TY - JOUR
T1 - The Treatment for Adolescents with Depression Study (TADS)
T2 - Demographic and clinical characteristics
AU - March, John
AU - Silva, Susan
AU - Petrycki, Stephen
AU - Curry, John
AU - Wells, Karen
AU - Fairbank, John
AU - Burns, Barbara
AU - Domino, Marisa
AU - McNulty, Steven
AU - Vitiello, Benedetto
AU - Severe, Joanne
AU - Casat, Charles
AU - Kolker, Jeanette
AU - Riedal, Karyn
AU - Goldman, Marguerita
AU - Feeny, Norah
AU - Findling, Robert
AU - Stull, Sheridan
AU - McNamara, Nora
AU - Weller, Elizabeth
AU - Robins, Michele
AU - Weller, Ronald
AU - Jessani, Naushad
AU - Waslick, Bruce
AU - Sweeney, Michael
AU - Kandel, Rachel
AU - Schoenholz, Dena
AU - Walkup, John
AU - Ginsburg, Golda
AU - Kastelic, Elizabeth
AU - Koo, Hyung
AU - Kratochvil, Christopher
AU - May, Diane
AU - LaGrone, Randy
AU - Harrington, Martin
AU - Albano, Anne Marie
AU - Hirsch, Glenn
AU - Knibbs, Tracey
AU - Capili, Emlyn
AU - Reinecke, Mark
AU - Leventhal, Bennett
AU - Nageotte, Catherine
AU - Rogers, Gregory
AU - Pathak, Sanjeev
AU - Wells, Jennifer
AU - Arszman, Sarah
AU - Danielyan, Arman
AU - Simons, Anne
AU - Rohde, Paul
AU - Grimm, James
AU - Nguyen, Lananh
AU - Emslie, Graham
AU - Kennard, Beth
AU - Hughes, Carroll
AU - Ruberu, Maryse
AU - Rosenberg, David
AU - Benazon, Nili
AU - Butkus, Michael
AU - Bartoi, Marla
AU - Clarke, Greg
AU - Brent, David
AU - Koch, Gary
N1 - Funding Information:
Disclosure: John March is a speaker for Pfizer and Eli Lilly and receives research support from Eli Lilly, Pfizer, and Wyeth. Charles Casat has research contracts with Eli Lilly, GlaxoSmithKline, Shire, Bristol-Myers Squibb, AstraZeneca, Sanofi Synthelabo, Pfizer, and McNeil; is on the Advisory Board and the Speaker Bureau of Eli Lilly and GlaxoSmithKline. Robert Findling receives research support from Abbott, AstraZeneca, Best Practices, Bristol-Myers Squibb, Celltech-Medeva, Forest, GlaxoSmithKline, Johnson and Johnson, Layton Biosciences, Eli Lilly, Nature's Herbs, Novartis, Organon, Otsuka, Pfizer, Shire, Solvay, Somerset, and Wyeth; is a consultant for Abbott, AstraZeneca, Best Practices, Bristol-Myers Squibb, Celltech-Medeva, Forest, GlaxoSmithKline, Johnson and Johnson, Eli Lilly, Novartis, Noven, Otsuka, Pfizer, Shire, Somerset, and Wyeth; and is on the Speaker's Bureau of Abbott, AstraZeneca, Bristol-Myers Squibb, GlaxoSmithKline, Johnson and Johnson, Eli Lilly, Otsuka, Shire, and Wyeth. Elizabeth Weller is a consultant for and receives grants from Otsuka, Johnson and Johnson, AstraZeneca, Organon, Pharma, Shire, and GlaxoSmithKline. Bruce Waslick receives research support from Eli Lilly. John Walkup receives research support and honoraria from Eli Lilly. Golda Ginsburg receives research support from Pfizer. Elizabeth Kastelic receives an honorarium from Pfizer. Christopher Kratochvil receives research support from Eli Lilly, Forest, and GlaxoSmithKline and is a consultant for and on the Speaker's Bureau of Eli Lilly. Martin Harrington has affiliations or financial involvement with Eli Lilly, Pfizer, and AstraZeneca. Bennett Leventhal is a consultant and speaker for Eli Lilly and receives research support from Eli Lilly. James Grimm receives research support from GlaxoSmithKline, Sepracor, Shire, Ortho-McNeil, AstraZeneca, Organon, Forest, and Cephalon. Graham Emslie receives research support from Eli Lilly, Organon, RepliGen, and Wyeth-Ayerst; is a consultant for Eli Lilly, GlaxoSmithKline, Forest Laboratories, and Pfizer; and is on the Speaker's Bureau for McNeil. The other authors have no financial relationships to disclose.
