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Activity clinical trials

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NCT ID: NCT06407557 Completed - Activity Clinical Trials

Optimizing Older Adults' Home Space for Physical Activity

Start date: January 1, 2024
Phase: N/A
Study type: Interventional

There will be a multi-channel approach to recruitment. Currently, ongoing projects within diverse communities lead in Swansea, Bridgend, and Neath Port Talbot will be approached, and this research will recruit alongside these projects. Regional coordinators and sub-coordinators will be contacted for recruitment, to best ensure participating older adults reflect the typical socio-demographics of Wales. This network will help the researchers to reach older adults who previously took part in different projects. Recruitment letter posters/leaflets will be used as an enrolment technique. Furthermore, the researchers will place advertisements across the University using the intranet and work alongside the City and County of Swansea, Neath Port Talbot, and Bridgend Borough Council to recruit using their sport, play, and community networks. The first stage of recruitment involves approaching diverse community organizations to formally request approval to recruit via their contacts. In-stage gatekeepers will be approached by the researcher to seek permission to contact potential participants via their organization. All interested participants will be asked to contact the researcher directly to further discuss the study and indicate their interest. All participants will provide written informed consent to participate in the study before the baseline assessment is conducted. Moreover, each older adult will receive a sleeping log (to record not wearing time), an accelerometer device, and instructions on how to attach and wear the device for 7 consecutive days. The primary researcher will be contacted if older adults have any queries or issues with the device. The participants will be subsequently randomized to an intervention group or comparison group on the basis of 1:1 allocation. All assessments including questionnaires and a 7-day accelerometer assessment will be repeated post-intervention. An Independent t-test will be run to assess the pre-post difference in the effectiveness of the trial in the intervention and comparison groups. The regression model will be applied to assess the impact of covariates with the dependent variables (MVPA, daily step count, self-efficacy, well-being, and sedentary behaviour). Qualitative data analysis of interview data will use reflexive thematic analysis to illustrate common themes regarding the acceptability of the feasibility trial.

NCT ID: NCT05152251 Recruiting - Quality of Life Clinical Trials

Activities and Participation of Children With Down Syndrome

Start date: February 1, 2021
Phase:
Study type: Observational

The aim of this study is to examine the activity participation levels of Down syndrome(DS) children and the restrictive or supportive factors affecting their participation levels and to investigate their effects on quality of life. 35 children diagnosed with DS by a pediatric neurologist and 35 typically developing children are planned to be included in this study. Sociodemographic data of typically developing and DS children who agreed to participate in the study and their families will be questioned. Activity (Gross Motor Function Measurement-GMFM-88) , participation and the effect of the environment on participation (Participation and Environment Measure for Children and Youth-PEM-CY ), reflection of motor development levels to functions in daily living activities (Pediatric Evaluation of Disability Inventory- PEDI) , quality of life(Pediatric Quality of Life Inventory- PedsQL) and familial impact (Impact on Family Scale-IPFAM) will be evaluated. Evaluation methods to be used in our study will be applied one-on-one with children and face-to-face interviews with their parents. Our study is important in that there is little evidence on participation studies in children and that changing medical paradigms emphasize the quality of life of children. In addition, the PEM-CY the investigators will use in the study will make the study more valuable as it examines the effect of the environment on participation and evaluates participation in different environments.

NCT ID: NCT03825497 Terminated - Hospitalization Clinical Trials

The WALK-Copenhagen Trial (WALK-Cph): a Mixed Methods Study

Start date: September 25, 2018
Phase: N/A
Study type: Interventional

The WALK-Copenhagen project aims at enhancing physical activity during and after hospitalization in older medical patients by an intervention developed in co-operation with key stakeholders

NCT ID: NCT03640611 Completed - Cerebral Palsy Clinical Trials

Investigating the Relation Between Environmental Factors and Activity-participation in Children With Cerebral Palsy

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

Cerebral palsy (CP) is a chronic condition that causes the most childhood disabilities on worldwide. Impairment in movement and posture development seen in children with CP it causes difficulties in performing activities and affect in emotional, social, and cognitive abilities cause limited participation in everyday life. The ICF-CY child is divided into five categories: body structure and functions, activities, participation, environmental and personal factors, it is treated holistically. Initially, children with CP have adopted the view that environmental factors can also affect functionality, while focusing on the treatment of motor disorders to reduce activity and participation limitations in physiotherapy and rehabilitation applications. Environmental factors; the environment in which the child lives, his family, the devices he uses, health and care services, and government policies. These factors vary according to each country's own cultural and economic opportunities. The investigator planned to do this study because we found that there is a need for a comprehensive study of children with SP in Turkey, which does not reveal the relationship between environmental factors and activity and level of participation.

NCT ID: NCT02840838 Not yet recruiting - Pain Clinical Trials

Botulinum Toxin for Post Abdominoplasty Pain Control

Start date: December 2018
Phase: Phase 4
Study type: Interventional

We are investigating ways to reduce pain after abdominoplasty. We hypothesize that injection of Dysport (botulinum toxin A) into the rectus abdominis, abdominal wall musculature, during abdominoplasty will provide a more effective, longer lasting method for pain control than standard of care alone (use of Exparel (liposomal bupivacaine) intraoperatively followed by PRN narcotics. We will randomize patients to receive either Disport + standard of care or saline (placebo) + standard of care and compare post operative pain for the following 2-3 months.

NCT ID: NCT02786394 Completed - Aging Clinical Trials

Return to Everyday Activities in the Community and Home

REACH
Start date: May 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to test feasibility for the delivery and perceptions of a lifestyle model for middle-aged and older adults by involving participants in its development. The goal of the program is to reduce sedentary behaviour, increase physical activity, and increase strength and balance. An optional walking program will be run in parallel to emphasize the importance of moving more. Participants will be asked to fill out questionnaires on course delivery, content and effect throughout the program and 2-3 recorded interviews throughout the study. We will collect measurements of physical performance before and after the program.

NCT ID: NCT02754453 Withdrawn - Weight Loss Clinical Trials

Weight Regain Study After Bariatric Surgery-A Pilot Project

Start date: July 2013
Phase: N/A
Study type: Interventional

There are three different phases to this study: 1. Screening phase to determine if you are eligible to participate in the study. 2. Study phase, which will entail diet and activity, exercise and then finally self monitoring goals. 3. End of treatment phase where you will be asked to complete questionnaires.

NCT ID: NCT02259673 Recruiting - Activity Clinical Trials

Effects of Fun Physical Activity on the Interest to Daily Physical Activity and Sarcopenia of Elderly People

Start date: September 2014
Phase: Phase 1/Phase 2
Study type: Interventional

In this research, the elderly living in nursing homes were selected in two group control and intervention. Intervention group 3 times a week for 20 minutes during 2 months, fun physical exercises (including activities carried out with the use of sports equipment such as beach ball, stretch, bird toys, etc).

NCT ID: NCT01946841 Withdrawn - Quality of Life Clinical Trials

Specific Enteral Nutrition in Malnourished, Dialysis Patients With Chronic Kidney Disease. Efficacy, Safety, Quality of Life

AL-EN-PHED
Start date: August 2013
Phase: Phase 2
Study type: Interventional

The objective of this unblinded study is to assess the nutritional effects of a 12 weeks administration of the specific enteral nutrition (SEN) RealDiet®Renal pockets, as well as the impact on the patients' quality of life.