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Hypokinesia clinical trials

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NCT ID: NCT03780751 Completed - Clinical trials for Hypoactive Sexual Desire Disorder

Waitlist Controlled Comparison of Cognitive-behavioral vs. Mindfulness-based Online-treatments for Women With Low Sexual Desire

MiSELF
Start date: December 18, 2018
Phase: N/A
Study type: Interventional

Problems with sexual function are common and distressing. The most frequent sexual difficulty in women is a lack of sexual desire with a prevalence of 20-30%. When low sexual desire is experienced over several months and causes significant personal distress, a sexual dysfunction can be diagnosed (ICD-10: Hypoactive Sexual Desire Disorder: HSDD). A distressing lack of desire is reported by 6% of sexually active women. Psychological interventions are the treatment of choice for women with HSDD. Promising treatment approaches include cognitive-behavioral and mindfulness-based interventions. A recent meta-analysis also showed that Internet-delivered programs are a valid alternative to face-to-face treatments. Aim of this project to assess the effectivity of two eight-week online-programs consisting of cognitive-behavioral (COPE) and mindfulness-based (MIND) interventions for women with HSDD. Both treatments will be compared to a waitlist-control group. For this project, two well-established group-treatment manuals will be translated into German and adapted to a multimedia online-environment. All participants will be guided through the programs by well-qualified eCoaches.

NCT ID: NCT03613324 Completed - Clinical trials for Bladder Outlet Obstruction and Detrusor Underactivity in Women With Severe Cystocele

BOO and DU and Their Clinical and Urodynamic Findings in Women With ≥Stage II Cystocele

Start date: January 1, 2011
Phase:
Study type: Observational

Prevalence rates of bladder outlet obstruction (BOO) and detrusor underactivity (DU) and their related clinical and urodynamic findings in women with ≥ pelvic organ prolapse quantification stage II cystocele are important for clinical consultation. Thus, the aim of this study was to elucidate the above findings and between-group associations.

NCT ID: NCT03472898 Completed - Clinical trials for Cardiovascular Diseases

Gated SPECT Abnormality With J Point Elevation

Start date: December 27, 2017
Phase:
Study type: Observational

The investigators present an interesting co-incidence of Gated wall abnormality in the inferolateral wall in normal sestamibi myocardial perfusion images with J wave in the inferior derivations of the ECG in a patient. The subsequent coronary angiography demonstrated 80% mid right coronary artery (RCA) stenosis, which was intervened with a drug-eluting stent. The investigators conclude that even though the myocardial perfusion is normal, the association of gated wall abnormality with J wave presentation within the same location should be further evaluated.

NCT ID: NCT03287232 Completed - Clinical trials for Hypoactive Sexual Desire Disorder

Prasterone (DHEA) for the Treatment of Hypoactive Sexual Desire Disorder (HSDD)

Start date: October 16, 2017
Phase: Phase 3
Study type: Interventional

The primary objective is to confirm the efficacy of intravaginal prasterone (DHEA) on Hypoactive Sexual Desire Disorder (HSDD) in postmenopausal women.

NCT ID: NCT03232801 Completed - Sexual Dysfunction Clinical Trials

A Mindfulness-based Intervention for Older Women With Low Sexual Desire

Start date: October 8, 2020
Phase: N/A
Study type: Interventional

The overall aim of this research is to adapt and pilot test a multi-component, mindfulness-based behavioral intervention for women age 50 and older with low sexual desire.

NCT ID: NCT03175029 Completed - Overactive Bladder Clinical Trials

Exploratory Study of TAC-302 in Detrusor Underactivity Patients With Overactive Bladder.

Start date: August 1, 2017
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of TAC-302 in detrusor underactivity patients with overactive bladder.

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: 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).