Trial record 1 of 1 for:
NCT02828956
Motivation to Change, Coping, and Self-Esteem in Adolescent Anorexia Nervosa
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ClinicalTrials.gov Identifier: NCT02828956 |
Recruitment Status :
Completed
First Posted : July 12, 2016
Last Update Posted : July 12, 2016
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Sponsor:
University of Zurich
Information provided by (Responsible Party):
University of Zurich
Tracking Information | ||||
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First Submitted Date | July 4, 2016 | |||
First Posted Date | July 12, 2016 | |||
Last Update Posted Date | July 12, 2016 | |||
Study Start Date | January 2010 | |||
Actual Primary Completion Date | December 2014 (Final data collection date for primary outcome measure) | |||
Current Primary Outcome Measures |
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Original Primary Outcome Measures | Same as current | |||
Change History | No Changes Posted | |||
Current Secondary Outcome Measures | Not Provided | |||
Original Secondary Outcome Measures | Not Provided | |||
Current Other Pre-specified Outcome Measures | Not Provided | |||
Original Other Pre-specified Outcome Measures | Not Provided | |||
Descriptive Information | ||||
Brief Title | Motivation to Change, Coping, and Self-Esteem in Adolescent Anorexia Nervosa | |||
Official Title | Motivation to Change, Coping, and Self-Esteem in Adolescent Anorexia Nervosa | |||
Brief Summary | By use of several questionaires, this study aimed at an investigation of the changes in motivation, symptoms, self-esteem and coping style in adolescent patients with anorexia nervosa.. The psychometric properties of the Anorexia Nervosa Stages of Change Questionnaire (ANSOCQ) and its relation to coping style and self-esteem were assessed. After a treatment period of nine months, clinical AN diagnosis and the body mass index (BMI) were re-assessed. Besides construct validity of the ANSOCQ, its predictive validity in terms of predicting the outcome of AN was assessed. | |||
Detailed Description | N=92 adolescents referred to an eating disorders clinic meeting criteria for anorexia nervosa (AN) gave written informed consent to participate in this study and completed the ANSOCQ, the Eating Disorder Inventory (EDI-2), the Eating Attitudes Test (EAT), the Body Image Questionnaire (BIQ), two questionnaires measuring Self-Related Cognitions (SRC) and the Coping Across Situations Questionnaire (CASQ). After a treatment period of nine months, clinical AN diagnosis and the body mass index (BMI) were re-assessed. Exploratory factor analysis and logistic regressions were performed. | |||
Study Type | Observational | |||
Study Design | Observational Model: Case-Only Time Perspective: Prospective |
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Target Follow-Up Duration | Not Provided | |||
Biospecimen | Not Provided | |||
Sampling Method | Non-Probability Sample | |||
Study Population | N=92 adolescents referred to our eating disorders clinic meeting criteria for anorexia nervosa (AN). | |||
Condition | Personality Features in Anorexia Nervosa | |||
Intervention | Not Provided | |||
Study Groups/Cohorts | Not Provided | |||
Publications * | Pauli D, Aebi M, Winkler Metzke C, Steinhausen HC. Motivation to change, coping, and self-esteem in adolescent anorexia nervosa: a validation study of the Anorexia Nervosa Stages of Change Questionnaire (ANSOCQ). J Eat Disord. 2017 Apr 17;5:11. doi: 10.1186/s40337-016-0125-z. eCollection 2017. | |||
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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Recruitment Information | ||||
Recruitment Status | Completed | |||
Actual Enrollment |
92 | |||
Original Actual Enrollment | Same as current | |||
Actual Study Completion Date | December 2014 | |||
Actual Primary Completion Date | December 2014 (Final data collection date for primary outcome measure) | |||
Eligibility Criteria | Inclusion Criteria:
Exclusion Criteria:
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Sex/Gender |
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Ages | 12 Years to 19 Years (Child, Adult) | |||
Accepts Healthy Volunteers | No | |||
Contacts | Contact information is only displayed when the study is recruiting subjects | |||
Listed Location Countries | Not Provided | |||
Removed Location Countries | ||||
Administrative Information | ||||
NCT Number | NCT02828956 | |||
Other Study ID Numbers | ANSOCQ_16 | |||
Has Data Monitoring Committee | No | |||
U.S. FDA-regulated Product | Not Provided | |||
IPD Sharing Statement |
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Responsible Party | University of Zurich | |||
Study Sponsor | University of Zurich | |||
Collaborators | Not Provided | |||
Investigators |
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PRS Account | University of Zurich | |||
Verification Date | July 2016 |