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Completed

NCT Number: NCT00270244

Group Interpersonal Psychotherapy for Depressed Adolescents in School-based Clinics

This study will assess the effectiveness of group interpersonal psychotherapy (IPT-AG) versus treatment as usual (TAU) in improving the treatment of depressed adolescents in school-based health clinics.

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Key information

Age range

12 year–18 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2

About this study

Depression is a serious medical condition. It occurs in people of all ages, but only in the past two decades has depression in children and adolescents been taken seriously. Children and adolescents with depression may exhibit such behaviors as pretending to be sick, refusing to go to school or getting in trouble at school, clinging to a parent or worrying that the parent may die, sulking, or acting in a negative or grouchy manner. A previous study demonstrated that, when administered by clinicians in school-based clinics, individual interpersonal psychotherapy is effective in reducing depressive symptoms and improving global and social functioning. This study will assess the effectiveness of group interpersonal psychotherapy (IPT-AG) versus treatment as usual (TAU) in improving depressive symptoms of adolescents in school-based health clinics.

Participants in this 16-week single-blind study will be randomly assigned to receive either IPT-AG or TAU in a school-based clinic. Participants assigned to receive IPT-AG will attend two to three, 40-minute individual pre-group sessions, followed by 12, 90-minute group therapy sessions and two additional individual sessions-one midway through the group sessions and another upon completion of group therapy. TAU will consist of counseling sessions as regularly conducted by the school clinic social worker and/or referral to another agency. Study visits will occur at baseline and Weeks 4, 8, 12, and 16, or upon early termination. At the end of 16 weeks, participants assigned to receive IPT-AG will continue in a maintenance program in which they will receive IPT-AG once a month for an additional 6 months. All participants will also be assessed 6 and 12 months post-treatment to measure depressive symptoms, global and social functioning, satisfaction with care, and utilization of other services.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Meets diagnostic criteria for major depression, dysthymic disorder, depressive disorder not otherwise specified, or adjustment disorder with depressed mood
  • Score of 24 or greater on the CES-D
  • Score between 10 and 28 on the HRSD
  • Score of 65 or less on the C-GAS
  • English-speaking
  • Parental or legal guardian consent to participate

Exclusion criteria

  • Actively suicidal
  • Score greater than 28 on the HRSD
  • Mentally retarded
  • Any life threatening medical illness
  • Meets diagnostic criteria for current substance abuse, schizophrenia, or bipolar disorder
  • Any evidence of psychosis, conduct disorder, or active eating disorder
  • Currently in active treatment for depression
  • Taking antidepressant medication at the time of baseline assessment
  • Recent death of someone close

Treatment and study plan

Group interpersonal psychotherapy for depressed adolescents (IPT-AG)

Behavioral

Participants assigned to IPT-AG will attend two to three, 40-minute individual pre-group sessions, followed by 12, 90-minute group therapy sessions and two additional individual sessions-one midway through the group sessions and another upon completion of group therapy. Sessions will focus on problems in interpersonal relationships.

Treatment as Usual (TAU)

Behavioral

TAU will consist of counseling sessions as regularly conducted by the school clinic social worker and/or referral to another agency.

Primary outcomes

  1. Depressive symptoms as measured by the Hamilton Rating Scale for Depression (HRSD) and the Center for Epidemiological Studies-Depression Scale (CES-D)

    Time frame: Measured at Month 18

  2. Overall impairment, as measured by the Global Assessment Scale for Children (C-GAS)

    Time frame: Measured at Month 18

  3. Social functioning, as measured by the Social Adjustment Scale-Self-report (SAS-SR)

    Time frame: Measured at Month 18

Secondary outcomes

  1. Short Acculturation Scale for Hispanics, CES-D, HRSD, C-GAS, Clinical Global Improvement, Inventory of Parent and Peer Attachment, Family Adaptation and Cohesions Evaluation Scales III, and the Penn Helping Alliance Questionnaire-Revised

    Time frame: Measured at Month 18

Sponsors and collaborators

Lead sponsor

New York State Psychiatric Institute

Other

Collaborators

  • National Institute of Mental Health (NIMH)

Registry information

Official study title

Group Interpersonal Psychotherapy for Depressed Adolescents (IPT-AG) in School-based Clinics

Important dates

Study start
2005
Primary completion
2008
Study completion
2008
First posted
Dec 26, 2005
Registry last updated
Dec 30, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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