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Fractures, Stress clinical trials

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NCT ID: NCT06142305 Completed - DDH Clinical Trials

Supracondylar Femur Fracture After DDH

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

incidence of ipsilateral Supracondylar femoral fractures after cast removal for Developmental dysplasia of the hip (DDH) surgery

NCT ID: NCT06036251 Completed - Stress Clinical Trials

COVID-19 Pandemic Induced Stress and Symptoms

Start date: February 1, 2023
Phase:
Study type: Observational

The previous survey of oncology patients at University of California, San Francisco in 2020-2021 found an alarmingly high symptom burden and high levels of stress and loneliness among respondents. This is a follow-up study with the same sample of oncology patients and survivors who participated in the previous study

NCT ID: NCT05923398 Completed - Distress, Emotional Clinical Trials

Digital Interventions to Understand and Mitigate Stress Response

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

Stress, anxiety, distress, and burnout are exceptionally high among healthcare workers at the frontline of the COVID-19 pandemic. The understanding of factors underlying distress and resilience in complex workplace contexts is limited, and there are limited evidence-based interventions for stress and moral distress among frontline healthcare workers. The purpose of this study is to use a Digital Intervention Suite (a combination of Virtual Reality [VR], a web-based platform, and a wearable [Oura Ring]) to understand and reduce the experience of stress/distress faced by nursing professionals.

NCT ID: NCT05899686 Completed - Stress Reaction Clinical Trials

Effect of Location of Tetanic Stimuli on Photoplethysmogram Under General Anesthesia

Start date: January 27, 2016
Phase: N/A
Study type: Interventional

The effect of the location of tetanic stimulus on photoplethysmography signals will be studied in patients under general anesthesia.

NCT ID: NCT05868798 Completed - Sleep Clinical Trials

Can Ammonium Inhalants Maintain Performance in Sleep Deprived Soldiers?

Start date: October 1, 2020
Phase: Phase 1
Study type: Interventional

This study aims to examine the effectiveness of ammonia inhalants in countering the effects of total sleep deprivation on cognitive and physical performance tests relevant to military personnel.

NCT ID: NCT05786079 Completed - Clinical trials for Tibial Stress Fracture

Effects of Footstrike Transition on Tibial Stress Fracture Risk

Start date: June 1, 2016
Phase: N/A
Study type: Interventional

Biomechanical literature suggests that runners who utilize a mid or forefoot strike pattern may suffer from a reduced incidence of chronic injuries compared to a rearfoot strike. This investigation examined the effects of a 10-week footstrike transition intervention on tibial stress fracture risk in runners.

NCT ID: NCT05512013 Completed - Bone Resorption Clinical Trials

The Effects of NSAIDs on Bone Metabolism Following Exercise

Start date: February 15, 2022
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the effects of a single dose of non-steroidal anti-inflammatory drugs on post-exercise markers of bone and muscle metabolism.

NCT ID: NCT05393206 Completed - Physical Activity Clinical Trials

Influence of Medical Student Coping Behaviour Types on Health Related Behaviour and Stress Level on the Day of OSCE

Start date: May 16, 2022
Phase:
Study type: Observational

Objective structured clinical examinations (OSCEs) have recently been incorporated in the French medical studies. They will soon be an important part of the national evaluation of the students, therefore being responsible for a high level of stress. The differents strategies of coping have never been characterized for this particular group of students. We hypothetize that different strategies of coping are associated with different level of stress, thus being an interesting insight to help students to deal with their stress and prevent disorders linked to stress. We will be using the Brief Cope Scale to assess the different ways of coping, in addition to multiple demographic and health-related questionnaires.

NCT ID: NCT05210205 Completed - Weight Loss Clinical Trials

Physiological Response to Protein and Energy-enhanced Food Products During Winter Military Training

Start date: March 13, 2022
Phase: N/A
Study type: Interventional

Soldiers commonly lose muscle mass during training and combat operations that produce large energy deficits (i.e., calories burned > calories consumed). Developing new combat ration products that increase energy intake (i.e., energy dense foods) or the amount and quality of protein consumed (i.e., essential amino acid [EAA] content) may prevent muscle breakdown and stimulate muscle repair and muscle maintenance during unavoidable energy deficit. The primary objective of this study is to determine the effects of prototype recovery food products that are energy dense or that provide increased amounts of EAAs (anabolic component of dietary protein) on energy balance, whole-body net protein balance, and indices of physiological status during strenuous winter military training.

NCT ID: NCT05172804 Completed - Clinical trials for Stress, Psychological

Mind-Body Modalities for Nursing Students

Start date: October 1, 2020
Phase: N/A
Study type: Interventional

Background: Nursing students around the world can experience tremendous stress due to their multi-faceted responsibilities. Stress is related to negative health and academic outcomes. Mind-body connection modalities have been used successfully to reduce stress and improve health among healthy and ill individuals in various cultures, but their effects have not yet been studied in the Arab culture. Thus, the purpose of this study was to examine and compare the effects of three of such modalities including progressive muscle relaxation (PMR), guided imagery (GI), and mindfulness meditation (MM) on stress and health outcomes in Jordanian nursing students. Methods: Using a randomized controlled design, 124 nursing students will be randomly assigned to 4 groups at a large university in Jordan. The 3 experimental groups (PMR, GI, and MM) will participate in 5 30-minute sessions (one session/week for 5 weeks) led by experienced trainers, in a private room during their clinical days. The control group will stay calm for 30 minutes during introducing the study interventions in another room at the university. The health outcomes will be measured at baseline (Time 1) and the end (Time 3) of the intervention in each group using different physical and self-report measures classified into different health categories such as cognitive health outcomes (executive brain function, stressful appraisal, mindfulness), physical health outcomes (e.g. physical symptoms, heart rate, blood pressure, neurobiological markers such as dopamine, serotonin, cortisol, adrenaline, and noradrenaline), and psychological health outcomes (e.g. depression, anxiety).