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Quality of Life clinical trials

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NCT ID: NCT01132209 Completed - Pain Clinical Trials

Suture Techniques to Reduce the Incidence of The inCisional Hernia

STITCH
Start date: October 2009
Phase: N/A
Study type: Interventional

The objective of the study is reduction of the incidence of the most frequent complication of abdominal surgery, incisional hernia. In this multi center double-blinded prospective randomized controlled trial, in which a new suture technique using small bites is compared with the traditionally applied large bites (mass closure) technique for midline incisions.

NCT ID: NCT01127828 Completed - Quality of Life Clinical Trials

Effects of Cultura Yoghurt in Irritable Bowel Syndrome (IBS) Patients on Intestinal and Immunological Changes

Start date: September 2005
Phase: N/A
Study type: Interventional

To determine the effect of cultura probiotic yoghurt on number of responders to treatment during 8 weeks of treatment in comparison to placebo. To determine the effect of cultura yoghurt on change in total score of (IBS) irritable bowel syndrome severity index during 8 weeks of treatment in comparison to placebo in IBS out patients.

NCT ID: NCT01101711 Completed - Quality of Life Clinical Trials

Endocrine Dysfunction and Quality of Life After Subarachnoid Hemorrhage

Start date: November 2006
Phase: N/A
Study type: Observational

Investigation of the incidence of endocrine dysfunction following subarachnoid hemorrhage (SAH), and to see if this has a relation to CNS lesions as evaluated by MRI and to common symptoms after SAH such as general exhaustion, lack of initiative, increased sleep demand and reduced quality of life.

NCT ID: NCT01080547 Completed - Quality of Life Clinical Trials

Study Comparing Conventional and Fast Track Multi-Discipline Treatment Interventions for Colorectal Cancer

Start date: March 2010
Phase: Phase 3
Study type: Interventional

A new notion"Fast Track Multi-Discipline Treatment" for colorectal cancer is thought with several benefits such as shorter hospitalization stay and less costs. This randomized study aims to compare the differences between conventional and Fast Track Multi-Discipline Treatment for colorectal cancer in hospitalization day, complications, costs and quality of life.

NCT ID: NCT01037946 Completed - Quality of Life Clinical Trials

Family to Family: Psychoeducation to Improve Children's Outcomes in HIV+ Families

Start date: September 2005
Phase: N/A
Study type: Interventional

This project aims to support adults in HIV-affected families in order to improve their well-being. UCLA's Center for Community Health (CCH), in collaboration with the Thai Ministry of Public Health, Bureau of Epidemiology, will implement the Family-to-Family (F2F) intervention in order to improve the social, behavioral and mental health outcomes for families affected by HIV. In Phase 1, the investigators pilot tested the current intervention contents and activities by collecting qualitative data from HIV+ families in the four district hospitals in Chiang Rai and Nakohn Ratchasima provinces selected for the proposed study. The findings from Phase was used to develop intervention content, as well as the format and style of the intervention for Phase 2. In addition, the findings from Phase 1 was used to finalize the assessment measures the investigators will use in Phase 2. In Phase 2, 410 families with HIV+ parents from 4 district hospitals in Chiang Rai & Nakhon Ratchasima Provinces will be recruited to an intervention to benefit their school-aged children aged 6-17 years. At their clinical care site,the investigators randomly assigned families to either: 1) F2F, a psychoeducational intervention for HIV+ parents and family caregivers; or 2) a Standard Care condition. The impact of the F2F intervention will be monitored over 24 months.

NCT ID: NCT01033279 Completed - Quality of Life Clinical Trials

Quality of Life and Efficacy Evaluation of Patient Self-monitoring Their Oral Anticoagulation Therapy

ESCAPE
Start date: October 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether self-management of oral anticoagulation therapy with warfarin has an effect on patient's quality of life following a specific training program led by pharmacists.

NCT ID: NCT01016301 Completed - Quality of Life Clinical Trials

Effects of a Clinical Pharmacist Service on Health-related Quality of Life

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

The aim of the present study is to evaluate effects of a clinical pharmacist service on health-related quality of life and prescribing of drugs.

NCT ID: NCT01006759 Completed - Quality of Life Clinical Trials

Prevention of Disability: Proposal for a Guidance Manual for Leprosy Patients

Start date: January 2007
Phase: Phase 1
Study type: Interventional

Leprosy is an infectious disease of slow evolution, manifested primarily by signs and symptoms dermatoneurological with skin lesions and peripheral nerve, especially in the eyes, hands and feet. The prevention of disability is essential for the control of complications. Objective: To evaluate the physical and functional status of hands, feet and eyes, for the appearance and evolution of sensory and motor deficiencies and classification of disability (WHO) of a group of leprosy patients to compare and monitor the result treatment on the progression of neuropathy and recurrence of reactions. Methodology: We performed initial physical therapy evaluation and final, after 12 months. We conducted a clinical trial of a series of 26 cases evaluated with newly diagnosed leprosy, treated by standard medication. There were used methods of qualitative and quantitative. An illustrated manual of guidelines was especially developed for this study.

NCT ID: NCT01004042 Completed - Depression Clinical Trials

Quality of Life and Self-esteem After Botox® Injections in Depressed and Non-depressed Patients

Start date: October 2009
Phase: Phase 4
Study type: Interventional

The primary objective of this study is to determine the alterations in quality of life and self-esteem after BOTOX® injections in the glabella in depressed and non-depressed patients. The secondary objective of this study are: - to assess wrinkles improvement - to evaluate depressive symptoms using Beck Depression Inventory before and after Botox® injections. - to elucidate that depression is not a contraindication for botulinum toxin injections.

NCT ID: NCT00969020 Completed - Anxiety Clinical Trials

A Telemedicine Solution for Remote Support of Rehabilitation, for Patients Undergoing, Total Hip Arthroplasty Surgery

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

The RRS project is a Randomized Clinical Trial documenting the effect of Remote Rehabilitation and Support via a telemedicine solution for patients undergoing an optimized fast-track orthopedic surgery procedure with the implementation of a total hip arthroplasty. With the telemedicine solution the investigators will support and try to motivate the patient to be discharged after only one day of hospitalization.