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Quality of Life clinical trials

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NCT ID: NCT01679964 Completed - Quality of Life Clinical Trials

Sustained Virological Suppression and Improvement of Adverse Events of Switching to Raltegravir Study

TaISENWITCH
Start date: July 2012
Phase: Phase 4
Study type: Interventional

Switching from the ritonavir-boosted protease inhibitor component to raltegravir in stable HIV-infected adult patients receiving combination therapy will demonstrate improved clinical tolerability or lipid profiles with sustained plasma virological response (<50 copies/ml).

NCT ID: NCT01669564 Completed - Quality of Life Clinical Trials

Functional Assessment Screening Patient Reported Information

FAST-PRI
Start date: February 2013
Phase: N/A
Study type: Interventional

This study will evaluate a new tool, based on our currently implemented "Functional Assessment Screening Tablets (FAST)," and activate patients to partner with their physicians. Completion of this project, FAST-PRI, will provide important information on the effectiveness of using HIT patient feedback to inform and activate patients and promote health behavior change. Aim 1 Hypotheses: Patients who receive self-management support through HIT patient feedback (intervention) will be more likely than patients who do not receive such feedback (control) to: - Initiate discussions with their provider regarding study-designated PRI; - Have discussions with their providers, regardless of the initiator, regarding study-designated PRI; and - Perceive these discussions of study-designated PRI to be useful. Approach: We will conduct a 12-month randomized controlled trial of HIT patient feedback, clustered at the physician level, in an academic group medical practice. Patients and providers will complete questionnaires regarding discussions of health behaviors and HRQoL at each clinical encounter. Aim 2 Hypotheses: HIT patient feedback will result in: 1) increased number of smoking quit attempts, 2) increased physical activity, and 3) improved mental HRQoL at six, and twelve months. Approach: Patient participants will complete questionnaires regarding smoking quit attempts, physical activity, and their mental HRQoL at baseline, six and twelve months. Aim 3 Hypotheses: For each study-designated PRI, patients who receive HIT patient feedback will: 1) receive more treatment recommendations (e.g., nurse educator, pharmacist, social worker referrals); 2) act on more treatment recommendations; and 3) exhibit improved self-efficacy regarding their ability to make positive lifestyle changes and improve their HRQoL; physicians whose patients receive HIT patient feedback will have higher self-efficacy regarding their ability to influence their patients to make positive lifestyle changes and improve HRQoL. These, in addition to discussions (Aim 1), will mediate the relationship between HIT patient feedback and improvements in study-designated PRI. Approach: We will survey patients and physicians and abstract referral data from the electronic medical record (EMR).

NCT ID: NCT01666470 Completed - Quality of Life Clinical Trials

Quality of Life of Patients With a History of Drug Allergy in Thailand

Start date: August 2012
Phase:
Study type: Observational

Quality of life of patients with a history of drug allergy in Thailand will be studied.

NCT ID: NCT01664585 Completed - Quality of Life Clinical Trials

Exercise Training With Physically Active Lifestyle to Reduce Headache and Quality of Life

HEADEX
Start date: September 17, 2012
Phase: N/A
Study type: Interventional

The aim of this intervention study is to examine whether tailored exercise therapy training is effective and cost-effective to decrease headache frequency and intensity, reduce medication used for chronic headache and patients´ absence from work, improve their neck muscle force, cervical spine mobility, functional ability and quality of life, and increase general physical activity in chronic headache women at regular work during a 6-month intervention. The intervention itself with pilot-tested upper-neck specific exercise regimen aims that patients would independently commit to train and exercise to reduce their headache, and thus increase their quality of life. In addition, reduced pain and frequency of headache may increase the objectively measured daily physical activity of chronic headache patients.

NCT ID: NCT01664013 Recruiting - Quality of Life Clinical Trials

The Impact of Botulinum Toxin Treatment in Quality of Life of Cervical Dystonia Patients

Start date: October 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to investigate the impact of botulinum toxin treatment in quality of life(QoL) in cervical dystonia patients

NCT ID: NCT01663519 Completed - Quality of Life Clinical Trials

Effectiveness of Insoles Provided to Patients With Diabetes. A Longitudinal Randomized Controlled Study in Gothenburg

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

Introduction: Insoles and shoes are frequently prescribed to prevent foot ulcers in patients at risk of diabetes. A combination of neuropathy and foot deformities raises the risk from 1% to between 4-7% according to the Swedish National Board of Health and Welfare, Guidelines Diabetes Care 2010. Preventative care, which includes foot care, annual inspection of the feet, education and prescription of insoles in combination with well fitting shoes are supposed to decrease the risk of ulcers and prevent amputation. Further research is, however, needed to evaluate the effectiveness of these commonly prescribed insoles. The aim of this study is to compare three different types of insoles with respect to pressure distribution. Every 6 months follow-up is assessed until 24 months is reached.

NCT ID: NCT01657487 Recruiting - Quality of Life Clinical Trials

Comparing Treatment Efficacy With High and Medium Dose of Fluticasone in Combination With Salmeterol in COPD Patients

Start date: April 2010
Phase: Phase 4
Study type: Interventional

This study is to investigate and compare treatment efficacy with high and medium dose of fluticasone in combination with salmeterol in COPD patients.

NCT ID: NCT01657175 Completed - Quality of Life Clinical Trials

Quality of Life After Oesophageal or Gastric Cancer Surgery

Start date: January 2009
Phase: N/A
Study type: Interventional

This study aim to assess quality of life of patients 0-5 years after oesophageal or gastric cancer surgery and to develop and test an information and support program aiming to enhance the patients quality of life (QOL) after surgery. The project contains 3 part-studies focusing on the patients life after surgery. Data will be collected through focus group interviews and a randomized controlled trial (RCT) study.

NCT ID: NCT01654900 Not yet recruiting - Quality of Life Clinical Trials

Mid-term Survival and Quality of Life of Elderly Patients Undergoing Open Heart Surgery

Start date: October 2012
Phase: N/A
Study type: Observational

The purposes of the investigators study is to examine the overall survival and quality of life in elderly patients (> 75 years) undergoing open heart surgery at Hadassah medical center between 2008-2011. All alive patients will be phone interviewed using the 36-item short form health survey. Results will be compared to similar health survey results (36-SF)obtained from a group of Israeli adults who had no open heart surgery (controlled group). The investigators hypothesize that elderly patients achieve improvement in quality of life after open heart surgery with acceptable operative morbidity and mortality.

NCT ID: NCT01651078 Completed - Quality of Life Clinical Trials

Laser Ablation After Stereotactic Radiosurgery

LAASR
Start date: July 2012
Phase:
Study type: Observational

The need for new technologies and devices in the field of neurosurgery is well established. In April 2013, FDA cleared NeuroBlate™ System, minimally invasive robotic laser thermotherapy tool. It employs a pulsed surgical laser to deliver targeted energy to abnormal brain tissue caused by tumors and lesions. This post-marketing, multi-center study will include patients with metastatic tumors who failed stereotactic radiosurgery and are already scheduled for NeuroBlate procedure. The study will collect clinical outcome, Quality of Life (QoL) and, where feasible, healthcare utilization data for publication.