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NCT ID: NCT02680899 Completed - Clinical trials for Substance-Related Disorders

Adolescent Mental Health InSciEd Out

Start date: February 2016
Phase: N/A
Study type: Interventional

The study herein seeks to determine whether students undergoing InSciEd Out curriculum in mental health and addiction (called My Mind, My Body) experience changes in their mental health-related knowledge, attitudes, and help-seeking behavioral intentions. The research group hypothesizes that students undergoing InSciEd Out mental health and addiction curriculum will exhibit pre-post increases in mental health literacy, decreases in mental health stigmatization, and increases in mental health help-seeking behavioral intentions.

NCT ID: NCT02678910 Completed - Cancer Clinical Trials

Ovarian Tissue Freezing For Fertility Preservation In Women Facing A Fertility Threatening Medical Diagnosis/Treatment

Start date: February 1, 2017
Phase: N/A
Study type: Interventional

The purpose of this research is to obtain ovarian tissue from female participants who will receive therapy which is expected to result in a loss or impairment of ovarian function and/or infertility and wish to preserve (freeze) ovarian tissue for the purpose of initiating a pregnancy in the future. Removal of the ovary for cryopreservation is an investigational procedure. 100% of the tissue will be used for the participant's future use. There have been 86 pregnancies as a result of frozen ovarian tissue that has been re-implanted back into the pelvis and hormonal function has been restored in individuals for up to 7 years. By doing this study, the investigators hope to learn of how to successfully freeze and thaw ovarian tissue in a manner that permits subsequent use by patients at some point in the future. Participation may also advance our knowledge of how to successfully mature follicles and oocytes (eggs) that are contained in these tissues which may help others in the future.

NCT ID: NCT02676492 Completed - Tic Disorders Clinical Trials

A Naturalistic Study Investigating Sleep and Cognitive Learning in Children With and Without Tic Disorders

Start date: March 2016
Phase: N/A
Study type: Observational

This study will explore the relationship between sleep, learning, cognition, mood and behaviour in children with Tic Disorders (Tourette Syndrome and Chronic Tic Disorder) compared to typically developing peers.

NCT ID: NCT02675712 Completed - Bipolar Disorder Clinical Trials

Effect of African Drumming in Mood Disorders

Start date: April 2015
Phase: N/A
Study type: Observational

This pilot study evaluated whether participating in an African drumming activity for 45 minutes immediately improved mental well-being among 13 adults diagnosed with acute mood disorders who were attending a private mental health clinic. The drumming intervention was completed by occupational therapists.

NCT ID: NCT02673658 Completed - Clinical trials for Motor Coordination or Function; Developmental Disorder

Project for Cognitive Advancement in Infants With Neuromotor Disorders

CAN-Do
Start date: October 2015
Phase: N/A
Study type: Interventional

The purpose of this longitudinal study is to examine the ongoing interaction between the domains of cognitive and motor development in infants with neuromotor disability, and to compare outcomes of two groups of infants receiving two different types of home-based, parent-delivered physical therapy intervention, in order to determine which intervention is more effective in advancing cognitive as well as motor development. Knowledge of the effectiveness of two types of intervention will lead to improved early intervention for children with developmental disabilities, as well as future studies to examine ongoing outcomes.

NCT ID: NCT02671266 Completed - Clinical trials for Obsessive-compulsive Disorder

Oxytocin Administration in BDD and OCD

Start date: December 2014
Phase: Phase 2
Study type: Interventional

The purpose of the current study is to investigate the effect of an acute administration of intranasal oxytocin, relative to placebo, on social cognitive impairments among individuals with body dysmorphic disorder and obsessive-compulsive disorder, compared to healthy controls.

NCT ID: NCT02669901 Completed - Clinical trials for Opioid-Related Disorders

Naloxone Auto-injector as a Universal Precaution for Patients With Opioid Substance Use Disorder

Start date: April 4, 2016
Phase: N/A
Study type: Interventional

The purpose of this pilot-study is to to distribute naloxone auto-injector in a "Universal Precaution" manner to patients with opioid substance use disorder. The objectives are to decrease the number of fatal and nonfatal overdose deaths, to examine and understand the risk factors for serious opioid toxicity and overdose, and to evaluate the unintentional opioid overdose risk utilizing an evidence-based screening questionnaire.

NCT ID: NCT02669082 Completed - Clinical trials for Major Depressive Disorder

The Exploratory Study to Investigate the Effect of Ramelteon for Insomnia Patients With Major Depressive Disorder by Using Actigraphy

Start date: May 9, 2017
Phase: Phase 4
Study type: Interventional

The purpose of this study is to investigate exploratorily the effect of ramelteon 8 mg once daily for 8 weeks in the treatment of insomnia patients with depression by using actigraphy.

NCT ID: NCT02668991 Completed - Clinical trials for Autism Spectrum Disorder

Study to Assess the Janssen Autism Knowledge Engine in Participants With Autism Spectrum Disorder and in a Normally Developing Cohort

Start date: July 2015
Phase: Phase 0
Study type: Observational

The purpose of this study is to evaluate the utility of and to clinically validate the Autism Behavior Inventory (ABI) in measuring clinical symptoms of Autism Spectrum Disorder (ASD) compared with other gold standard measures.

NCT ID: NCT02667119 Completed - Clinical trials for Posttraumatic Stress Disorder

Integrated Treatment for Posttraumatic Stress Disorder and Substance Abuse in Young Adults

Start date: April 2016
Phase: N/A
Study type: Interventional

The purpose of the study is to determine the safety and efficacy of an integrated treatment for substance abuse and posttraumatic stress disorder for young adults. The integrated treatment includes two established psychosocial treatments for substance abuse (Contingency Management) and posttraumatic stress disorder (Prolonged Exposure therapy).