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Integrated Behavioral Health Innovations in Childhood Chronic Illness Care Delivery Systems

NYU Langone Health logo

NYU Langone Health

Status

Withdrawn

Conditions

Inflammatory Bowel Disease

Treatments

Behavioral: Treatment as usual
Behavioral: Integrated Brief Behavior Therapy (IBBT) Intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT02740309
15-01065

Details and patient eligibility

About

Study design: At baseline, all adolescents and young adults with IBD ages 12-21 years will be screened for anxiety and depression symptoms using the PHQ-9 and the Screen for Child Anxiety Related Disorders (SCARED) during a routine medical visit in the pediatric gastroenterology clinic. Individuals who screen positive for depression or anxiety will be assessed to confirm diagnoses using the anxiety and M.I.N.I. 6.0. Participants will also complete a psychosocial risk assessment as well as medical and socio-demographic inventories. The investigators will include youth that meet full criteria for major depressive disorder and any anxiety disorder, dysthymic disorder, and any adjustment disorder. The investigators will also include patients with subclinical symptoms that have significant psychosocial stressors in addition to their medical illness. Patients will be excluded if they have active suicidal ideation with plan requiring ER referral, bipolar disorder, psychosis, substance dependence, eating disorders, or significant intellectual disability/developmental delay. Participants meeting inclusion criteria will be randomly assigned to four sessions of IBBT administered on-site by a Fink social worker or treatment as usual (TAU), which is a facilitated community referral for mental health treatment.

Sex

All

Ages

12 to 21 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All adolescents and young adults with IBD ages 12-21 years will be screened for anxiety and depression symptoms and includes youth that meet full criteria for major depressive disorder and any anxiety disorder, dysthymic disorder, and any adjustment disorder. The investigators will also include patients with subclinical symptoms that have significant psychosocial stressors in addition to their medical illness.

Exclusion criteria

  • Patients will be excluded if they have active suicidal ideation with plan requiring ER referral, bipolar disorder, psychosis, substance dependence, eating disorders, or significant intellectual disability/developmental delay.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

0 participants in 2 patient groups

Integrated Brief Behavior Therapy (IBBT) Intervention
Experimental group
Description:
4-sessions of IBBT for youth anxiety and depression.
Treatment:
Behavioral: Integrated Brief Behavior Therapy (IBBT) Intervention
Treatment as usual
Active Comparator group
Description:
Treatment as usual
Treatment:
Behavioral: Treatment as usual

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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