Ignite Creation Date:
2024-05-05 @ 11:57 AM
Last Modification Date:
2024-10-26 @ 9:17 AM
Study NCT ID:
NCT00183586
Status:
COMPLETED
Last Update Posted:
2016-06-20
First Post:
2005-09-13
Brief Title:
Comparing the Effectiveness of Three Types of Therapy for the Treatment of Anorexia Nervosa in Adolescents
Sponsor:
University of Chicago
Organization:
University of Chicago
Study Overview
Official Title:
Treatment for Adolescent Anorexia Nervosa
Status:
COMPLETED
Status Verified Date:
2016-06
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This study will compare specific family therapy standard family systems therapy and standard individual psychotherapy to determine which is most effective in treating adolescent anorexia nervosa
Detailed Description:
In adolescents anorexia nervosa severely affects physical emotional and social development Despite the seriousness and prevalence of adolescent anorexia nervosa few studies have focused on the effectiveness of various types of psychotherapy treatment Family-based therapy may be an effective approach to treating adolescent anorexia nervosa This study will compare specific family therapy FT standard family systems therapy FS and standard individual psychotherapy IT to determine which is most effective in treating adolescent anorexia nervosa The study also aims to determine potential predictors and moderators of outcomes as well as the cost-benefit ratio of each treatment
Participants in this open-label study will be randomly assigned to one of three treatment groups Group 1 will receive FT Group 2 will receive FS and Group 3 will receive IT All participants will receive a total of 24 hours of their assigned therapy over a period of 12 months Study visits will occur at baseline immediately post-intervention and again six months and one year post-intervention Weight change will be assessed as well as changes in concerns about weight and shape The cost-benefit ratio of the treatments will also be evaluated
Participants in this open-label study will be randomly assigned to one of three treatment groups Group 1 will receive FT Group 2 will receive FS and Group 3 will receive IT All participants will receive a total of 24 hours of their assigned therapy over a period of 12 months Study visits will occur at baseline immediately post-intervention and again six months and one year post-intervention Weight change will be assessed as well as changes in concerns about weight and shape The cost-benefit ratio of the treatments will also be evaluated
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| DDTR B4-ARE | US NIH GrantContract | None | httpsreporternihgovquickSearchR01MH070620 |
| R01MH070620 | NIH | None | None |