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Quality of Life clinical trials

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NCT ID: NCT05747105 Withdrawn - Obesity Clinical Trials

A Sleep Extension Pilot Study in Adults With Obesity

Start date: February 7, 2023
Phase: N/A
Study type: Interventional

The pilot study will test the feasibility of a 16-week sleep extension intervention, in adults with obesity, to increase nighttime sleep duration, as well as reduce daytime sleepiness and sleep-related disturbance. The study will also examine changes in weight, eating behaviors, wellbeing, and blood pressure across the 16-week intervention .

NCT ID: NCT05360745 Withdrawn - Quality of Life Clinical Trials

Quality of Life With Nutritional Supplementation in Patients With Locally Advanced/Metastatic Pancreatic Cancer.

FOODPANC
Start date: June 29, 2022
Phase: N/A
Study type: Interventional

Metastatic pancreatic cancer has a poor prognosis, with approximately one-third of patients experiencing poor quality of life at six months. ARACOMPLEX® is a food supplement that contains maca extract, vitamin complexes and ions, and this nutritional contribution seems to favor the improvement of the patient's quality of life. To verify this statement, this experimental study is carried out in patients with locally advanced/metastatic pancreatic cancer.

NCT ID: NCT05229107 Withdrawn - Anxiety Clinical Trials

Cereset Research For Chronic Nausea

Start date: March 2024
Phase: N/A
Study type: Interventional

This study will explore the use of Cereset Research for symptoms associated with refractory chronic nausea in patients with gastroparesis (GP) in a randomized, clinical trial.

NCT ID: NCT04692389 Withdrawn - Pain Clinical Trials

Jalosome® Soothing Gel Efficacy Grade 2 or 3 Radiodermatitis.

Start date: February 1, 2021
Phase: N/A
Study type: Interventional

Testing the efficacy of the Jalosome® Soothing gel in 2 or 3 grade radiodermatitis healing in oncological patients. The investigators would like to know also the efficacy of the device on quality of life and pain.

NCT ID: NCT04583748 Withdrawn - Depression Clinical Trials

Virtual Health Education vs Meditation in Irreversible Age-Related Vision Loss Patients and Their Caregivers

Start date: April 2022
Phase: N/A
Study type: Interventional

Vision loss is common among older adults and leads to an increased risk for depression and difficulties in daily tasks, thus requiring dependence on caregivers. This study will assess the feasibility of providing two virtual interventions, Sahaj Samadhi Meditation (SSM) and Health Enhancement Program (HEP), to supplement care of patients with irreversible age-related vision loss (IARVL) and their caregivers, with the goal of enhancing mental health and quality of life.

NCT ID: NCT04310488 Withdrawn - Quality of Life Clinical Trials

Assessment of Effects of Museum Prescription of A Montreal Museum of Fine Arts Visit Tour in Primary Care Patients

Start date: July 1, 2022
Phase:
Study type: Observational

The objective of this study is to examine effects on mental and physical health and quality of life in primary care patients visiting the Montreal Museum of Fine Arts (MMFA), this visit being prescribed by their physician. To visit the MMFA and to complete after this visit a series of self-administered questionnaires within the two days after their visit at the museum

NCT ID: NCT04077450 Withdrawn - Quality of Life Clinical Trials

Heart-Focused Breathing in Alzheimer's Disease Caregivers

Start date: January 28, 2019
Phase: N/A
Study type: Interventional

This research study will explore the effects of an online heart-focused breathing intervention on 20 informal caregivers of patients with Alzheimer's Disease (AD) over a period of two weeks.

NCT ID: NCT03627234 Withdrawn - Quality of Life Clinical Trials

Same Day Discharge vs. Overnight Stay After Hysterectomy

SDD
Start date: July 10, 2018
Phase: N/A
Study type: Interventional

In this study patients are randomized between same-day discharge and overnight stay after undergoing a minimally invasive hysterectomy or myomectomy. The goal is to both compare patients' satisfaction and safety and quality of life (QOL) as well as financial consequences between the two groups. The investigators hope to demonstrate that same-day discharge is safe and feasible for most patients with the same level of satisfaction and safety and QOL compared to overnight stay. And also the investigators seek to determine which demographic, medical, social and intra-operative factors influence duration of admission, satisfaction, safety and QOL.

NCT ID: NCT03621397 Withdrawn - Quality of Life Clinical Trials

Online Spanish Cognitive Intervention Program for Spanish-Speaking Latino/Hispanic Subarachnoid Hemorrhage Patients

Start date: December 2021
Phase: N/A
Study type: Interventional

The purpose of this research study is to examine the effectiveness of an online Spanish cognitive intervention program in Latino/Hispanic Spanish-speaking subarachnoid hemorrhage patients. In particular, the researchers will examine whether cognitive impairments associated with a subarachnoid hemorrhagic event improve after completing the online cognitive intervention program. Secondary outcomes of the research study include examining whether there is an improvement in research participants' quality of life and psychological functioning as a result of the online Spanish cognitive intervention program.

NCT ID: NCT03503435 Withdrawn - Quality of Life Clinical Trials

The Effect of Art Therapy on Total Laryngectomy Patients

Start date: July 2019
Phase: N/A
Study type: Interventional

Total laryngectomy (TL) patients suffer from a myriad of psychological and physiological difficulties following surgery. One of their main difficulties in communication due to problems in speaking. Art therapy offers an alternative means of communication via visual art making and has been shown to reduce psychological distress in cancer patients. Thus the goal of our study is to examine the effect of participating in a group art therapy session on the psychological and physical well being of TL patients. Our design is a quasi-experimental qualitative study with a pre-post design, collecting data with validated questionnaires and self-reports of the participants.