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Completed

NCT Number: NCT00257400

Comparison of Two Psychotherapy Treatments for Depressed Women With a History of Sexual Abuse

This study will compare the effectiveness of individual versus interpersonal psychotherapy in treating depressed women with a history of sexual abuse.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

University of Rochester Medical Center

Rochester, New York, 14642, United States

About this study

Depression is a common but serious mental disorder that affects millions of people each year. Depression can severely impact people's lives, causing them to often feel sad and hopeless, as well as affecting people's sleep patterns, concentration, and energy levels. Women with a history of abuse are at an increased risk for developing symptoms of depression. However, treatments such as interpersonal psychotherapy and individual psychotherapy have been known to reduce symptoms of depression. This study will compare the effectiveness of individual and interpersonal psychotherapy in improving depressive symptoms and daily functioning in depressed women with a history of sexual abuse.

Participants in this study will undergo a two-part screening interview at the Strong Adult Ambulatory Clinic. This screening will include both written questionnaires and face-to-face interviews regarding any experiences of sexual or physical abuse; suicidal thoughts; family relationships; and current attitudes, thoughts, or feelings. Participants who meet all criteria will then be randomly assigned to receive one of two treatments: interpersonal psychotherapy or individual psychotherapy, which is considered usual care. All treatment sessions will be held at the Strong Adult Ambulatory Clinic. Participants assigned to receive interpersonal psychotherapy will attend weekly 50-minute sessions with a therapist. Interpersonal psychotherapy will focus on current interpersonal stressors in daily life, such as difficulties in close relationships or at work. Treatment will also help participants examine the relationship between their mood changes and interpersonal problems. Participants assigned to receive individual psychotherapy will undergo cognitive-behavioral therapy, supportive counseling, or a combination of the two. Participants will work with their therapists to decide upon a treatment plan designed to help changes in mood and other difficulties in daily life. The number and length of treatment sessions for this group will be determined on an individual basis. For all participants, evaluations consisting of questionnaires similar to those from the initial screening will be completed at mid-treatment, post-treatment, and 3 months after treatment.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Meets DSM-IV criteria for unipolar major depressive disorder
  • History of childhood sexual abuse before the age of 18
  • Seeking outpatient psychotherapy treatment in a community mental health center

Exclusion criteria

  • Meets DSM-IV criteria for major depression with psychotic features, bipolar disorder, schizophrenia, or mental retardation
  • Active alcohol or substance abuse within 3 months of study entry date

Treatment and study plan

Interpersonal Psychotherapy (IPT)

Behavioral

Interpersonal Psychotherapy

Individual Psychotherapy

Behavioral

Individual Psychotherapy

Primary outcomes

  1. Hamilton Rating Scale for Depression

    Time frame: Measured at pre-treatment and Weeks 10, 24, and 36

  2. Beck Depression Inventory

    Time frame: Measured at pre-treatment and Weeks 10, 24, and 36

  3. Structured Clinical Interview for DSM-IV Diagnoses

    Time frame: Measured at pre-treatment and Weeks 10, 24, and 36

Secondary outcomes

  1. Social Adjustment Scale

    Time frame: Measured at pre-treatment and Weeks 10, 24, and 36

  2. Medical Outcomes Survey

    Time frame: Measured at pre-treatment and Weeks 10, 24, and 36

  3. Post Traumatic Stress Disorder (PTSD) Symptom Scale

    Time frame: Measured at pre-treatment and Weeks 10, 24, and 36

Sponsors and collaborators

Lead sponsor

University of Rochester

Other

Collaborators

  • National Institute of Mental Health (NIMH)

Registry information

Official study title

Interpersonal Psychotherapy for Depressed Women With Sexual Abuse Histories

Important dates

Study start
2003
Primary completion
2007
Study completion
2007
First posted
Nov 22, 2005
Registry last updated
Jan 3, 2014

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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