Clinical Trials Logo

Life Style Induced Illness clinical trials

View clinical trials related to Life Style Induced Illness.

Filter by:
  • None
  • Page 1

NCT ID: NCT05335382 Recruiting - Clinical trials for Psychological Distress

Implementation and Evaluation of Primary Care Behavioral Health in Sweden

KAIROS
Start date: January 1, 2022
Phase: N/A
Study type: Interventional

In this multicenter study, the investigators want to compare treatment outcomes for patients with mental and behavioral health problems in traditional primary care (Care As Usual, CAU) and primary care centres that work according to the Primary Care Behavioral Health (PCBH) model. In addition to this, the investigators want to study organisation-level outcomes, such as access to care, perceived teamwork and work environment. To achieve this, primary care centres that have expressed interest in implementing PCBH will be cluster randomised between implementing directly or waiting for implementation.

NCT ID: NCT04900064 Recruiting - Depression Clinical Trials

Evaluation of Primary Care Behavioral Health (PCBH) With the Addition of Self-help CBT - A Randomized Multicenter Trial

KAIROS
Start date: June 14, 2021
Phase: N/A
Study type: Interventional

In this multicenter study, the investigators want to find out if an addition of an diagnostic assessment and possibility of treatment with guided self-help CBT can increase the treatment effects of PCBH on patient functioning and symptoms, compared to standard PCBH which uses contextual assessment and brief interventions. In addition to this, the study will investigate the overall effect of PCBH on both patient and organisation level outcomes.

NCT ID: NCT04791085 Recruiting - Covid19 Clinical Trials

Investigation of Stress Levels and Lifestyle of a Sample of Greek General Surgeons in Covid-19

Start date: February 8, 2021
Phase:
Study type: Observational

A new pandemic appeared in early 2020, also known as the coronavirus (Covid-19), affecting all health systems worldwide. Medical and nursing staff make every effort to treat patients resulting in physical and psychological exhaustion, which is exacerbated by the lack of medical and nursing staff, the lack of protective equipment, the increased workload, and increased shifts. In this context, the surgeons had to contribute in turn, in order to help as much as they could in dealing with this new health crisis, as a result of which they find themselves in positions that are not on their subject or in their proper training and to handle patients with a dangerous and highly aggressive respiratory infection. This brought more psychological and physical stress to the surgeons. The pandemic of Covid-19 is not known to be a purely surgical condition, but many patients with coronavirus require surgery due to an additional infection, condition, or complication. The design of this research will be observational and quantitative. Quantitative design involves the provision of numerically coded and analytical measurements, such as self-report questionnaires. The purpose of this cross-sectional research is primarily to record the levels of stress, anxiety, depressive symptoms of Greek surgeons, and their lifestyle. Secondary to correlate the stress levels with socio-demographic data and their lifestyle with other parameters of the study.

NCT ID: NCT04659694 Withdrawn - Frailty Clinical Trials

Effect of an Intervention on Health in Older Care Home Residents

Start date: July 2020
Phase: N/A
Study type: Interventional

Care home residents spent 79% of their time being sedentary. Reduced physical activity and lack of mental stimulation causes general weakness and frailty in older adults that can result in increased healthcare needs. It is important that care home residents spend their time being both physically and psychosocially engaged. This study aims to investigate the effect of a wellness programme on physical and psychosocial wellbeing in older adults living in care homes. Through this process this study will assess the feasibility of implementing the programme and collecting data in care home settings. There are two main groups of participants, 1) care home residents and 2) care home staff. Care home residents will have data collected at three time points. The first time point will be before the intervention (baseline) in the care home setting. The second time point will be three months after the intervention has been delivered. The third time point will be 6 months after the intervention has been delivered. The following measurements will be conducted: 1. Measuring hand grip strength by having to grip a device as firmly as possible and measurements will be taken, 2. Answering questionnaires about quality of life, daily routine, appetite, thoughts about wellness activities the participants have participated in, 3. Wearing a little 'match box-like' device (that measures daily movements and sleep patterns) for 7 consecutive days. Care home staff will be invited to participate in a focus group discussion 6 months after the intervention. Hence, this research will aim to understand the impact of a wellness programme that incorporates physical and psychosocial components that targets the holistic wellbeing of older adults.

NCT ID: NCT03200223 Terminated - Obesity Clinical Trials

Lifestyle Related Disease Management With Wearable Device and Mobile Application

Start date: June 22, 2017
Phase: N/A
Study type: Interventional

In order to study the effectiveness of personalized healthcare intervention for lifestyle-related diseases, investigators designed this study using mobile application and clinical feedback coaching.