety in adolescents and young adults. #mentalhealth #mentalhealthintervention

Who is the study for?

This trial is for adolescents and young adults aged 13-24 with mild to moderate depression or anxiety, as indicated by specific scores on mental health questionnaires. Participants must be able to read and understand English. Those with severe suicidal/homicidal thoughts or self-injury, or who can't travel to the clinic are excluded.Check my eligibility

What is being tested?

The study tests a web-based single-session intervention called Project Personality designed to foster a growth mindset and alleviate symptoms of anxiety and depression in young people. It's conducted at a reproductive community health center to assess its practicality.See study design

What are the potential side effects?

Since this is a psychological intervention rather than medication, traditional side effects are not expected. However, discussing sensitive topics may cause temporary discomfort or emotional distress.

Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ baseline (before treatment); 2 weeks post-treatment; 2 months follow-up

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~baseline (before treatment); 2 weeks post-treatment; 2 months follow-up

This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline (before treatment); 2 weeks post-treatment; 2 months follow-up for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.

Primary outcome measures

Change in PROMIS (Patient-Reported Outcomes Measurement Information System) Anxiety - Adult

Change in PROMIS (Patient-Reported Outcomes Measurement Information System) Anxiety - Child

Change in Short Mood and Feelings Questionnaire-Adult (SMFQ-A)

+1 more

Secondary outcome measures

Avoidance and Fusion Questionnaire for Youth-8 (AFQ-8)

Perceived Primary Control Scale

Perceived Secondary Control Scale

+1 more

Trial Design

1Treatment groups

Experimental Treatment

Group I: Adolescent/Young Adult Self-Administered Web-Based Single-Session InterventionExperimental Treatment1 Intervention

Project Personality is a 30- minute, self-administered, web-based single-session intervention that was developed to help adolescents understand what growth mindsets are and provide them with information about self-changing strategies and coping skills (Schleider & Weisz, 2019). Participants learn about how the brain functions (neuroplasticity), how personality is fluid, and read testimonials from other adolescents about how growth mindsets helped them in school and in their personal lives. Participants also have the opportunity to write notes to other youth, providing them with the advantages of using growth mindsets.

Do I qualify?Apply below to find out

Find a Location

Who is running the clinical trial?

Baylor College of MedicineLead Sponsor

1,001 Previous Clinical Trials

6,001,752 Total Patients Enrolled

11 Trials studying Anxiety

2,084 Patients Enrolled for Anxiety

Media Library

Adolescent/Young Adult Self-Administered Web-Based Single-Session Intervention Clinical Trial Eligibility Overview. Trial Name: NCT05826392 — N/A

Anxiety Research Study Groups: Adolescent/Young Adult Self-Administered Web-Based Single-Session Intervention

Anxiety Clinical Trial 2023: Adolescent/Young Adult Self-Administered Web-Based Single-Session Intervention Highlights & Side Effects. Trial Name: NCT05826392 — N/A

Adolescent/Young Adult Self-Administered Web-Based Single-Session Intervention 2023 Treatment Timeline for Medical Study. Trial Name: NCT05826392 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are participants aged 55 and under eligible to partake in this experiment?

"The age parameters for successful enrolment into this medical trial are 13 and 24 years old, respectively."

Answered by AI

Is my eligibility sufficient to enter this trial?

"The ideal participants for this trial are adolescent and young adult individuals with a diagnosis of anxiety, aged 13-24 years. It is estimated that 200 patients will be recruited overall."

Answered by AI

Is there a possibility for new participants to join this clinical experiment?

"According to clinicaltrials.gov, this medical trial is no longer recruiting participants; the initial posting date was May 1st 2023 and the most recent update occured on April 21st of that same year. As an alternative, there are 1402 other studies actively enrolling patients at present."

Answered by AI

What outcome is this investigation attempting to accomplish?

"The primary endpoint of this clinical trial, assessed pre-treatment and post 2 weeks and 2 months, is a shift in PROMIS (Patient Reported Outcomes Measurement Information System) Anxiety - Child. Secondary endpoints include the Perceived Secondary Control Scale, Acceptance and Action Questionnaire-II (AAQ-II), and Avoidance & Fusion Questionnaire for Youth 8 (AFQ-8). These ratings are scored on various scales from 0 to 4 or 1 to 7 depending on the question."

Answered by AI

Recent research and studies

clinicaltrials.govStudy

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

Eric A Storch 2023. "A Single-Session Intervention for Adolescents and Young Adults With Internalizing Problems". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT05826392.

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