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NCT ID: NCT02029365 Terminated - Infertility Clinical Trials

Transversal, Controlled and Not Randomized Study, Laying on the Desire of Children and Eating Disorders in a Population of Infertile Women

TCA2
Start date: January 2014
Phase: N/A
Study type: Interventional

In France , 15% of couples seek help for problems conceiving . In 10% of cases, infertility remains " unexplained" . Among the causes of female infertility , there are the eating disorders, as well as sexual disorders , these two cases may be linked. In addition, data from the literature seem to suggest that beyond a diagnosis of eating disorders, the feeding behavior of infertile women is more often disturbed than the general population. Moreover, the notions of desire for a child and maternal representations seem essential to address in the comprehensive care of women with infertility but also TCA integrating all conflicting issues reactivated at the time of motherhood. However, little work has been done on this subject. Thus, we propose a study on the desire for children and the eating disorders to infertile women, to update epidemiological data, but also to better characterize this particular patient population. Perspectives of this work are to improve screening measures and support through a joint work of doctors reproductive and psychiatrists.

NCT ID: NCT02007447 Terminated - Clinical trials for Autism Spectrum Disorder

Oxytocin in Adolescents With Autism Spectrum Disorders

OXYASD
Start date: June 2015
Phase: Phase 2/Phase 3
Study type: Interventional

This study is design to evaluate the influence of oxytocin in some aspects of Autism Spectrum Disorder (ASD), such as, repetitive and stereotyped behavior, social skills, quality of life and disruptive behaviors. Null hypothesis: social skills, quality of life, disruptive behaviors and repetitive behaviors do not improve with the use of oxytocin. Experimental Hypothesis: social skills, quality of life, disruptive behaviors and repetitive and stereotyped behaviors improve with the use of oxytocin.

NCT ID: NCT01983189 Terminated - Autism Clinical Trials

Transcranial Magnetic Stimulation for Evaluation and Treatment of Repetetive Behaviors in Autism

Start date: November 2008
Phase: Phase 2
Study type: Interventional

This study is a trial of low frequency Repetitive Transcranial magnetic stimulation( rTMS) for subjects with autism spectrum disorders, specially targeting repetitive behaviors.

NCT ID: NCT01979263 Terminated - Clinical trials for Obsessive-Compulsive Disorder

Attention Bias Modification Treatment for Anxious Youth

ABMT
Start date: October 2013
Phase: N/A
Study type: Interventional

The purpose of this project is to study the feasibility and efficacy of attention bias modification treatment (ABMT) in a randomized-controlled sample of anxious youth.

NCT ID: NCT01957501 Terminated - Clinical trials for Major Depressive Disorder

Detecting Depression and Bipolar Disorder in Adolescents Using a Biomarker Panel

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

Depression and bipolar disorder are major public health concerns for adolescents today. Teenage depression and bipolar disorder are associated with social isolation, family stress, school failure, substance abuse and suicide. Screening for depression and bipolar disorder so that treatment can be started early in the course of illness is an urgent public health priority. Many teens with bipolar disorder are incorrectly diagnosed as having unipolar depression. It is critical that adolescents receive proper screening and assessment that leads to an accurate diagnosis and treatment. An efficient, cost-effective, blood-based screening program could be performed on an annual or semi-annual basis to potentially detect depression and then differentiate between unipolar and bipolar depression. If this type of screening were able to detect a significant percentage of teens with depression or bipolar disorder, the positive impact on U.S. public health would be substantial. The purpose of this study is to conduct a pilot study to assess the probability of detecting adolescent unipolar and bipolar depression through blood samples.

NCT ID: NCT01948427 Terminated - Urea Cycle Disorder Clinical Trials

Observational Study That Will Collect Information on Patients With Urea Cycle Disorders (UCDs)

THRIVE
Start date: September 25, 2013
Phase:
Study type: Observational [Patient Registry]

THRIVE is an observational study that will collect information on patients with UCDs. THRIVE will follow enrolled participants for up to 10 years. As an observational study, enrolled patients will not be required to make any additional office visits or take any medicine outside of normal care.

NCT ID: NCT01944969 Terminated - Clinical trials for Major Depressive Disorder

Long-term Safety and Tolerability Study of Brexpiprazole as Adjunctive Treatment in Patients With Major Depressive Disorder

Start date: October 2013
Phase: Phase 3
Study type: Interventional

To evaluate the long-term safety and tolerability of brexpiprazole as adjunctive treatment in patients with Major Depressive Disorder (MDD)

NCT ID: NCT01928264 Terminated - Depressive Disorder Clinical Trials

Physical Activity in Insurance Medicine: Effects on Patients With Psychiatric Disorders

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

We will conduct a randomized control trial to investigate whether and to what extent regular and guided group physical activity over 12 weeks (2 sessions à 1 hour/week) improves physical fitness and (physio-)psychological functions (like subjective sleep, mental toughness, perceived stress, self-efficacy, etc.), as well as participation skills and the ability to work, in claimants for a disability pension due to psychiatric disorders, whose ability to work had recently been assessed by means of a psychiatric expert opinion. The control group is designed very similar and implies predominantly sedentary leisure time group activities (e.g. playing board games, doing handicrafts). Measures will be performed at baseline, post-test, and at follow ups three and twelve months after post-test, some variables will additionally be assessed 4-weekly during the intervention. We expect that intervention group participants will report and show, respectively, more improved physical fitness, (physio-)psychological functioning and participations skills, as well as increased ability to work, compared to the control group.

NCT ID: NCT01928043 Terminated - Bipolar Disorder Clinical Trials

Adjunctive Curcumin for Symptomatic Adolescents With Bipolar Disorder: Brain and Body Considerations

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

This study will enroll 30 adolescents with bipolar disorder (BD) who are suffering from symptoms of depression despite already taking a traditional mood-stabilizing medication. Curcumin will be added to their current medications for 8 weeks. During these 8 weeks, their mood symptoms will be assessed regularly. Height, weight, and blood pressure will also be measured repeatedly. Blood tests will be completed before treatment, after 4 weeks of treatment, and at the end of the study. Blood tests will allow us to determine whether changes in inflammation and oxidative stress explain curcumin's effect on mood. Finally, we will use sophisticated technology to measure blood vessel functioning. We have three main predictions: 1. Curcumin will improve mood symptoms without causing physical problems; 2. Curcumin will reduce inflammation and oxidative stress, and these reductions will be linked to improvements in mood; 3. Curcumin will improve blood vessel functioning, and these improvements will be linked to improved inflammation and oxidative stress.

NCT ID: NCT01917318 Terminated - Clinical trials for Post Traumatic Stress Disorder

Iloperidone for Symptoms of Arousal in Post Traumatic Stress Disorder (PTSD)

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

A Double-Blind Placebo-Controlled Random Order Crossover Pilot Study of Iloperidone for Symptoms of Arousal in PTSD.