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Quality of Life clinical trials

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NCT ID: NCT01241890 Completed - Quality of Life Clinical Trials

Prevention of CF Exacerbation in Childhood: PREVEC Study

PREVEC
Start date: October 2011
Phase: N/A
Study type: Observational

Pulmonary exacerbations of CF are an important cause for the experienced disability of patients, respiratory symptoms, and decreases in lungfunction, which require antibiotic therapy at home or in the hospital. Therefore, prevention of exacerbations in CF is important. The aim of this study was to assess the predictive properties of inflammatory markers in exhaled breath for pulmonary exacerbations in children with CF. In addition the reliability of home monitor assessments of symptoms and lungfunction was investigated.

NCT ID: NCT01231256 Completed - Quality of Life Clinical Trials

Preventive Health Consultations With Young Adults With Multiple Problems

Start date: February 1998
Phase: N/A
Study type: Interventional

A new working method, i.e. a questionnaire completed at home followed by a patient-centred preventive health consultation with follow-up, can be used by all general practitioners (GPs) as a preventive offer to their patients with multiple problems in lifestyle, well-being or health behaviour, if this project is shown to be effective. The investigators use a broad preventive offer in a structured way to young adults with multiple psychosocial problems (a certain risk profile) found by a screening questionnaire when arriving to the clinic. The main hypothesis of the project is: By using the questionnaire and subsequent patient-centred health consultation the GP is able to support the participants to improve their resources, their well-being and self-estimated health. Subsequently, relevant changes in health habits and life situation might be initiated in order to prevent or reduce future problems or illness.

NCT ID: NCT01204567 Completed - Quality of Life Clinical Trials

The Influence of Exercise on Mental Health After Discharge From Hospital

Start date: January 2010
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the effect of aerobic fitness training on mental health (health-related quality of life),cognitive and physical capacity in older people discharge from hospital and to assess if further aerobic training at home enhances the effect. Design: Randomized controlled trial conducted at Oslo University Hospital, department of Medicine in conjunction with Oslo University College. The subjects will be randomized into one intervention group (training group) or one control group. Outcome measure: Health-related quality of life Physical function Cognitive capacity Physical activity Body composition Physical activity level

NCT ID: NCT01184547 Completed - Quality of Life Clinical Trials

Effects of a Community Based Exercise Program in Adults With Severe Burns

COMBEX
Start date: April 2010
Phase: N/A
Study type: Interventional

The purpose of this proposal is to assess the efficacy of implementing a 12-week structured and supervised community-based exercise program (COMBEX) at hospital discharge. The investigators will assess the effect of exercise on mental health and physical function, along with its effects on the amelioration of the burn-induced catabolic response. The central hypothesis of this proposal is that exercise-induced physical and psychosocial benefits obtained during a supervised and structured COMBEX program in severely burned adults will improve physical function, and quality of life relative to Standard of Care (SOC).

NCT ID: NCT01177930 Completed - Quality of Life Clinical Trials

Evaluation of the Health Related Quality of Life and Disease Prevalence of Children From Spain at 6-8 Years of Age Who Participated in a Qualifying Infant Formula Study at Birth

Start date: October 2009
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate the influence of the type of feeding in the first year of life on the behavior and health-related quality of life at 6-8 years of age.

NCT ID: NCT01174524 Completed - Quality of Life Clinical Trials

Improvement of Quality of Life in Patients Using Low-dose Pills in the Different Phases of Menacme

Start date: January 2008
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether low-dose contraceptive pills are effective in the improvement of quality of life in patients in the different phases of menacme.

NCT ID: NCT01173861 Completed - Breast Cancer Clinical Trials

Effectiveness of a Cancer Center Based Physical Activity Intervention

Start date: March 2010
Phase: N/A
Study type: Interventional

Purpose: Examine the effectiveness of cancer center-based physical activity counseling on physical activity rates and quality of life in breast cancer survivors. Hypothesis: Participants in the intervention group will indicate greater step counts and quality of life at the end of the intervention compared to the control group

NCT ID: NCT01167855 Completed - Asthma Clinical Trials

Reducing Asthma Disparities Through School-Based Telemedicine for Rural Children

Start date: May 25, 2011
Phase: N/A
Study type: Interventional

The overall goal of this proposal is to examine the efficacy of a school-based asthma telemedicine intervention in a predominately minority, low-income rural pediatric population.

NCT ID: NCT01155011 Completed - Quality of Life Clinical Trials

Multilevel Intervention for Physical Activity in Retirement Communities

MIPARC
Start date: January 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to assess whether a 6-month multilevel physical activity intervention can significantly increase physical activity levels in sedentary adults, 65 and older, living in Continuing Care Retirement Communities (CCRCs). Sedentary residents (N=320)in 16 CCRCs will receive the multilevel MIPARC intervention or a control health education program for 6 months. A group randomized control design will be employed with site as the unit of randomization. The intervention is delivered through group sessions, phone calls, printed materials, tailored signage and mapping and targeted peer led advocacy efforts.

NCT ID: NCT01140659 Completed - Quality of Life Clinical Trials

Objective Evaluation of Patients With Palmar Hyperhidrosis Submitted to Two Levels of Sympathectomy: T3 and T4.

Start date: February 2007
Phase: N/A
Study type: Interventional

Compare the results obtained with video-assisted sympathectomy performed in two distinct levels ganglionic (third versus fourth thoracic ganglion) for the treatment of palmar hyperhidrosis, through a blind randomized clinical trial using an objective method to measure the sweat before and after the operation.