Reducing Depressive Symptoms in Physically Ill Youth

Sponsor

University of Pittsburgh (Other)

Overall Status

Completed

CT.gov ID

NCT00534911

Collaborator

(none)

Enrollment

Locations

Arms

147

Duration (Months)

Patients Per Site

0.3

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Children and adolescents with inflammatory bowel disease (IBD) have high rates of depressive symptoms and more trouble with daily functioning than those without physical illness. The proposed study will investigate if cognitive behavioral therapy (CBT) is better than supportive therapy (SNDT) in reducing emotional distress and improving functioning in youth ages 9-17 with Crohn's disease or Ulcerative Colitis and depression. This study will also assess the effect of CBT on IBD-related factors such as disease severity, medication adherence, and physical-health related quality of life.

Hypothesis

Individuals who receive CBT will show more improvement than individuals who receive SNDT.

Condition or Disease	Intervention/Treatment	Phase
Inflammatory Bowel Disease Depression	Behavioral: Cognitive Behavioral Therapy Behavioral: Supportive Non-directive Therapy (SNDT)	N/A

Detailed Description

Children and adolescents with inflammatory bowel disease (IBD) have high rates of depressive symptoms and more trouble with daily functioning than those without physical illness. Furthermore, the medications used to treat IBR, such as steroids, may induce depression. The proposed study will investigate if cognitive behavioral therapy (CBT) is better than supportive therapy (SNDT) in reducing emotional distress and improving functioning in youth ages 9-17 with Crohn's disease and depression. This study will also be the first to assess the effect of CBT on IBD-related factors such as disease severity, medication adherence, and physical-health related quality of life.

Participants will be carefully evaluated for depression and those who have clinically significant depression will be randomly assigned to either CBT designed for youth with IBD or supportive therapy sessions. Youth in the CBT group will learn new ways of thinking and acting to reduce symptoms of depression focused on the reconstruction of negative or hopeless physical illness narratives. Parents in the CBT group will participate in three family sessions designed to improve family understanding and communication about the physical illness and about risks for developing depression. Children in the supportive therapy condition will receive social support and information about IBD and depression similar to what they would likely receive from social workers in their pediatric medical clinic. Because emotional difficulties such as the experience of depressive symptoms have been linked with the severity and course of IBD symptoms, this information may enable parents to better help their child cope with his/her physical illness. In addition, participants in both groups may experience reduced depression and improved quality of life.

It is predicted that those in the CBT group will benefit by learning effective strategies for coping with IBD and depression, enhancing their social skills, and improving family communication skills while those in the supportive therapy group will benefit by receiving social support and useful information. The proposed study will help determine which psychosocial approach is of greater benefit for depressed youth with IBD and provide a model for integrating behavioral treatment to decrease both emotional and IBD-related suffering into the comprehensive medical care for IBD in the pediatric population.

Aim 1(primary) Are there differences between the two types of therapy in terms of improving depression.

Aim 2 (secondary) Are there differences between the two types of therapy in terms of improving IBD activity, quality of life, and medication adherence? Aim 3) (secondary) Are there differences between the two types of therapy in terms of improving sleep and pain? Aim 4) (exploratory) Are anxiety, steroid use, and gender moderators of treatment outcome.

Study Design

Study Type:

Interventional

Actual Enrollment :

76 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

Reducing Depressive Symptoms in Physically Ill Youth

Study Start Date :

Sep 1, 2007

Actual Primary Completion Date :

Dec 1, 2013

Actual Study Completion Date :

