HOME  | CONTACT  | PATIENT LOGIN  | CLINIC LOGIN  | FAQ
  • PATIENTS &
    HEALTHY VOLUNTEERS
  • INVESTIGATORS
  • CROS / SPONSORS
  • CAREERS
  • TRIAL ALERTS

TRIALS SEARCH
      
  • HEALTH NEWS

  • RSS FEEDS

  • ABOUT TRIALS

  • LINK TO US


View Clinical Trial (Medical Research Study)


Intensive Treatment of Adolescent Panic and Agoraphobia

Signup
Browse Studies

City:   Boston
State:   Massachusetts
Zip Code:   02215
Conditions:   Panic Disorder - Agoraphobia
Purpose:   This study will evaluate the effectiveness of intensive cognitive behavioral therapy in treating adolescents with panic disorder with agoraphobia.
Study Summary:   Panic disorder (PD) in adolescents is a prevalent and chronic anxiety disorder. People with PD experience unexpected attacks of fear, along with elevated heart rate, dizziness, faintness, weakness, and increased sweating. During these panic attacks, people may feel numbness in their hands, flushed or chilled, nauseous, or pain in the chest, and they may lose touch with reality. PD can lead to substantial social impairment for adolescents, including avoidance of school, independent activities, and peer involvement. When PD progresses so far that a person avoids public places where a panic attack might occur, the person is said to have a condition known as agoraphobia. Weekly sessions of cognitive behavioral therapy (CBT) appear to be effective in treating panic disorder with agoraphobia (PDA). However, many adolescents with PDA and their families report the need for a more immediate relief from the disorder. This study will evaluate the effectiveness of intensive CBT in treating adolescents with PDA. Participants in this single blind study will be randomly assigned to one of three conditions: intensive CBT treatment including family members, intensive CBT treatment without family members, or a waitlist control group. All participants in the intensive CBT treatment groups will undergo 8 days of intensive CBT, for a total of 6 sessions. On Days 1 through 3 of treatment, participants will attend daily, 2-hour CBT sessions. The CBT sessions will include psychoeducation about anxiety, tactics to restructure anxiety-provoking thoughts, and exposure to bodily sensations that trigger panic. On Days 4 and 5, participants will meet with a therapist to learn ways to approach previously feared situations. On Days 6 and 7, participants will continue working independently or with family members to solidify skills. On Day 8, participants will attend a final 2-hour session to consolidate skills, review the independent weekend activities, and discuss ways to apply skills to the home environment. Parents of participants in the parental involvement group will attend the last 30 minutes of sessions, complete homework assignments, learn ways to coach their children through episodes, and participate in selected exposures. After 6 weeks of waitlist, participants in the waitlist control group will receive active treatment following the same procedures as the initial active treatment. All participants will be assessed at Months 3, 6, and 12 post-treatment.
Criteria:   Inclusion Criteria: - Meets DSM-IV criteria for principal diagnosis of PD or PDA prior to treatment - Adolescent must be accompanied by at least one parent or caregiver - If on medication, there must be a 1-month stabilization period for benzodiazepines or 3-month stabilization period for SSRIs or tricyclics prior to study entry Exclusion Criteria: - Positive diagnosis of schizophrenia, pervasive developmental disorder, organic brain syndrome, mental retardation, or current suicidal ideation - Unavailability of at least one parent or caregiver - Refusal of parent to accept random assignment to treatment condition - Refusal of parent or adolescent to accept stabilization of medication - Adolescent with parent who has any condition that would limit ability to understand treatment
NCT ID:   NCT00576719
Primary Contact:   Principal Investigator
Donna Pincus, PhD
Boston University

Sarah Whitton, PhD
Phone: 617-353-9610
Email: panic@bu.edu
Backup Contact:   N/A
Location Contact:   Boston, Massachusetts 02215
United States



There is no listed contact information for this specific location.

