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Quality of Life clinical trials

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NCT ID: NCT01254253 Unknown status - Quality of Life Clinical Trials

Functional and Clinical Benefits of PCI in Patients With CTO

Start date: October 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the diagnostic accuracy of hybrid imaging combining CTCA with low-dose stress-only SPECT vs. coronary angiography for detecting haemodynamic relevant coronary lesions; and second to determine the effects of PCI on cardiac perfusion, cardiac function and quality of life in patients with CTO lesion in left anterior descending (LAD) coronary artery.

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: NCT01228864 Terminated - Quality of Life Clinical Trials

Brody Belt - Alternative Method of Securing a Patient's Urinary Drainage Bag

Start date: September 22, 2009
Phase: N/A
Study type: Interventional

The Brody belt may help improve quality of life in patients using urinary drainage bags. PURPOSE: This clinical trial studies the Brody belt in improving the quality of life in patients using urinary drainage bags.

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: NCT01202812 Not yet recruiting - Quality of Life Clinical Trials

A Randomized Trial of LOVAZA in Pediatric Sickle Cell Disease (SCD)

Start date: October 2010
Phase: Phase 2
Study type: Interventional

The purpose of the study is to determine the effectiveness of LOVAZA (fish oil capsules) to decrease inflammation in children and adolescents with Sickle Cell Disease (SCD). It has been found that besides the damage caused by sickle red blood cells themselves, the inflammatory response that occurs in SCD patients could potentially play a significant role in the occurrence of painful episodes or pain crises. The investigators will also study whether the subject/caregiver feels that there is an improvement in the child's quality of life by taking the medication. Besides the effect of LOVAZA on inflammation,the investigators are also testing whether the drug will have a beneficial effect on blood clotting ability (which is known to be increased in SCD) and on the anemia (low red blood cells) that is part of the disease entity.

NCT ID: NCT01192594 Terminated - Schizophrenia Clinical Trials

Milestones of Adjustment Post-Psychosis

MAPP
Start date: November 2009
Phase: Phase 3
Study type: Interventional

This nested design clinical outcome study of psychiatric case manager education on disease state, psychopharmacology of schizophrenia, relapse, motivational interviewing, and the process of psychological adjustment post-psychosis (Milestones of Adjustment Post-Psychosis Recovery Model-MAPP) will test the following hypotheses: 1. Medication non-adherence in patients with schizophrenia assigned to case managers who receive MAPP training will decrease from their pre-study rate and from the reported national average after one year enrollment compared to consumers not enrolled in the MAPP arm of the study. 2. Consumers in the MAPP intervention will have higher Quality of Life Enjoyment and Satisfaction Questionnaire (Q-Les-Q (53) scores than consumers not enrolled in the MAPP at quarterly measures. 3. Consumers enrolled in the MAPP intervention arm of the study will successfully complete the first two phases of the MAPP Recovery Model in one year. 4. Consumers in the MAPP intervention arm will have greater symptom reductions at quarterly data points compared to consumers not enrolled in the MAPP intervention arm.

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.