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Mobility Limitation clinical trials

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NCT ID: NCT04074252 Withdrawn - Mobility Limitation Clinical Trials

Mobility Impairment in the Northern Region of Malawi

Start date: May 1, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate whether Lofstrand or axillary crutches are better suited to treat mobility impairments and improve physical activity levels in rural, resource-limited, settings like the Northern Region of Malawi. To do this, we are proposing the implementation of a randomized controlled trial (RCT) to measure and compare the physical activity and satisfaction of mobility aid recipients sorted into two groups - one receiving a set of Lofstrand crutches (Group 1) and the other a set of axillary crutches (Group 2). Changes in physical activity, disability, and life satisfaction levels will measured with a follow-up data collection period conducted one year after the distribution of the devices.

NCT ID: NCT04044846 Withdrawn - Frailty Clinical Trials

Promoting Movement in Older Adults in the Community

(ProMO)
Start date: October 7, 2020
Phase: N/A
Study type: Interventional

It is well known that exercise is great medicine, however, for frail older adults who are often homebound and require assistance with personal care, there are gaps in both prescribing this "medicine" and in filling the prescription. The investigators will uncover and address the barriers that prevent frail older adults from increasing their level of physical activity. With input from frail older adults, caregivers, and healthcare providers, the investigators will create a free, easy to use, home-based program that incorporates physical activity such as gentle stretches and range of motion exercises when personal care is being provided. This innovation will add great value to the type of care that is being provided to homebound frail older adults. Incorporating physical activity as part of the care provided offers a unique opportunity for homebound frail older adults to move more, and improve their well-being.

NCT ID: NCT03944473 Withdrawn - Clinical trials for Ambulatory Difficulty

Efficacy and Safety of Sugammadex in High-Risk Ambulatory Surgeries

Sugammadex
Start date: June 20, 2019
Phase: Phase 4
Study type: Interventional

In this randomized controlled study, the investigators hypothesize that sugammadex is superior to neostigmine in higher risk patients undergoing laparoscopic outpatient surgery in an urban, stand-alone ambulatory surgery center. The primary objective of this study is to evaluate the "fit to discharge time in the PACU." The secondary objectives are PACU adverse events, use of additional medications in the PACU, 0-30 day ED or inpatient admissions for a pulmonary diagnosis and patient satisfaction at discharge.

NCT ID: NCT03829163 Withdrawn - Mobility Limitation Clinical Trials

Efficacy and Cost Effectiveness of Utilizing a Hydraulically Adjustable Walker in the Treatment of Hip Fracture

Start date: March 1, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to establish the efficacy of a new walker with hydraulically adjustable legs (HAW) in increasing patients' mobility, especially over uneven terrains such as stairs. An attempt will be made to determine patients' satisfaction with this new instrument as well as comparing it to current walkers' effects on mobility, patient confidence, safety and security. In addition, an estimate of financial advantages/savings will be reviewed. Patient using the HAW should benefit from increased mobility, increased freedom home and in the community, as well as decreased medical costs and need for home modifications along with burden on family members caring for them after the injury.

NCT ID: NCT02298374 Withdrawn - Mobility Limitation Clinical Trials

Evaluation of Homecare Reablement, the Trondheim Model

Start date: November 2014
Phase: N/A
Study type: Interventional

The aim is to evaluate a model of home-based rehabilitation. The intervention targets elder persons who receive homecare services, but still are relatively independent in most activities of daily living. The model focuses on early identification of decline in function and intervention in the home environment through close cooperation between the participant, homecare services and therapists.