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NCT ID: NCT04228900 Not yet recruiting - Malnutrition Clinical Trials

Malnutrition in Older Adults: An Intervention Based on Medication Review and Individual Nutritional Plan

Start date: August 24, 2020
Phase: N/A
Study type: Interventional

The project "Nutrition and Medication management in home-dwelling older adults" consist of two separate studies witch are described in the same study protocol. This is the second study in this Project. The first study (cross sectional) is described separately; Identification: 2017/12883-1 Undernutrition is common in older adults. The causes are many and include drug therapy. Drug side effects, as loss of appetite, nausea, or dry mouth, may contribute to malnutrition, impaired health and loss of function. In patients with malnutrition or at risk for malnutrition we will evaluate an intervention consisting of: - an "individual nutritional plan" with different measures aiming at improving nutritional status. - a systematic drug review.

NCT ID: NCT03338413 Not yet recruiting - Depression Clinical Trials

Cognitive Rehabilitation in Patients With Depression

Start date: January 2018
Phase: N/A
Study type: Interventional

Depression is a highly prevalent and debilitating mental disorder, ranked one of the leading causes of disability worldwide. Several studies have identified neuropsychological deficits in populations of depressed patients affecting domains including attention, memory and executive functioning. These deficits often persist even in patients whose depressive symptoms have remitted. Cognitive impairment in depression represent a core feature of depression, and a valuable target for intervention. Identification of methods that would lead to amelioration would be of great clinical interest, and cognitive rehabilitation (CR) could be a potential way of achieving this. To date few studies on cognitive rehabilitation in depression has been conducted, but the preliminary results are promising. Still the demonstration of long-term effects and evidence relating to improved daily life executive functioning (i.e., generalization) is lacking. In the present study different group-based cognitive rehabilitation interventions will be compared. The aim of the study is to investigate if a group-based "brain training" intervention can improve executive function in patients with active and remitted depression. Efficacy will be assessed immediately after intervention, but also six months after the intervention.

NCT ID: NCT03255356 Not yet recruiting - Anesthesia, General Clinical Trials

Ventilation in Cardiac Surgery

VENICE
Start date: November 1, 2017
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate prospectively ventilatory practices in the perioperative cardiac surgery period.

NCT ID: NCT03191279 Not yet recruiting - Trauma Clinical Trials

First Aid by Laypersons - Effect on Mortality and Length of Stay

Start date: August 2018
Phase: N/A
Study type: Observational

The study aims to assess the effect of first aid from bystanders on survival, admission length, and need of ICU-stay for trauma victims.

NCT ID: NCT02911766 Not yet recruiting - Gingivitis Clinical Trials

Efficacy of Different Chlorhexidine Concentrations

Start date: November 2016
Phase: Phase 4
Study type: Interventional

Chlorhexidine is the gold standard of dental plaque prevention, but which concentration is the most effective is not known. The aim of the present study was to compare the plaque and gingivitis inhibiting effect of commercial products containing 0.2%, 0.12% and 0.06% chlorhexidine in a modified experimental gingivitis model. In three groups of healthy volunteers, experimental gingivitis was induced and monitored over 21days, simultaneously treated with the commercial solutions containing 0.2%, 0.12% and 0.06% chlorhexidine. The maxillary right quadrant of each individual received mouthwash only, whereas the maxillary left quadrant was subject to both rinsing and mechanical oral hygiene. Compliance and side effects were monitored at days 7, 14, and 21. Plaque and gingivitis scores were obtained at baseline and day 21. The commercial mouthwash containing 0.2% chlorhexidine resulted in statistically significantly lower plaque scores than the 0.12 and 0.06% mouthwashes after 21 days use, whereas no statistically significant difference was found between the effect of the two latter mouthrinses. A commercial available mouthwash containing 0.2% chlorhexidine proved statistically significant better effect in preventing dental plaque than 0.12% and 0.06% solutions.