Site Status: Recruiting

Data Source:   ClinicalTrials.gov
Date Processed:   May 19, 2013
Modifications to this listing:   Only selected fields are shown, please use the link below to view all information about this clinical trial.
Click to view Full Listing


If you would like to be contacted by the clinical trial representative please enter your contact information, then click "I Am Interested In This Study"
First Name:  
Last Name:  
Email Address:  
Confirm Email:    
Daytime Phone (eg. 555-555-5555):  
City:  
State:
Zip Code:    
Best Time to Call:  
Questions/Comments:  
  • NEARBY STUDIES

Within 25 Miles

Tai Chi and Aerobic Exercise for Fibromyalgia - Boston MA

Crohn's Disease - Brockton MA

Osteoarthritis - Boston MA

Irritable Bowel Syndrome with Diarrhea (IBS-D) - Brockton MA

Gingivitis - Cambridge MA

Gum Disease - Cambridge MA

Excessive Daytime Sleepiness with Narcolepsy - Newton Center MA

Irritable Bowel Syndrome (with diarrhea) - Watertown MA

Postherpetic Neuralgia (Post-shingles pain) - Roslindale MA

Crohn's Disease - Quincy MA

Cataracts - Quincy MA

Chronic Low Back Pain - Watertown MA

Healthy Volunteers (Weighing less than 175 lbs) - Boston MA

Carbohydrates - Boston MA

Healthy Volunteers (Weighing more than 175 lbs) - Boston MA

Multiple Sclerosis - Brookline MA

Chronic Lower Back Pain - Brockton MA

Diabetic Neuropathy - Brockton MA

Constipation - Brockton MA

Fibromyalgia - Brockton MA

Osteoarthritis - Brockton MA

Constipation with Chronic Lower Back Pain - Brockton MA

High Cholesterol - Brockton MA

Gout with Heart Conditions - Brockton MA

Irritable Bowel Syndrome - Brockton MA

Low Back Pain and Constipation - Brockton MA

Anti-Depressant Induced Sexual Dysfunction - Brighton MA

Anti-Depressant Induced Sexual Dysfunction - South Weymouth MA

Irritable Bowel Syndrome (with diarrhea) - Brockton MA

Obsessive Compulsive Disorder (OCD) - Boston MA

Post Herpatic Neuralgia - Brockton MA

Chronic Lower Back Pain and Constipation - Brockton MA

Uncontrolled Angina (Adult Stem Cell Research) - Boston MA

Rosacea - Brockton MA

Within 50 Miles

Alzheimer's Disease - East Providence RI

Crohn's Disease - Worcester MA

Restless Legs Syndrome (RLS) - Warwick RI

Irritable Bowel Syndrome (with diarrhea) - Cumberland RI

Multiple Sclerosis - Providence RI

Asthma (Ages 18-65) - Warwick RI

Gout - Worcester MA

Low Back Pain and Constipation - Fall River MA

Low Back Pain and Constipation - Warwick RI

Arthritis - Fall River MA

Irritable Bowel Syndrome (with diarrhea) - East Providence RI

Postherpetic Neuralgia (Post-shingles pain) - New Bedford MA

Osteoarthritis - New Bedford MA

Obsessive Compulsive Disorder (OCD) - Providence RI

COPD (Emphysema and Chronic Bronchitis) - Fall River MA

Within 100 Miles

Arthritis - New London CT

Fibromyalgia - New London CT

Arthritis - Biddeford ME

Anti-Depressant Induced Sexual Dysfunction - Norwich CT

 
Clinical Connections Home | Investigators | CROs / Sponsors | Clinical Trials Notification | Search Clinical Trials | About Clinical Trials | Links | Terms And Conditions | Sitemap | Suggestions / Feedback
© 1998-2013 | All trademarks are property of their legal owners. | All Rights Reserved

ClinicalConnection.com is a resource that provides individuals with information regarding clinical trials that are being conducted worldwide.

ClinicalConnection.com does not conduct these clinical trials nor endorse them. Please consult your doctor or physician before participating.