Dec 1, 2019

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Cognitive Behavioral Therapy Primary & Secondary Control Enhancement Training (PASCET)	Behavioral: Cognitive Behavioral Therapy Participants will receive 12 weeks of CBT designed for youth with IBD. During sessions, participants will learn new ways of thinking (e.g., reconstruction of personal physical illness narratives, coping strategies, social skills) and behaving (e.g., positive activities, family communication, sleep hygiene, relaxation) to improve emotional and physical outcomes. Parent sessions will be provided at the beginning, middle, and end of the treatment to improve family understanding and communication about the physical illness and about risks of developing depression. There will also be 6-month booster sessions during follow-up. Other Name: Primary and secondary coping enhancement training (PASCET)
Active Comparator: Supportive Non-Directive Therapy (SNDT) Supportive Non-Directive Therapy	Behavioral: Supportive Non-directive Therapy (SNDT) SNDT is a 12-week non-directive therapeutic intervention. Participants will receive social support and quality information about the warning signs and risk factors for depression. Parent sessions will be provided at the beginning, middle, and end of the treatment to improve family understanding and communication about the physical illness and about risks of developing depression. There will also be 6-month booster sessions during follow-up.

Arm

Intervention/Treatment

Experimental: Cognitive Behavioral Therapy

Primary & Secondary Control Enhancement Training (PASCET)

Behavioral: Cognitive Behavioral Therapy

Participants will receive 12 weeks of CBT designed for youth with IBD. During sessions, participants will learn new ways of thinking (e.g., reconstruction of personal physical illness narratives, coping strategies, social skills) and behaving (e.g., positive activities, family communication, sleep hygiene, relaxation) to improve emotional and physical outcomes. Parent sessions will be provided at the beginning, middle, and end of the treatment to improve family understanding and communication about the physical illness and about risks of developing depression. There will also be 6-month booster sessions during follow-up. Other Name: Primary and secondary coping enhancement training (PASCET)

Active Comparator: Supportive Non-Directive Therapy (SNDT)

Supportive Non-Directive Therapy

Behavioral: Supportive Non-directive Therapy (SNDT)

SNDT is a 12-week non-directive therapeutic intervention. Participants will receive social support and quality information about the warning signs and risk factors for depression. Parent sessions will be provided at the beginning, middle, and end of the treatment to improve family understanding and communication about the physical illness and about risks of developing depression. There will also be 6-month booster sessions during follow-up.

Outcome Measures

Primary Outcome Measures

Change from baseline in CDRS at 3 months [Month 0, Month 3]
Change in Child Depression Rating Scale (CDRS) score from month 0 assessment to three month assessment.

Secondary Outcome Measures

Change from baseline in KSADS diagnosis at 3 months [Month 0, Month 3]
Remission of depressive episode as measured by Kiddie Schedule for Affective Disorders and Schizophrenia (KSADS) from month 0 assessment to 3 month assessment.

Other Outcome Measures

Pediatric Crohns Disease Index [Month 0, Month 3]
Clinician rated instrument of IBD activity which includes symptoms and objective lab results.
Pediatric Ulcerative Colitis Index [Month 0, Month 3]
Clinician rated instrument of gastrointestinal symptoms.
IMPACT 3 [Month 0, Month 3]
Health-related quality life measure. Self report.

Eligibility Criteria

Criteria

Ages Eligible for Study:

9 Years to 17 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Step 1:

ages 9 to 17 inclusive
capable of completing CDI
meeting diagnostic criteria for CD (the date of diagnosis = date of the first diagnostic test confirming CD)
absence of mental retardation by history
having at least one appointment at the GI clinic (this will include patients followed in these clinics as well as those seeking consultation)

Step 2:

CDI or CDI-P greater than or equal to 10 at Step 1.
ages between 9-17 inclusive
having CD

Exclusion Criteria:

history or current episode of bipolar disorder, eating disorder, or psychotic disorder by DSM-IV criteria
mental retardation by history
antidepressant medications within one month of assessment
suicidality with plan or of severity requiring immediate psychiatric hospitalization or significant act involving intentional self-harm (e.g., cutting or overdose, resulting in medical attention)
unacceptable risk for dangerousness to others as indicated by homicidal (or other violent) ideation, intent or plan or action, or use of illegal weapons
current pregnancy by history
substance abuse by history within one month of enrollment other than nicotine dependence
current treatment with CBT or failure of previous CBT trial for depression judged adequate by at least 12 treatment sessions over a period of less than 1 year conducted by an appropriately trained mental health provider using a manual
if currently receiving other psychotherapy modalities willingness to suspend treatment for 12-week acute treatment phase of study