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Quality of Life clinical trials

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NCT ID: NCT02393482 Not yet recruiting - Quality of Life Clinical Trials

Psychological Impact of Amenorrhea in Women With Endometriosis

Start date: June 2021
Phase: Phase 4
Study type: Interventional

The purpose of the study is to evaluate the impact on quality of life, psychological health, sexuality and chronic pain of therapies which determine amenorrhea in symptomatic women with endometriosis, through the administration of self reported questionnaires. Amenorrhea in the first group is caused by balanced assumption of estroprogestins, in the second group is caused by GnRHa-induced hypoestrogenism.

NCT ID: NCT02392923 Completed - Quality of Life Clinical Trials

Quality of Life in a Representative Swedish Population

Normalen
Start date: June 2014
Phase:
Study type: Observational

Cohort descriptive study of quality of life and body functions in a reference population of Swedish inhabitants from age 30 to age 89. The population was selected to be representative for the general Swedish population and 500 in each 10 year group, 250 men and 250 women. The population is contacted and asked for informed consent, whereafter a questionnaire of about 200 questions, used in a number of studies in clinical studies and trials, are sent out. The results will be used as reference values to our patient cohorts

NCT ID: NCT02391818 Completed - Cancer Clinical Trials

The Effect of Taxane Chemotherapy on Balance in Breast Cancer Patients

IPMR Balance
Start date: February 2015
Phase:
Study type: Observational

The purpose of this study is to quantify the balance impairments during and after taxane chemotherapy. Disability due to balance impairments caused by chemotherapy induced peripheral neuropathy (CIPN) can cause falls, injury, and a decline in independence. This results in poor treatment outcomes such as greater morbidity and mortality, inability to complete treatment protocols, self-limitation of activity, and diminished quality of life.

NCT ID: NCT02391766 Enrolling by invitation - Quality of Life Clinical Trials

Group Intervention Empowerment Dementia

Start date: September 2014
Phase: Phase 0
Study type: Interventional

After diagnosis of a dementing illness, patients and their spouses have many concerns related to the disease and their future. This often leads to poor psychological well-being and reduced health-related quality of life (HRQoL) of the family. Support for Empowerment has been proven to be an effective method to improve prognosis of asthma, heart failure, osteoarthritis.and diabetes. However empowering interventions have not been studied in dementia. Therefore, the investigators aim was to examine, in an objective-oriented group intervention, the efficacy of empowerment support program (ESP) on the HRQoL of dementia patients and their spousal caregivers as well as on the sense of competence and psychological well-being of caregivers. Methods: During the years 2014 to 15, 180 dementia patients and their spouses will be recruited from memory clinics or day centers and randomized into two arms: 90 patients for group-based ESP sessions including topics selected by the participants and the use of the by us for us guides, 90 patients will serve as controls in usual community care. Sessions may include topics on dementia, active lifestyle and prevention for cognitive decline, spousal relationship, future planning and emotional well-being. The patients and spouses will have their separate group sessions (ten participants per group) once a week for eight weeks.

NCT ID: NCT02383628 Completed - Quality of Life Clinical Trials

Endoscopic Perfusion Utilizing ICG Fluorescence Technology

ICG
Start date: October 2015
Phase:
Study type: Observational

The main objective of the study is to evaluate the efficacy of indocyanine green (ICG) endoscopy to evaluate tissue perfusion during endoscopic neurosurgery. This includes patients with pituitary and intracranial tumors and treatment of vascular abnormalities such as aneurysms and compressive syndromes. ICG will be evaluated to determine the value of the additional visual information supplied during the treatment of these pathologies.

NCT ID: NCT02374866 Completed - Obesity Clinical Trials

Monitoring Obese Patients : Impact on the Frequency of Monitoring Weight

SUIVIOBESITE
Start date: March 2015
Phase: N/A
Study type: Interventional

The literature data show that long-term monitoring has an effect on weight loss, comorbidity and on improving the quality of life. However, there are still no studies on monitoring obese patients after taking initial multidisciplinary approach. The recommendations of the HAS 2011 advocated "continuous monitoring needed to prevent weight regain, monitor the consequences of overweight and treat comorbidities. This requires a long-term support. "The frequency of follow-up consultations is not specified and "must be adapted to achieve a weight loss target and maintain." Having no specific recommendations on the frequency of monitoring, the investigators chose to experiment closer monitoring than our current monitoring to assess what is the best frequency monitoring, in terms of: weight loss, quality of life, feeding behavior, changes in physical abilities, evolution of comorbidities associated with obesity. The recommendations of the HAS 2011 advocate support of a multidisciplinary obesity for weight loss of 5% to 10 %, which, if maintained, can reduce comorbidities associated with obesity (type 2 diabetes, hypertension, pain associated with osteoarthritis).

NCT ID: NCT02370836 Completed - Quality of Life Clinical Trials

Evaluating the Effects of Psycho-oncological Education on Distress and Quality of Life in Solid Tumor Cancer Patients

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

This study evaluates that effects of psycho-oncological education on distress and quality of life in solid tumor cancer patients who have completed chemotherapy with curative intent. Half of the participants will received a psycho-oncological educational intervention while the other half will receive usual care.

NCT ID: NCT02369055 Completed - Stroke Clinical Trials

Quality of Life and Rehabilitation Pathway in Northern Norway and Denmark.

Start date: March 15, 2014
Phase:
Study type: Observational [Patient Registry]

The aim of this study is to analyze and describe rehabilitation pathways of stroke patients in a region of North Norway and Central Denmark Region in relation to how patients perceive quality of life, health and functioning one year post stroke. The study will consist of 1) Translate, cross-cultural adapt and validate a stroke-specific health-related questionnaire 2) Describe the level of quality of life and rehabilitation pathway in the two countries 3) In-depth interviews of a smaller group of patients for a more complex understanding The study is part of a larger prospective observational multicenter-study of two patient cohorts with stroke.

NCT ID: NCT02367950 Recruiting - Quality of Life Clinical Trials

Exercise as an Intervention in Endometrial Cancer Survivors

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

The purpose of the study is to evaluate the feasibility of introducing an exercise programme for endometrial cancer survivors.

NCT ID: NCT02362750 Completed - Cancer Clinical Trials

Evaluating Cancer Survivorship Care Models

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

The Evaluating Cancer Survivorship Care Models project is an innovative 3-year study that is collecting data to help understand how to best deliver follow-up care to cancer survivors. Cancer is a complex disease requiring complex treatments that can cause lasting impacts after treatment ends. Some patients face physical, psychosocial, spiritual and/or practical challenges as they adjust to life after cancer. Fortunately, health care providers have begun to focus on the consequences of cancer and its treatment and are more actively working with cancer survivors to manage post-treatment needs and care. Led by the George Washington University and funded by the Patient-Centered Outcomes Research Institute, this project brings together representatives from the Commission on Cancer, the Cancer Support Community, LIVESTRONG and the American Cancer Society as well as cancer survivors and healthcare professionals to better understand how different strategies or models of care impact outcomes that are most important to cancer survivors. The project will focus on survivors of breast, prostate and colorectal cancers and will be relevant for understanding the needs and preferences of survivors of other cancers as well. The emphasis is on patient-centered outcomes, which are outcomes that are most significant to patients, such as patient satisfaction and quality of life.