A Pilot Trial of Interpersonal Psychotherapy for the Treatment of Depression in Patients With Prostate, Colorectal, Lung and Pancreatic Cancer

Phase

N/A

Condition

Prostate Cancer

Lung Cancer

Colorectal Cancer

Treatment

N/A

Clinical Study ID

NCT01940237

6397

Ages 18-75
All Genders

Study Summary

There is now overwhelming evidence documenting the efficacy of psychotherapy in the treatment of depression in the general population. Surprisingly, however, given the high prevalence of depression in cancer patients, there are very few studies on the efficacy of psychotherapy in this population. Published studies of psychotherapy in cancer patients generally include patients with high heterogeneity of psychiatric diagnosis and frequently include patients without a psychiatric diagnosis, with the aim of preventing the appearance of a psychiatric disorder. This heterogeneity complicates the interpretation of the efficacy and specificity of these interventions. Specifically, the efficacy of psychotherapy for major depression in patients with cancer is unknown.

Eligibility Criteria

Inclusion

Inclusion Criteria:

A primary psychiatric diagnosis of Major Depressive Disorder as defined by DSM-IV
Diagnosis of prostate, colorectal, lung or pancreatic cancer (stage 1-4)
A score of 16 or above in the 17-item HAM-D (Hamilton depression scale)
Male or female ages 18-75.
Ability to give consent
English and/ or Spanish Speaking

Exclusion

Exclusion Criteria:

Lifetime history of psychosis or bipolar disorder
History of substance abuse or dependence in the three months prior to the study.
Current suicide risk.
Patients who have ever failed IPT in the context of cancer.
Patients who are receiving effective medication for depression
Patients with T3, T4 and THS abnormal values

Study Design

April 01, 2012

May 31, 2015

Study Description

Interpersonal psychotherapy (IPT) is a brief, manualized therapy that has shown efficacy in the treatment of major depressive disorder (MDD) in several controlled trials. This study will test the efficacy of IPT in a group of prostate, colorectal, lung and pancreatic cancer patients with a diagnosis of major depressive disorder.

We will test the efficacy of IPT using a variety of outcome measures at different time points of the treatment. Those scales will evaluate the patient's depressive symptoms, psychosocial functioning and quality of life. Patients that are deemed eligible for the study will have IPT for twelve weeks. Patients will receive twelve 50-minute sessions over 16 weeks. To facilitate access to treatment, sessions 1,2,3,4, 8 and 12 will be in person, while all others will in be person or over the telephone according to the patient's choice. Sessions will be audiotaped and periodically reviewed by experienced supervisors to assess therapist's adherence to IPT technique. This taping will be optional and is covered in a separate consent form. This pilot study is to prove feasibility and acceptability of IPT in this population and to show preliminary efficacy.

Connect with a study center

New York State Psychiatric Institute
New York, New York 10032
United States
Site Not Available

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