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Mobility clinical trials

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NCT ID: NCT06400134 Completed - Frailty Clinical Trials

Coginitve and Physical Functions in Geriatric İndividuals

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

The aim of this study is to investigate the relationship between cognitive functions with physical performance, grip strength, walking speed, mobility, and frailty in geriatric individuals. Decline in cognitive function and decline in physical performance are generally associated with advanced age. Cognitive dysfunction is a natural consequence of ageing and is an important factor in maintaining quality of life and independence. Investigating the relationship between cognition, physical performance, mobility, and frailty has become a challenging issue in recent years. However, there is a need to further clarify the direction of this cognitive-motor link.

NCT ID: NCT06269224 Completed - Range of Motion Clinical Trials

Examining Factors Influencing Thoracolumbar Mobility in Runners

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

The presence of to is thoracolumbar (TL) mobility a significant aspect in the context of running. Most of the factors may be related to certain kinematic parameters of the lumbopelvic-hip complex during running.

NCT ID: NCT05878756 Completed - Clinical trials for Hemiplegic Cerebral Palsy

Effects of Additional Functional Strength Training on Mobility in Children With Hemiplegic Cerebral Palsy

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

The randomized control trail was to determine the effects of additional functional Strength Training on mobility in Children with Hemiplegic Cerebral Palsy.

NCT ID: NCT05679947 Completed - Pain Clinical Trials

Mobilization Protocol for Knee Arthroplasty Patients

KA-Mobility
Start date: May 1, 2022
Phase: N/A
Study type: Interventional

This randomized controlled study evaluates the effect of mobilization protocol applied to knee arthroplasty patients on anxiety level, pain, mobility and functional status.

NCT ID: NCT05196997 Completed - Critical Care Clinical Trials

The De-Morton Mobility Index Turkish Version in Intensive Care Patients

Start date: April 1, 2018
Phase:
Study type: Observational [Patient Registry]

De Morton Mobility Index is recommended for the evaluation of mobility in the evidence-based guidelines, in patients in intensive care units. The aim of our study is to examine the validity and reliability of the Turkish version of the De Morton Mobility Index in patients hospitalized in the respiratory intensive care unit.

NCT ID: NCT04858685 Completed - Mobility Clinical Trials

Early Mobilization After Arthroplasty

Start date: November 7, 2017
Phase:
Study type: Observational [Patient Registry]

Aims and Objectives: This study was conducted in order to determine the factors that affected the early mobilization after surgery of patients who had undergone knee and hip arthroplasty. Background: Early mobilization in knee and hip arthroplasty is still not at the desired level, and it is among the most frequently overlooked nursing practices. Desing: This study is descriptive and cross-sectional. STROBE checlist was used to compile the study's report. Methods: The universe of the study consisted of a total of 80 patients who were hospitalized between 07 November 2017 and 21 September 2018 in the Orthopedics and Traumatology Clinic of a State Hospital to undergo knee or hip arthroplasty, and who met the inclusion criteria. The sample of the study consisted of 60 patients who were in the universe of the study, who met the inclusion criteria and who voluntarily agreed to participate in the study.

NCT ID: NCT04420910 Completed - Parkinson Disease Clinical Trials

Non-motor Symptoms, Balance, Muscle Strength, and Functional Mobility in Patients With Parkinson's Disease

Start date: April 15, 2019
Phase:
Study type: Observational

The purposes of this study is to examine balance, muscle strength, and mobility in relation with non-motor symptoms (NMSs) in patients with Parkinsosn's Disease (PD). NMSs have been shown to be the key determinant of health-related quality of life (HRQoL) and have a greater effect on HRQoL compared to motor symptoms.Despite a growing literature on NMSs, there are few data on the association between NMSs and motor phenotypes of PD, and they have usually focused only on specific domains of NMSs, such as cognition, mood/anxiety issues, or sleep disorders. When literature is examined, there is no study which examines balance, muscle strength, and mobility in relation with NMSs in patients with PD.For all these reasons, we think that balance, muscle strength, mobility, and NMSs in patients with PD are worse than those of the healthy individuals and that there is a relationship between NMSs and motor symptoms.

