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Study of Web- Based Cognitive Behavioral Therapy for Depressed Korean Adolescents

Study of Web-based Cognitive Behavioral Therapy in Adolescent Depression; Randomized Controlled Trial for Korean Adolescents

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02072304
Acronym
wogyeokdajim
Enrollment
164
Registered
2014-02-26
Start date
2014-01-31
Completion date
2015-05-31
Last updated
2014-02-26

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

Conditions

Cognitive Behavioral Therapy, Depression, Mental Disorder in Adolescence

Keywords

mood disorder, depressive disorder, mental disorders, program acceptability, behavioral symptoms, suicidal ideation, patient adherence

Brief summary

The purpose of this study is to develope web-based cognitive behavioral therapy for Korean adoldescents who have a mild depression. And we will investigate whether web-based cognitive behavioral therapy is more effective than supportive psychotherapy for treating depressed adolescents. Our hypothesis is web- based cognitive behavioral is more effective than supportive psychotherapy

Detailed description

We will recruit adolescents(age 12-18 years old) with a diagnosis of major depressive disorder, dysthymia and depressive disorder NOS in outpatient clinic of child and adolescent psychiatry and we will advertise for recruitment of subjects in community. The study protocol will be approved by the Institutional Review Board of the Hallym university sacred heart hospital. Well- trained interviewers will conduct the assessments of participants and their parents or guardians. The assessment included the diagnostic interview, demographic characteristics, depressive symptom severity scale , Columbia suicide severity rating scale, questionnaire about abuse histories. We decided the number of participants of 164, because in previous studies, web- based cognitive behavioral therapy showed mild to moderate effect size (effect size = 0.43). So for examining the hypothesis, we will recruit 164 adolescents by calculating the number of participants using G power program version 3.1.3. (level of significance = 5%, power of a hypothesis test = 80%, drop out rate = 20%) And we will conduct randomized controlled trial for examining the efficacy of web- based cognitive behavioral therapy. Our hypothesis is web- based cognitive behavioral is more effective than supportive psychotherapy, so we will deliver web- based cognitive behavioral therapy program to cognitive behavioral therapy group for 8 weeks(once in a week), and supportive psychotherapy to supportive psychotherapy group for 8 weeks(once in a week) We will exclude the participant if the participant has severe depressive symptoms, definite suicidal idea, plan and attempt, psychotic symptoms, bipolar disorders, sexual abuse histories, other neurological diseases or received cognitive behavioral therapy, pharmacotherapy or interpersonal psychotherapy. We will analyze the intent- to- treat population. For each individual, missing values are replaced by the last observed value of that variable. And we will use Chi square test or repeated measure-ANOVA.

Interventions

BEHAVIORALweb-based CBT

A cognitive behavioral program in 8 weeks that will provide participants with the following: online interactive tools to do their homeworks and guidance on using cognitive and behavioral strategies to help reduce depressive symptoms, information about the depressive symptoms and cognitive behavioral therapy

BEHAVIORALsupportive care

supportive care group will receive supportive care for treating depression by e-mail per a week for 8 weeks with the following: psychoeducation about depression, stigma of mental illness, distraction technique, emotional regulation, active scheduling.

Sponsors

Hallym University Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
12 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Clinical diagnosis of major depressive disorder, dysthymic disorder and depressive disorder NOS * participants and their parents both agree informed consents

Exclusion criteria

* participants have psychotic symptoms, developmental disorders, * participants are diagnosed by bipolar disorder * participants are current high risk of suicide * participants have psychiatric and physical symptoms need urgent medicine treatment * participants have a history of sexual abuse * participants have cognitive behavioral therapy or interpersonal psychotherapy within 3 months * participants have a history of brain injury or a neurological disorder such as seizure disorder, or severe physical disorder

Design outcomes

Primary

MeasureTime frameDescription
The Center for Epidemiological Studies of Depression (CES-D) Scale0, 4, 8 weeksChange in CESD from baseline Change in CESD scale between and within groups across the 8 weeks and for each assessment point
Subjective depressed mood scaleeach week during 8 weeksChange in Subjective depressed mood scale from baseline Change in Subjective depressed mood scale scale within web CBT groups across the 8 week
The Korean youth self report (K-YSR)0, 8 weeksChange in K-YSR from baseline Change in K-YSR scale between and within groups across the 8 weeks

Secondary

MeasureTime frameDescription
Acceptability and adherence of Web-based cognitive behavioral treatment program for adolescents with depression8 weeksAfter treatment, we will check out how many the participants complete the session.
Adolescent's characteristics that moderate the impact of the program0, 4 and 8 weeks after baseline assessmentwe will find out adolescent's characteristics that moderate the impact of the program
satisfaction of Web-based cognitive behavioral treatment program of both adolescents with depression and their parents8 weekAfter treatment, we will check out how the participants and their parent feel satisfaction about treatment
Columbia suicide severity rating scale0, 4 8 weeks after baseline assessmentChange in CSSRS from baseline Change in CSSRS scale between and within groups across the 8 weeks and for each assessment point

Countries

South Korea

Contacts

Primary Contacthyori jang, RN
hypray85@naver.com10-31-381-3753
Backup Contactsong-ii ahn, MD
ahnsongii83@gmail.com10-31-380-3750

Outcome results

None listed

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