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Hypokinesia clinical trials

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NCT ID: NCT02968342 Recruiting - Menopause Clinical Trials

Role of Progesterone in Hypoactive Sexual Desire Disorder in Menopausal Women

Start date: July 2016
Phase: Phase 4
Study type: Interventional

The objective of this study is the role of vaginal progesterone gel in the treatment of menopausal hypoactive sexual desire disorder. Half of the study participants will receive a standard dose of self applied vaginal progesterone gel and the other half will receive oral vitamin tablets.

NCT ID: NCT02899156 Terminated - Hypoactive Delirium Clinical Trials

Flumazenil for Hypoactive Delirium Secondary to Benzodiazepine Exposure

FLYP
Start date: March 2016
Phase: Phase 4
Study type: Interventional

Delirium within the intensive care unit (ICU) is associated with poor outcomes such as increased mortality, ICU and hospital length of stay (LOS), and time on mechanical ventilation. Benzodiazepine (BZD) exposure is an independent risk factor for development of delirium. Reversal of hypoactive delirium represents a potential opportunity for reducing duration of delirium and subsequent complications. This is a single-center randomized, double-blind, placebo-controlled study of critically ill adult patients with benzodiazepine-associated hypoactive delirium. The hypothesis is that flumazenil continuous infusion may reverse hypoactive delirium associated with BZD exposure and thereby reduce duration of delirium and ICU LOS.

NCT ID: NCT02770768 Terminated - Clinical trials for Hypoactive Sexual Desire Disorder

Effects of Flibanserin on the Pre- and Post-menopausal Female Brain

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

The purpose of the present study is to understand the neurobiological mechanisms of action underlying sexual desire building on prior work Dr. Stephanie Cacioppo has done in which desire was not manipulated. In the present project, Dr. Stephanie Cacioppo is manipulating desire through Flibanserin (Addyi) vs. placebo and she will be measuring subjective sexual desire as a manipulation check. The investigators will address this goal using a double-blind randomized outpatient design and determine the pre-post neurobehavioral change in the Flibanserin group and investigate the extent to which Flibanserin normalizes brain activity in premenopausal women with HSDD and the extent to which regional brain activation is associated with changes in symptoms and behavior (as measured with self-report measures of sexual desire and/or eye-tracking movements).

NCT ID: NCT02714049 Terminated - Clinical trials for Hypoactive Sexual Desire Disorder

Flibanserin (Addyi®) vs. Flibanserin and Sex Therapy

Start date: January 25, 2017
Phase: Phase 4
Study type: Interventional

Unblinded study of flibanserin for 8 weeks with responders randomized 1:1 to receive study medication alone vs. study medication and sex therapy for 12 additional weeks.

NCT ID: NCT02601534 Completed - Hypokinesia Clinical Trials

Be Healthy, So Easy: FAMILY Education Project

Start date: July 2015
Phase: N/A
Study type: Interventional

The goal of the study is to evaluate the effectiveness of a family-focused, interactive, and theory-based intervention to reduce the sedentary behavior and increase physical activity, family communication and well-being of the participants. The intervention is to use Zero-time Exercise, the positive psychology theme "Appreciation and Gratitude" [23, 24], and role modelling approach to get sedentary people to start exercising, increase levels of physical activity, family communication and well-being of the participants and their family members. The intervention aims to encourage positive and sustainable health actions among participants and their family members.

NCT ID: NCT02593396 Completed - Clinical trials for Hypoactive Sexual Desire Disorder

Bupropion in Sexual Dysfunction Among Methadone Maintenance Treatment Men

Start date: December 2015
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess the tolerability, safety, and efficacy of bupropion hydrochloride sustained-release in the treatment of sexual dysfunction in men on methadone maintenance therapy.

NCT ID: NCT02506205 Recruiting - Clinical trials for Hypokinetic Dysathria

The Effect of LSVT LOUD for Mandarin-speaking Individuals With Hypokinetic Dysarthria Due to Parkinson's Disease

Start date: October 2014
Phase: N/A
Study type: Interventional

A handful of studies have examined the effects of the Lee Silverman Voice Treatment (LSVT) LOUD on hypokinetic dysarthria in English speakers with Parkinson's disease (PD). Although LSVT LOUD has been found to be effective on improving these speaker's vocal intensity and increasing their speech intelligibility as well as speech function with Phase I evidence, no study has investigated whether Mandarin-speaking individuals with dysarthria secondary to PD would benefit from LSVT LOUD. In the proposed study, speech data of Mandarin-speaking individuals with hypokinetic dysarthria before and after speech therapy will be audio recorded and analyzed in order to examine the effects of LSVT LOUD on the speech function in this population. The same speech data will be played to Mandarin listeners in order to investigate the speech intelligibility of this population. It is hypothesized that Mandarin-speaking individuals with hypokinetic dysarthria secondary to PD will demonstrate reduced vocal intensity, reduced speech intelligibility and impaired speech function before they receive LSVT LOUD. They will improve these speech characteristics following speech therapy and will present with short-term maintenance effects.

NCT ID: NCT02430987 Completed - Obesity Clinical Trials

Low Sexual Desire and Metabolic Syndrome

Start date: September 2014
Phase: N/A
Study type: Interventional

Objective: To evaluate the prevalence of hypoactive sexual desire disorder (HSDD) in postmenopausal women diagnosed with metabolic syndrome (MS) and to compare it to that of a control group without MS. Design: Cross-sectional study. Setting: Two public tertiary hospitals in the state of São Paulo, Brazil. Population: Two-hundred ninety-one postmenopausal women between 40 and 65 years of age. Methods: Sexual function was evaluated using the Female Sexual Function Index (FSFI) questionnaire and DSM-IV-TR diagnostic criteria and was related to the diagnosis of MS, which was determined according to the guidelines defined by the Adult Treatment Panel (ATP III). Main outcome measures: Analysis of sexual function with emphasis on sexual desire (HSDD), the presence of MS and its components.

NCT ID: NCT02419209 Completed - Clinical trials for Hypoactive Sexual Desire Disorder

The Effect of Individualised Homeopathic Treatment on Low Sexual Desire in Perimenopause

Start date: January 2015
Phase: Phase 2
Study type: Interventional

Low sexual desire, or decreased libido, is one of the most prevalent sexual complaints in females. Menopause is defined as the physiologic cessation of menses brought on by a decrease in ovarian function and is established once menses have been absent for at least twelve months. Perimenopause refers to the period shortly before as well as the twelve months after the last menstrual period. The duration of perimenopause varies greatly and signs and symptoms usually begin appearing during a woman's forties. A longitudinal study conducted in Seattle showed that women experienced a significant reduction in sexual desire during the late perimenopausal and early postmenopausal stages, with the biggest decline in sexual desire occurring from three years prior to two years after the final menstrual period. Despite being a prevalent female complaint, currently no standard treatment for low sexual desire exists. Homeopathy may offer a safe and effective solution for this common problem, however limited research has been conducted to date. The aim of this study is to explore the effect of individualised homeopathic treatment on low sexual desire in perimenopausal females using detailed case studies, the desire and arousal subscales of the Female Sexual Function Index (FSFI) as well as Item 13 of the Female Sexual Distress Scale - Revised (FSDS-R).

NCT ID: NCT02345902 Recruiting - Hypoactive Delirium Clinical Trials

Treatment of Hypoactive Delirium and Outcome Measures

THDOM
Start date: January 2016
Phase: Phase 3
Study type: Interventional

Haloperidol and Non-Pharmacologic Treatment are recognized treatments for delirium. This study will evaluate which is the best treatment for hypoactive delirium.