NCT ID: NCT02560259 Not yet recruiting - Referred Pain Clinical Trials

The Role of Referred Pain From the Retro Trochanteric Region in Patients With Knee Pain

Start date: October 2015
Phase: N/A
Study type: Interventional

The role of referred pain from the retro trochanteric region, in patients with knee pain. Defining and quantifying this sub group of knee patients in the investigators list of refered knee patients. Evaluating the effect of treatment. A randomized trial.

NCT ID: NCT02336152 Not yet recruiting - Surgery Clinical Trials

Use of Onepiece Suit or Forced Warm Air for Perioperative Temperature Conservation.

Start date: January 2015
Phase: N/A
Study type: Interventional

To study if a one piece body suite (T-balance, Telespro, Finland) is equally effective in maintaining peri-operative body temperature as forced air warming, during open low-back surgery of medium duration.

NCT ID: NCT01768364 Not yet recruiting - Clinical trials for Ureteric Stent After Stone Surgery

Antibiotic Prophylaxis When Removing Ureteric Stent After Stone Surgery

Start date: January 2013
Phase: N/A
Study type: Interventional

Is there anything to gain in giving antibiotics as prophylaxis when removing ureteric stents cystoscopically after stone surgery?

NCT ID: NCT01681615 Not yet recruiting - Clinical trials for Asthma, Aspirin-Induced

Challenge Test for Acetylsalicylic Acid Hypersensitivity

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

The investigators want to find new challenge test for Acetylsalicylic hypersensitivity / Aspirin hypersensitivity. The investigators suggest that this new test will be as efficient as the already established protocols in terms of sensitivity and specificity.

NCT ID: NCT01624818 Not yet recruiting - Heart Disease Clinical Trials

Active With Heart Disease

Start date: March 2013
Phase: Phase 0
Study type: Interventional

Background: In Norway each year 130-150 children are born with heart disease that requires lifelong medical follow-up. Children with heart defects have reduced motor skills and reduced physical capacity compared with healthy peers. Increased knowledge in the children themselves and the general public, along with psychosocial interventions improve the child's ability to cope with the consequences of their disease. Descriptions of the experiences that Norwegian children with heart disease and their parents have about participation in rehabilitation programs is limited. Geilomo children's hospital has 75 years experience in rehabilitation of children with chronic illness, and started in 2005 to welcome children with heart disease. At present there is no rehabilitation institutions in Norway that has a special group programs for children with heart disease. Geilomo want to establish such a group for children aged 6-7 years and 11-12 years. Main objective: The investigators will use of methods to learn more about the following: Study 1: The purpose is to generate knowledge about how children with heart disease and their relatives experience participation in a rehabilitation program at Geilomo children's hospital. Overarching question: How do children with heart disease and their guardians to participate in a rehabilitation program, and the impact of this on their daily life afterwards? Study 2: The purpose is to help a) to give the children an increased level of activity in the home environment. Question: Will children with heart disease increase their activity levels at home after a stay at Geilomo? 2b) for the children to improve their physical fitness. Question: Will children with heart disease have improved their physical condition three months after a stay at Geilomo? Work schedule: The project will have a duration of 3 years. The project will seek approval of the Regional Committee for Medical Research Ethics in May 2012. Interview Guide, information sheet and consent form has been prepared. Data collection for the study 2AB can start in March 2013. The first interviews will be conducted after 3 months, in June 2013. Data collection is expected to be completed in December 2013. The analysis will take place in parallel with the interview work. In 2014 and 2015 completed the writing of articles (3 pieces) and publication of results. Method: In order to shed light on the problem in study 1, the investigators will use semi-structured interview. 16 children and 16 parents to be interviewed after 3 months. Study 2a) To get information about their child's activity level in the home environment the investigators will use structured questionnaires. It is one form for children (36 persons) and another form for their parents (36 persons). Study 2b) All children (36 persons) conducting physical fitness test at the first visit and after three months. Children can be referred from across the country via the referral form. Dr. Henrik Holm (OUS) and Dr. Asle Hirth (HUS) determines participation according to inclusion and exclusion criteria. Parents submit a written consent on behalf of themselves and their children. Scientific significance: This application describes two related studies, both of which are expected to provide important information that can provide better services for children with heart disease.