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Fall Due to Loss of Equilibrium clinical trials

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NCT ID: NCT05902065 Recruiting - Parkinson Disease Clinical Trials

Effect of a Progressive Treadmill Training Protocol for Parkinson's Disease

Start date: July 6, 2022
Phase: N/A
Study type: Interventional

The primary objective of this single-center, no-profit, longitudinal interventional randomized controlled, single-blind trial is to compare the effects of 2 different treadmill training treatments using C-Mill: the experimental one, endowed with augmented virtual reality (AVR) applications, versus the conventional one, the standard treadmill training in PD patients with gait and or balance disturbances. The main questions the study aims to answer are 1) Is the experimental treatment more effective than the conventional one? 2) Is it possible to identify predictive and indicative biomarkers of an outcome measure of rehabilitation using extracellular vesicles (cEVs) assessed by Raman spectroscopy? Participants will be randomized into two groups: the experimental group that will receive the experimental intervention, and the control group that will receive the conventional intervention. Both groups will train three times per week for 8 weeks, the first session starting from 25 minutes (25'). The experimental and the conventional treatments are planned to be progressive and will be individualized to the participant's level of performance. Clinical, neuropsychological, and instrumental variables will be collected at baseline (T0), at the end of the treatment (T1), and 3 months after the end of treatment (T2). At 6 months after the end of treatment (T3), a phone interview will be performed. Both within-group and between-group analyses will be conducted. Biosamples will be collected at baseline (T0) and at the end of treatment (T1).

NCT ID: NCT04752878 Completed - Acute Stroke Clinical Trials

Turkish Version of Ottawa Sitting Scale in Patients With Stroke

Start date: May 15, 2021
Phase:
Study type: Observational

The aim of the study is to describe the cultural adaptation of the Ottawa Sitting Scale and to examine the factor structure, reliability and validity of the scale in patients with stroke. The scale will be translated into Turkish language by following the procedure. 80 patients will be recruited in the study. Berg Balance Scale and Trunk Impairment Scale will be included with Turkish Ottawa Sitting Scale to test the validity. Outcome measures will be repeated by a second physiotherapist the day after the first assessment for interrater reliability and conducted twice within 2 weeks (test-retest) for reliability. The interrater and intrarater reliability of the Ottawa sitting scale will be determined using intraclass correlation coefficients and internal consistency will be assessed using Cronbach's alpha.

NCT ID: NCT03318458 Completed - Clinical trials for Fall Due to Loss of Equilibrium

Pilates Exercises in Spanish Women With Fibromyalgia

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

To analyze the effects of a Pilates exercise program in Spanish postmenopausal women with Fibromyalgia

NCT ID: NCT03201107 Completed - Clinical trials for Fall Due to Loss of Equilibrium

Obesity, Sarcopenic, Risk of Falls in Spanish Postmenopausal Women

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

To analyze the effects of a Pilates exercise program on obesity, sarcopenic, risk of falls and health in Spanish postmenopausal women.

NCT ID: NCT02819011 Completed - Cancer Clinical Trials

OHI--Randomized Control Trial to Evaluate Efficacy, Acceptability, and Perception of Benefit of an Innovative Custom AFO

Start date: May 2016
Phase: Phase 2
Study type: Interventional

The investigators propose a randomized control trial to evaluate long term effects and effectiveness of Moore Balance Brace (MBB) ankle foot orthoses (AFO) in reducing risk of falling in older adults. Primary Endpoints • Characterize the impact of MBB AFO on balance, gait, risk of falling, frailty status, and adverse events Secondary Endpoints • Characterize the Impact of MBB AFO on spontaneous daily physical activities • Characterize the feasibility of the MBB AFO device on patient adherence, acceptability, user-friendliness, and perception of benefit for daily usage