Clinical Trials Logo

Physical Disability clinical trials

View clinical trials related to Physical Disability.

Filter by:

NCT ID: NCT03563820 Completed - Depression Clinical Trials

Resilience and Well-Being Pilot Study

Start date: June 15, 2018
Phase:
Study type: Observational

It is common for Veterans with injuries, illnesses, or physical disabilities to experience depression, post-traumatic stress disorder (PTSD), chronic pain, and other concerns. They may also have goals like becoming happier or better able to cope with challenges that life brings. The purpose of this research study is to learn whether Veterans like and benefit from a 5-week, group-based positive psychology program aimed at improving mental health, resilience, well-being, and quality of life. Participants will be asked to complete several assessments (surveys/interviews) over the course of the study that are not considered part of standard care. Additionally, participants will be asked to participate in a focus group at the end of the study to provide feedback about their experiences in the group.

NCT ID: NCT03545932 Completed - Physical Disability Clinical Trials

Self-perception of Health Status and Physical Condition of Elderly People Practitioners of Hydrogymnastics

Start date: September 1, 2014
Phase: N/A
Study type: Interventional

The researcher interest in self-perception of health status and physical condition of the elderly is determinant in an increasingly aging society and where one should seek to improve their quality of life.

NCT ID: NCT03443375 Completed - Aging Clinical Trials

Exercise Periodization and Older Adults

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

The present study aimed at investigating the effects of two different resistance training protocols — nonperiodized (NP) and daily undulating periodization (DUP) — on hemodynamic, morphofunctional and cognitive parameters of robust older women. Methods: Forty-two older women were randomized allocated into one of the three experimental groups: NP, DUP, and control group (CG). Evaluations of the hemodynamic, morphofunctional and cognitive parameters occurred before, during and after six months. The exercise groups performed the program of exercise twice a week over 22 weeks. In NP, the two weekly sessions were based on 3 sets of 8-10 repetitions at a difficult intensity. However, in DUP, a power exercise session based on 3 sets of 8-10 repetitions at a moderate intensity was added in the first session of the week.

NCT ID: NCT03427294 Completed - Surgery Clinical Trials

Delphi Study on Rehabilitation Following Lumbar Arthrodesis

Start date: January 3, 2018
Phase:
Study type: Observational [Patient Registry]

Delphi study on perioperative rehabilitation after single and double level lumbar arthrodesis.

NCT ID: NCT03411382 Completed - Aging Clinical Trials

Influence of Sit Muscle Strength Training and Game on Elderly

Start date: February 2, 2018
Phase: N/A
Study type: Interventional

Objective: The study aims to understand the physical function, body composition, mental state, behavior, depression, and life quality change of the elderly in a long-term care before and after the intervention. Four interventional activities are sitting strength training, games, sitting strength training with games, and health education.

NCT ID: NCT03392155 Completed - Clinical trials for Spinal Cord Injuries

Performance and Nutrition Program for Athletes in Adaptive Sports

Start date: January 9, 2018
Phase: N/A
Study type: Interventional

Researchers are trying to evaluate and recommend sustainable and effective health and wellness programs for people with spinal cord injury (SCI) and other physical disabilities.

NCT ID: NCT03383601 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Сohort Study to Evaluate Exacerbations, Respiratory Symptoms, Physical Exercise Intolerance and Lung Functions Among Participants Who Use IQOS With Heatsticks Compared to Smokers of Conventional Cigarettes

Start date: December 16, 2017
Phase:
Study type: Observational

This study evaluates frequency of exacerbations, respiratory symptoms, physical exercise intolerance and abnormal lung functions among participants who use IQOS with heatsticks compared to smokers of conventional cigarettes

NCT ID: NCT03305731 Completed - Stroke Clinical Trials

Activating Behavior for Lasting Engagement After Stroke

ABLE
Start date: September 29, 2017
Phase: N/A
Study type: Interventional

Stroke survivors demonstrate high levels of sedentary behavior, placing them at risk for exacerbation of chronic health conditions. This may lead to recurrent stroke. Subtle cognitive impairments are common after stroke and can lead to difficulty self-monitoring and problem solving to overcome barriers to physical activity. Investigators developed the Activating Behavior for Lasting Engagement (ABLE) intervention to promote activity scheduling, self-monitoring, and problem solving activity over the full day. This study examines the effects of the ABLE intervention on sedentary behavior after stroke.

NCT ID: NCT03277027 Completed - Quality of Life Clinical Trials

Health Related Lifestyle and Quality of Life in Children With Cerebral Palsy

Start date: May 26, 2017
Phase: N/A
Study type: Interventional

The primary aim of this study is assessing physical activity, the quality of sleep and health related quality of life in children with cerebral palsy, and parenting stress of caregivers of the children with cerebral palsy in Korea.

NCT ID: NCT03226912 Completed - Depression Clinical Trials

The PREDICT Study- a Registry in Critically Ill Patients to Determine Predictors of Disability Free Survival

PREDICT
Start date: July 18, 2017
Phase:
Study type: Observational

As mortality from critical illness has reduced, the importance of measuring disabilities (cognitive, functional and psychological) in surviving critically ill patients has become more important. Currently, the causes, long-term effects and frequency of disabilities in patients surviving ICU in Australia are unknown. In the US and UK, studies have been undertaken to assess the effects of specific long-term outcomes, such as functional disability and depression, which found long-term disabilities were much higher than baselines (pre-illness function) and ongoing at five years after ICU discharge. In order to improve quality of life of ICU survivors and ensure that medical specialists apply appropriate interventions to reduce the cost of these surviving patients on the community, the PREDICT management committee proposes the introduction of a patient-reported outcomes registry.