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Depressive Disorder clinical trials

View clinical trials related to Depressive Disorder.

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NCT ID: NCT01805440 Completed - Bipolar Disorder Clinical Trials

Uridine Adolescent Bipolar Depression Randomized Controlled Trial

Start date: August 2013
Phase: N/A
Study type: Interventional

This is a randomized, double-blind, placebo-controlled study of the investigational drug uridine as a treatment for depressed adolescents with bipolar disorder (i.e. "bipolar depression"). Participants initially randomized to placebo who complete the 6-week protocol will be offered 6 months of open-label uridine treatment and follow-up. Participants initially randomized to uridine will be offered the open-label treatment as well.

NCT ID: NCT01803802 Completed - Clinical trials for Major Depressive Disorder

Effects of Early Abuse on Adult Intimate Relationships

Start date: April 2005
Phase: N/A
Study type: Interventional

This study is designed to help us better understand the factors that affect the sexual lives of women who have been sexually mistreated during childhood. With this study we hope to learn about factors that may be promising targets for future treatments of sexual problems related to past sexual experiences. The investigators hypothesize that women who have experienced early sexual abuse are more likely to have sexual problems in adulthood than women who were not abuse in childhood.

NCT ID: NCT01802437 Completed - Clinical trials for Adolescent Depression

An Adaptive Treatment Strategy for Adolescent Depression

PTAD
Start date: November 2010
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of the study is: 1. to find out how long teenagers getting talk therapy (interpersonal psychotherapy) for depression should get therapy before the therapist decides whether or not the teenager is improving enough, and 2. to compare two ways of providing treatment to teenagers who have not improved enough.

NCT ID: NCT01799551 Completed - Depression Clinical Trials

Brief Culturally Adapted Cognitive Behaviour Therapy for Depression

Start date: November 2012
Phase: N/A
Study type: Interventional

Cognitive behaviour therapy (CBT) has an effective evidence base in the west and is recommended by the national bodies in many countries in the West. Our group has adapted CBT for depression and psychosis in Pakistan for use with local clients. Initial evaluations have found that these therapies are effective. However, due to the financial restraints it would be useful if the investigators find that brief version of the CBT might be applicable and effective in non western cultures. Therefore in this study, the investigators will be testing effectiveness of brief version of culturally adapted CBT for depression in a randomized controlled trial (RCT) in Pakistan.

NCT ID: NCT01795326 Completed - Schizophrenia Clinical Trials

Physician Survey on Monitoring of Patients Treated With Quetiapine

Start date: June 2013
Phase: N/A
Study type: Observational

A physician survey to document receipt of metabolic educational materials and assess behavior of physicians in following messages communicated through the educational materials

NCT ID: NCT01793324 Completed - Schizophrenia Clinical Trials

EMR Data to Assess Monitoring of Patients Treated With Quetiapine

Start date: April 2012
Phase: N/A
Study type: Observational

A study to evaluate the effectiveness of an update of educational materials with respect to evaluation of monitoring of metabolic parameters

NCT ID: NCT01792414 Completed - Major Depression Clinical Trials

Transcranial Electrical Stimulation (TES) for the Treatment of Depression.

Start date: January 2013
Phase: N/A
Study type: Interventional

This study is a RCT of transcranial electrical stimulation in depressed patients. Mood, cognitive test performance and biomarkers will be measured during the trial.

NCT ID: NCT01791023 Completed - Depression Clinical Trials

Stress Reactivity of Physical Stressor on Depression

Start date: March 2011
Phase: N/A
Study type: Interventional

Depressive elderly individuals have showed higher basal level of cortisol and lower level of dehydroepiandrosterone (DHEA). Moreover, changes on these hormone levels have also observed in reactivity of an acute stress, such as physical exercise. On the other hand, physical training can modulate the release of these hormones. Therefore, depressive elderly individuals physically actives might show attenuated reactivity of an acute physical stressor compared to sedentary elderly individuals. The aim of these study is to compare the effect of an acute physical stressor on cortisol levels in depressive and healthy individuals, physically actives and sedentaries. Additionally, the sulfated form of DHEA (DHEAS) serves as a reservoir for DHEA, because of that it is expected that DHEAS levels might reduce after the acute physical exercise.

NCT ID: NCT01790919 Completed - Clinical trials for Major Depressive Disorder (MDD)

Improving Depression Outcome by Enhancing Memory for Cognitive Therapy

Start date: February 2013
Phase: Phase 2
Study type: Interventional

Existing drug and talking therapies for major depressive disorder (MDD) fail to produce complete recovery. This study will determine if substantial improvements to one of the most promising therapies, cognitive therapy (CT), can be achieved by administering a carefully designed procedure to improve memory for the content of CT sessions. This is important because (a) memory deficits are common in MDD patients and (b) each CT therapy session typically covers a complex array of topics and various skills are taught.

NCT ID: NCT01788657 Completed - Major Depression Clinical Trials

iCBT for Depression - Standard Versus Condensed Treatment Material

KONRAD
Start date: October 29, 2013
Phase: N/A
Study type: Interventional

Internet-based cognitive behavior therapy (iCBT) has been shown effective for depression in several studies, however the investigators know very little about how the written treatment material should be designed to be effective and at the same time acceptable to the patients. The investigators are not aware of any research that has investigated if slow readers, or persons with difficulty concentrating, can use the standard material or if they would benefit more from using an adapted version. In this study the investigators will assess reading speed and the ability to concentrate in all patients and then randomise them to an internet-based treatment for depression using either a standard material or a condensed one. The condensed material consists of 30000 words and will be available as text files and on audio files. The standard material consists of 60000 words and is only available as text files. Both groups will have the possibility of e-mail contact with a personal therapist during the treatment. Patients will be recruited within Örebro County by referrals and self-referrals. The goal is to recruit between 200 and 300 patients during 2 years. The treatment time will be 10 weeks and all patients will be assessed for depression at an interview with a psychologist. There will also be interviews after treatment and one year after treatment. The most important outcome will be depressive symptoms.