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Adjustment Disorders clinical trials

View clinical trials related to Adjustment Disorders.

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NCT ID: NCT01039857 Terminated - Clinical trials for Adjustment Disorders

Does an Integrative Neuro-psychotherapy Program Foster the Adjustment in Depressed Stroke Patients? A Randomized Controlled Study.

Start date: January 2010
Phase: Phase 1
Study type: Interventional

This is an intervention study with patients after a non-progressive brain injury who suffer from depression. It will determine whether an integration of neuropsychological and psychotherapeutic techniques and an additional caregivers support program offers benefits to those in the process of coping with the effects of a stroke. The investigators expect the integrative neuro-psychotherapy to be more effective in the treatment of emotional distress reactions following a stroke than the structured solution focused treatment.

NCT ID: NCT00883519 Completed - Clinical trials for Major Depressive Disorder

The Efficacy of Parent Involvement in the Treatment of Adolescent Depression

Start date: January 2009
Phase: Phase 1/Phase 2
Study type: Interventional

The primary aim of this study is to examine whether adolescent depression and the family context in which it develops is best treated using an individual adolescent intervention or an intervention that includes both the adolescent and the parents. This will be accomplished by conducting a randomized controlled pilot study of Interpersonal Psychotherapy for Depressed Adolescents (IPT-A) in comparison to Interpersonal Psychotherapy for Depressed Adolescents and Parents (IPT-AP).

NCT ID: NCT00619411 Completed - Major Depression Clinical Trials

Interpersonal Psychotherapy for Depressed Adolescents and Parents

Start date: November 2007
Phase: Phase 1
Study type: Interventional

The purpose of this study is to examine the feasibility and acceptability of an adaptation of Interpersonal Psychotherapy for Depressed Adolescents (IPT-A) that includes greater and more structured involvement of the parents in the treatment.

NCT ID: NCT00555503 Completed - Quality of Life Clinical Trials

Registry of Mastectomy for Breast Cancer Risk Reduction

Start date: November 2007
Phase: N/A
Study type: Observational

This is a registry for patients who have a risk-reduction mastectomy ("prophylactic mastectomy") due to being at high risk for developing breast cancer, followed by breast reconstruction. Eligible patients include those who have a breast cancer-related gene, a strong family history of breast cancer, or a personal history of high-risk conditions such as cancer in the other breast or ductal carcinoma in situ (DCIS). Patients are enrolled in the registry before surgery, and are followed for up to ten years afterwards. In addition to studying medical outcomes, we will periodically survey patients for quality-of-life issues and psychological well-being. There is no compensation for being enrolled in this registry. This registry is conducted through the Department of Plastic Surgery at Georgetown University Hospital, and is a sub-registry to the Fisher Familial Cancer Registry at the Lombardi Comprehensive Cancer Center at Georgetown University.

NCT ID: NCT00399698 Completed - Bipolar Disorder Clinical Trials

Study to Determine Whether There Are Any Cognitive or Motor Effects From Taking the Medicine Risperidone.

Start date: May 1999
Phase: Phase 3
Study type: Interventional

This study was developed in order to assess the effects of risperidone (Risperdal) as compared with placebo on cognitive-motor performance (attention, memory, and hand steadiness) and body movements. We propose to study the effects of risperidone on cognitive-motor performance in children already medicated for severe conduct problems. We would also like to look at safety by assessing these children for dyskinetic movements. We already have a sizable cohort of children maintained on risperidone. Our hypotheses are as follows: 1. Risperidone will have no adverse effects on cognitive-motor performance in children who have received maintenance therapy for 4 to 20 months. 2. Children tested during placebo will show no more dyskinetic movements than during risperidone treatment (i.e., there will be no unmasking of tardive dyskinesia).

NCT ID: NCT00153959 Completed - Schizophrenia Clinical Trials

Psychiatric Day Hospital Treatment

Start date: n/a
Phase: N/A
Study type: Interventional

The aim of the study was to compare the effectiveness of acute psychiatric day care to conventional inpatient care within a cross-national multi-site randomised controlled trial.