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Quality of Life clinical trials

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NCT ID: NCT04632836 Recruiting - Quality of Life Clinical Trials

Consequences of Respiratory Devices on Caregivers (CAP2)

CAP2
Start date: January 20, 2021
Phase:
Study type: Observational [Patient Registry]

The promoter of the study will conduct a monocentric cohort study that aim to evaluate the consequences of home respiratory devices on patient caregivers' quality of life. The investigators will examine the impact of home respiratory devices on quality of life in general, sleep quality, anxiety and humour depending on equipment type (Non-invasive ventilation (NIV), continuous positive airway pressure (CPAP) or long-term oxygen therapy (LTOT)) for patients and partners. The investigators will assess the correlation between patient and caregiver's answers. The investigators will assess the correlation between couple's quality of life and adherence to treatment. To do this, the investigators will use four quality of life questionnaires and the investigators will collect demographic data, medical data and usage report from the equipment.

NCT ID: NCT04632719 Completed - Covid19 Clinical Trials

The MentalPlus® for Assessment and Rehabilitation of Cognitive Function After Remission of the Symptoms of COVID-19

MP-COVID
Start date: November 8, 2020
Phase: N/A
Study type: Interventional

This study evaluates and rehabilitates the cognitive functions of attention, memory, visual perception, language, and executive by the mentalPlus® digital game of COVID-19 surviving patients after remission of symptoms.

NCT ID: NCT04631887 Completed - Quality of Life Clinical Trials

The Delivery of "Doing What Matters in Times of Stress: An Illustrated Guide"

Start date: November 9, 2020
Phase: N/A
Study type: Interventional

The feasibility study for the delivery of the "Doing What Matters in Times of Stress: An Illustrated Guide" will be carried out for Turkish and Syrian individuals with psychological stress. This feasibility study's sample will be adult Turkish and the Syrian refugees. The informed consent form and screening questionnaire of the feasibility study will be sent to the participants who have given this approval and 128 (64 Turkish and 64 Syrian) participants who meet the inclusion criteria will be included in the feasibility study. The psychological problems will be measured twice, before and after the intervention.

NCT ID: NCT04630977 Not yet recruiting - Obesity Clinical Trials

Long-term Intervention Effects of a Personalized, Home-based Exercise Program and Nutritional Advice, Along With the Inclusion of a Pre-workout Multi-ingredient Supplement on the Body Composition, Functional Capacity and Quality of Life of Middle-aged and Older Adults (40-70 Years)

Start date: January 1, 2023
Phase: N/A
Study type: Interventional

The purpose of this study is to analyse the potential benefits of ingesting a commercially available pre-workout multi-ingredient supplement providing ~90 Kcal. for 25g of powder: carbohydrates -isomaltulose, fructose, maltodextrin- 15 g, essential amino-acids -Beta-alanine -L-arginine AKG, L-Leucine, Taurine, L-citrulline- 6.8 g, Creatine monohydrate: 2g, Guarana Extract: 800mg, total caffeine: 160mg, and Magnesium: 112.5mg) vs Placebo CHO intake on body composition, physical performance, Happiness Score (specially designed by our sponsor company, including different self-reported and validated tests on their short form) and every workout: Self-perceived energy feeling and adherence to the intervention.

NCT ID: NCT04629300 Active, not recruiting - Quality of Life Clinical Trials

Supportive Care Mobile Application for Patients With NSCLC

Start date: October 15, 2021
Phase: N/A
Study type: Interventional

This research study is looking at the role of a supportive care mobile app in improving symptoms, coping skills, and quality of life in patients with non-small cell lung cancer.

NCT ID: NCT04628351 Completed - Quality of Life Clinical Trials

Bladder Training in Radical Prostatectomy

Start date: October 10, 2019
Phase: N/A
Study type: Interventional

Radical prostatectomy is the gold standard in the treatment of patients with localized prostate cancer. Urinary incontinence, which is common after surgery, can affect the quality of life of men negatively. There are various attempts to prevent and treat urinary symptoms after radical prostatectomy.The aim of this study is to evaluate the effect of the structured bladder training program on lower urinary tract symptoms and quality of life in patients undergoing radical prostatectomy.

NCT ID: NCT04627935 Not yet recruiting - Quality of Life Clinical Trials

The Effect of Foot Deformities on Physical Activity, Fatigue Level and Quality of Life in Elderly COPD Patients

Start date: March 1, 2021
Phase:
Study type: Observational

The aim of this study is to investigate the effects of changes in foot structure on physical activity level, fatigue and quality of life in COPD patients.

NCT ID: NCT04619264 Completed - Quality of Life Clinical Trials

Impact of Minimally Invasive Restorative Techniques on Pregnant Women Oral Health Related Quality of Life

Start date: January 10, 2019
Phase: Phase 2
Study type: Interventional

Aim of the study was to compare the effect of chemo-mechanical caries removal methods using Papacarie-Duo and alternative restorative treatment (ART) on the Oral Health Related Quality of Life (OHRQoL) of pregnant women.

NCT ID: NCT04614662 Completed - Quality of Life Clinical Trials

Symptom Screening Linked to Care Pathways

Start date: August 2, 2021
Phase: Phase 3
Study type: Interventional

Most children with cancer survive because they are given intensive treatments, but unfortunately, these treatments are associated with distressing symptoms. To address this problem, we developed the Symptom Screening in Pediatrics Tool (SSPedi) so that children receiving cancer treatments can communicate their bothersome symptoms, and Supportive care Prioritization, Assessment and Recommendations for Kids (SPARK), a web-based application that links identified symptoms to supportive care guidelines for symptom management. To establish that these tools improve the lives of children newly diagnosed with cancer, we will conduct a trial that randomizes 20 pediatric cancer institutions and measures the impact of three times weekly symptom screening, symptom feedback to healthcare providers and the development of care pathways for symptom management to improve total symptom burden, fatigue and quality of life.

NCT ID: NCT04611451 Completed - Pain Clinical Trials

Effect of Whole Body Vibration Exercises for Patients wıth Chronic Nonspeific Low Back Pain

Start date: January 1, 2017
Phase: N/A
Study type: Interventional

Whole body vibration (WBV), which is a new treatment method and applied through the device, is defined as mechanical repetitive motion or oscillatory motion occurring around a balance point (5). Chronic nonspecific low back pain is still a serious clinical, social and economic health problem. There are few studies and limited evidence evaluating the effectiveness of WBV exercises in chronic nonspecific low back pain. Different protocols are used for wbv exercise in studies (6). Our aim is to compare the effects of whole body vibration exercise modality on pain, functional recovery, laboor impact, quality of life with control group in patients with chronic nonspecific low back pain.