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Quality of Life clinical trials

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NCT ID: NCT03766945 Recruiting - Quality of Life Clinical Trials

Fatigue and QoL Among Gastric Cancer Patients Undergoing Abdominal Surgery

Start date: July 27, 2017
Phase:
Study type: Observational [Patient Registry]

Background: Cancer-related fatigue (CRF), one of the indicators of QoL, is one of the most common side effects of cancer and its treatment. However, the pathophysiological mechanisms involved in CRF among cancer patients are not completely understood. Therefore, more in-depth researches on CRF of surgical patients suffering from gastric cancer are needed in Taiwan. Purpose: The purpose of this study is to examine the incidence rate and correlated factors (QoL and immune biomarkers) of CRF among gastric cancer patients undergoing major abdominal surgery. Method: A longitudinal study was conducted to recruit gastric cancer patients who scheduled to operate at surgical clinics from a northern medical center in Taiwan. The data will be collected with a structured questionnaire and Immune markers assessments via purposive sampling of 120 subjects. Before operation, on day 1 after operation, and on day 7 after operation, the biomarkers will be measured. The BFI-T questionnaire will be filled out before surgery and on day 1, 2, 7, 28 after surgery; The EORTC QLQ-C30 and EORTC QLQ-STO22 questionnaire will be filled out before surgery and on day 7, 28 after surgery; Type D scale-14(Taiwanese version) questionnaire will be filled out before surgery and on day 28 after surgery. Data will be analyzed by using descriptive statistics, paired t-test, Chi square test, Pearson's correlation, and the generalized estimating equation (GEE) was used to identify significant factors with QoL after operation. Anticipated achievement: The anticipated achievement of this study is to provide healthcare providers with more knowledge about CRF, and help them to enhance the quality of life on gastric cancer patients in the future.

NCT ID: NCT03766360 Not yet recruiting - Depression Clinical Trials

Bariatric Surgery Study

SIBS
Start date: January 2019
Phase: N/A
Study type: Interventional

The current study proposes an open clinical trial to investigate the effectiveness of a social functioning intervention on bariatric surgery outcomes and depression. The treatment will be administered in a group format over 10 weekly/biweekly sessions and will take place at the University of Washington Weight Loss Management Clinic (WLMC) at the Roosevelt Clinic location. Effects of the intervention will be measured with self-report questionnaires and by self-report of behaviors outside of assessment sessions (via questionnaires and self-report of adherence to treatment). Data collection will occur at specific time points including before treatment, after treatment, and two months after treatment.

NCT ID: NCT03763500 Recruiting - Atrial Fibrillation Clinical Trials

Evaluation of the Added Value of an Internet-based Educational Program for Patients With Atrial Fibrillation.

AMADEUS
Start date: December 3, 2018
Phase: N/A
Study type: Interventional

This study is prospective, open and randomized concerning the value of an Internet-based educational program for patients with atrial fibrillation compared to "care as usual".

NCT ID: NCT03762941 Completed - Quality of Life Clinical Trials

Quality of Life Among Acute Admitted Elderly

Start date: August 1, 2018
Phase:
Study type: Observational

Elderly dependent on homecare, admitted acutely, are fragile. The aim of this study is to investigate the difference in the definition and rating of Quality of Life (QoL) among acute admitted elderly i) with and ii) without homecare background.

NCT ID: NCT03761199 Completed - Quality of Life Clinical Trials

Assessment of the Impact of Whole Body Cryostimulation on Skin Physiological Indicators

Start date: November 26, 2018
Phase: N/A
Study type: Interventional

The aim of the planned study will be to evaluate the effect of repeated cryostimulation treatments on immunological, morphological, and biochemical indicators of the peripheral blood of patients with atopic dermatitis (AD). The aim of the study will be also to measure the oiling, hydration and pH of the skin of patients with AD after a series of treatments in a cryogenic chamber. Each participant will complete a Brief Questionnaire on Quality of Life, Life Satisfaction Index, Self Evaluation Questionnare and DERMATOLOGY LIFE QUALITY INDEX (before and after the WBC procedures).

NCT ID: NCT03756441 Recruiting - Quality of Life Clinical Trials

Effects of the MBHP on the Quality of Life of Family Members of People With Intellectual Disability

caregivers
Start date: February 1, 2019
Phase: N/A
Study type: Interventional

The research aims to verify the effects of the Mindfulness Based Health Promotion (PSBM) program on the quality of life of mothers of person with intellectual disability. Method: A randomized, controlled study with pre-post intervention measures and a follow-up measurement will be performed after six months of the end of the intervention. Sample: It will be composed of mothers of the 209 attended with moderate intellectual disability, adolescents and adults of the Service of Socioeducation of the Association of Parents and Friends of the Exceptional (APAE) of São Paulo, excluding those who have any psychiatric problem in the acute phase and minors, or who have regular practice of mindfulness or meditation in the last 6 months.

NCT ID: NCT03753932 Completed - Quality of Life Clinical Trials

Impact of Fixed Dentures in Head and Neck Cancer (IMFDHAC)

IMFDHAC
Start date: March 1, 2013
Phase: N/A
Study type: Interventional

The purpose of the multi centre study is to evaluate an intervention, which means that patients undergoing radiotherapy for head and neck cancer will receive fixed dentures in accordance with the Public Health Care fee system with regard to well-being and oral health related quality of life. Hypotheses: the intervention will improve oral health related quality of life, general wellbeing, and nutrition in patients treated by radiotherapy, with or without combination of chemotherapy or surgery against head and neck cancer.

NCT ID: NCT03753035 Recruiting - Quality of Life Clinical Trials

Observance of Anticonvulsant Treatments and Quality of Life of Epileptic Children

ObEPI
Start date: November 29, 2018
Phase:
Study type: Observational

There is little epidemiological data in the literature on the therapeutic compliance of epileptic children. Yet it is a fundamental issue in the therapeutic education and balance of this pathology. To obtain more epidemiological precision on the observance of epileptic children and to propose, according to the factors involved, the improvement of practices (therapeutic education ..). Propose an evaluation of the quality of life of their children by a suitable self-questionnaire.

NCT ID: NCT03751319 Completed - Quality of Life Clinical Trials

Geriatric Assessment and Intervention for Older Patients With Frailty in the Emergency Department

GAOPS
Start date: December 11, 2018
Phase: N/A
Study type: Interventional

Comprehensive Geriatric Assessment (CGA) is an established approach for better detection of frailty-related problems and includes individualized treatment plan with multi-discipline supportive and treating measures for the older frailty patients. However, there is limited evidence of feasibility and efficacy of the CGA when provided in the emergency department setting. In the GAOPS-study the efficacy of the CGA in emergency department setting will be studied by randomized controlled study protocol. We aim to study if the CGA provided in the ED is feasible, safe and efficient method when added with standard emergency care for older frail patients.

NCT ID: NCT03745599 Completed - Pain Clinical Trials

Evaluation of the Effects of Different Analgesics on Pericoronitis Pain and Quality of Life

Start date: November 1, 2017
Phase: Phase 4
Study type: Interventional

Pericoronitis is a painful inflammatory condition which is well known for its negative impact on quality of life of those affected. The aim of this study was to test two hypotheses: (1) that topical application of Benzydamine is as effective as oral Diclofenac or Flurbiprofen in improving pain and quality of life of patients with pericoronitis and (2) that there would be no difference between the effects of the two oral NSAIDs on pain and quality of life of patients with pericoronitis