NCT ID: NCT03988751 Completed - Surgery Clinical Trials

Real-time Location System Feasibility Study

Start date: June 6, 2019
Phase: N/A
Study type: Interventional

The proposed study will investigate the feasibility of using the Wake Forest Real-time Location System (RTLS) in monitoring patient movement during their in-hospital postoperative recovery. The study will involve patients who have undergone surgery requiring inpatient admission to the surgical ward. Actual patient movement will be monitored during their postoperative recovery and compared with data recorded by the Wake Forest location system. In this small pilot study, a subgroup of participants will be randomized to two cohorts, continuous walking and interval walking. Tolerability of the varied walking intensity will be measured.

NCT ID: NCT03578861 Completed - Dementia Clinical Trials

Dementia Specific Respite Care Concept.

DESKK
Start date: October 20, 2017
Phase: N/A
Study type: Interventional

Objectives: Specific mobility programs can delay the functional decline in people with dementia (PwD) and help to preserve their abilities of daily living. Respite care is a common used short time inpatient service (max. 4 weeks of stay) to support dementia care arrangements. Within the DESKK project, a concept is developed which complements and optimizes dementia-specific respite care through a mobility program and a counseling program. As one part of the DESKK study, it is the aim to develop and implement a time effective and evidence based mobility program for PwD in respite care which can be individually adapted on PwD needs and preferences. It includes a short "homework-program" for caring relatives to facilitate ongoing mobility training of the PwD after returned back home. Methods: A pilot based, quasi-experimental evaluation study is conducted in a specialized respite care facility for PwD. The concept was developed on the basis of a comprehensive literature research, study visits at existing counseling programs as well as expert workshops with practitioners and scientists. To evaluate the implementation process, qualitative data are collected by single und group interviews. Quantitative data are collected using validated instruments to assess mobility and cognitive function of PwD. A mixed methods triangulation approach will be used to aggregate qualitative and quantitative data. Discussion: It is expected that the RC concept will be suitable and understandable for the staff, so that it can be implemented in the RC facility. As a result of the mobility program, the physical abilities of the PwDs should improve. Similar, the burden of the caregivers should be reduced by combined effects of the counselling program and the higher mobility level of the PwD. The whole DESKK concept, including a systematic counseling program for caring relatives, which is not part of this presentation, will be described in form of a practice friendly website to get disseminated into clinical routine after its successful evaluation.

NCT ID: NCT02833779 Completed - Mobility Clinical Trials

Trial to Compare the Effectiveness of Group Versus Individual Therapy on Alternate Days in Patients With Subacromial Impingement Syndrome

Start date: April 2010
Phase: N/A
Study type: Interventional

Pathology of the rotator cuff and subacromial bursa is considered to be the principal cause of pain and symptoms arising from the shoulder. Physiotherapy specialists often disagree about which type of exercise is most appropriate. Manual Physiotherapy combined with guided exercise is a commonly applied clinical treatment, but no proof of its effectiveness has been shown. Clinical trials comparing results of treating subacromial syndrome of the shoulder with guided self-treatment and conventional physiotherapy yielded a slightly higher improvement, basically because patients suffered from chronic tendinitis and the treatment period lasted only two weeks. That is the reason why the investigators propose a long-term follow-up study and a more complete assessment of effectiveness of the exercise prescribed to improved this pathology. Objectives: - Assessment of effectiveness of two different types of treatment of subacromial syndrome of the shoulder. - Comparison of effectiveness of both treatments in order to select that one yielding better results as the one to be applied as a routine practice. Patients will be assigned one of the following treatments: - Group 1: patients will be taught exercises in groups of six people, on a daily basis for twelve sessions. - Group 2: patients will be taught the same exercise as Group 1, individually, and will receive manual therapy consisting of muscular and joint re-centering. A modified version of the Constant scale will be used to assess mobility and pain shoulder.