PY - 2005/1
Y1 - 2005/1
N2 - Objective: The Treatment for Adolescents With Depression Study is a multicenter, randomized clinical trial sponsored by the NIMH. This study is designed to evaluate the short- and long-term effectiveness of four treatments for adolescents with major depressive disorder: fluoxetine, cognitive-behavioral therapy, their combination, and, acutely, pill placebo. This report describes the demographic and clinical characteristics of the sample and addresses external validity. Method: Participants are 439 adolescents, aged 12-17 years inclusively, with a primary DSM-IV diagnosis of current major depressive disorder. Baseline data are summarized and compared with those from national samples and previous trials. Results: The sample composition is 54.4% girls, 73.8% white, 12.5% African American, and 8.9% Hispanic. The mean Child Depression Rating Scale-Revised total score is 60.1 (SD = 10.4, range 45-98) with 86.0% experiencing their first major depressive episode. The most common concurrent diagnoses are generalized anxiety disorder (15.3%), attention-deficit/hyperactivity disorder (13.7%), oppositional defiant disorder (13.2%), social phobia (10.7%), and dysthymia (10.5%). Demographic results are consistent with data from national samples and large psychopharmacology trials involving depressed adolescents. Conclusions: The Treatment for Adolescents With Depression Study provides a large, diverse, and representative sample of depressed adolescents that highlights the complexity of major depressive disorder in adolescents and provides a rich source for explicating the effects of moderator and mediator variables on baseline psychopathology and treatment outcome.
AB - Objective: The Treatment for Adolescents With Depression Study is a multicenter, randomized clinical trial sponsored by the NIMH. This study is designed to evaluate the short- and long-term effectiveness of four treatments for adolescents with major depressive disorder: fluoxetine, cognitive-behavioral therapy, their combination, and, acutely, pill placebo. This report describes the demographic and clinical characteristics of the sample and addresses external validity. Method: Participants are 439 adolescents, aged 12-17 years inclusively, with a primary DSM-IV diagnosis of current major depressive disorder. Baseline data are summarized and compared with those from national samples and previous trials. Results: The sample composition is 54.4% girls, 73.8% white, 12.5% African American, and 8.9% Hispanic. The mean Child Depression Rating Scale-Revised total score is 60.1 (SD = 10.4, range 45-98) with 86.0% experiencing their first major depressive episode. The most common concurrent diagnoses are generalized anxiety disorder (15.3%), attention-deficit/hyperactivity disorder (13.7%), oppositional defiant disorder (13.2%), social phobia (10.7%), and dysthymia (10.5%). Demographic results are consistent with data from national samples and large psychopharmacology trials involving depressed adolescents. Conclusions: The Treatment for Adolescents With Depression Study provides a large, diverse, and representative sample of depressed adolescents that highlights the complexity of major depressive disorder in adolescents and provides a rich source for explicating the effects of moderator and mediator variables on baseline psychopathology and treatment outcome.
KW - Adolescence
KW - Controlled trials
KW - Depression
KW - Phenomenology
KW - Randomized
KW - Treatment
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UR - http://www.scopus.com/inward/citedby.url?scp=19944363159&partnerID=8YFLogxK
U2 - 10.1097/01.chi.0000145807.09027.82
DO - 10.1097/01.chi.0000145807.09027.82
M3 - Article
C2 - 15608541
AN - SCOPUS:19944363159
SN - 0890-8567
VL - 44
SP - 28
EP - 40
JO - Journal of the American Academy of Child and Adolescent Psychiatry
JF - Journal of the American Academy of Child and Adolescent Psychiatry
IS - 1
ER -