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Older People clinical trials

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NCT ID: NCT05859737 Not yet recruiting - Older People Clinical Trials

Disaster Preparedness of Older People

SIMAH
Start date: October 1, 2023
Phase: N/A
Study type: Interventional

Disasters; It is an important public health problem of uncertain time, causing loss of life and property, having severe economic consequences, and causing serious health problems in the long term. In dealing with disasters, it is expected that measures to reduce the damage and losses caused by the hazards that the disaster may cause are taken during the disaster preparedness phase. For this reason, the individuals in the society should be educated before the disaster and their preparedness for the disaster should be ensured. While it is possible for young age groups to access information, participate in public education and self-learning, they need support for their preparedness for disasters because there is no disaster education program specific to older individuals. This project was designed as a single-blind (participant) randomized controlled study in order to examine the effect of the Disaster Preparedness Education Program (SIMAH) based on the Health Belief Model of older people in the society on their preparedness to disasters according to the active control group to which the public education materials prepared by the Disaster and Emergency Management Presidency (AFAD) will be given. The research was planned to be carried out in a total of six clusters in Antalya province Muratpaşa district and Konyaaltı district between October and December 2023 in older people houses, retirement cafes and district parks where older people are concentrated. The sample size was calculated as 66 older individuals (intervention: 33, control: 33). The SIMAH Program, which includes interactive group training for three months, public education materials prepared by AFAD, and reminder phone messages, will be applied to the initiative group. Public education materials prepared by AFAD will be given to the active control group in the same period. Outcomes will be measured with the Disaster Readiness Scale, the General Disaster Preparedness Belief Scale, and the Individual Disaster Preparedness Evaluation Form, before the intervention, after the training program, and three months later.

NCT ID: NCT05803460 Recruiting - Older People Clinical Trials

Explore the Effects of Virtual Reality Natural Environment of Older People

Start date: April 7, 2023
Phase: N/A
Study type: Interventional

The purpose of this study is to develop and explore the effects of virtual reality based natural environment intervention programs on improving attention, emotion, and cognitive function of older people. The study has three stage. The first stage is to develop and verify the effects of virtual natural environment on attention recovery and emotional recovery of institutional elders. The second stage is to evaluate the attention recovery and emotional effects of different types of virtual natural environments on institutional elders. The third stage is to test effects of the virtual natural environment intervention program improved attention, cognitive function, anxiety and depression in the institutionalized elders compared with the control group.

NCT ID: NCT05626556 Completed - Frailty Clinical Trials

A Technology-based Intervention to Support Older Adults in Living Independently

SAVE
Start date: October 17, 2022
Phase: N/A
Study type: Interventional

The general objective of this study is to test the usability and efficiency of the SAVE prototype, a technology-based support for enabling older adults to keep their independent and active lives in their homes and maintain their social relationships for as long as possible.

NCT ID: NCT05606510 Recruiting - Back Pain Clinical Trials

The Effects of Mindful Exercise on Back Pain in Older Patients With Primary Osteoporosis

Start date: February 16, 2023
Phase: N/A
Study type: Interventional

The goal of this randomized control trial is to determine the effects of a mindful exercise program on physical (back pain and balance) and psychological (mindfulness, kinesiophobia, anxiety and depression) consequences of primary osteoporosis in older patients. The main questions it aims to answer are: - What are the levels of pain, balance, mindfulness, kinesiophobia, anxiety and depression in older patients with primary osteoporosis? - Are there differences in pain, balance, mindfulness, kinesiophobia, anxiety and depression according to sociodemographic-clinical characteristics of the patients? - Are there differences in pain, balance, mindfulness, kinesiophobia, anxiety and depression between the intervention (mindful exercise) and control (usual care) groups of older patients with primary osteoporosis? 128 participants who meet the criteria will be recruited from the pain department of a Tertiary A level provincial Traditional Chinese Medicine hospital in Mainland China, and randomly assigned to the intervention group or control group. All patients in both groups will receive usual care, including routine medicine and nursing care. The study will last for 12 weeks (one-week training in hospital and 11-week on-line sessions at home) and 4-week follow up. Patients in the intervention group will receive a group-based mindful exercise which will be conducted 5 times per week, 30 minutes per session, and co-led by a mindfulness-trained main researcher and a professional exercise specialist for the first week (week 1) hospitalization. When they discharge, on-line sessions (week 2-12) will be conducted by the main researcher from Monday to Friday. Patients and primary caregivers will be taught how to use 'Tencent meet' software. Upon discharge, a WeChat group will be set up to notify the exercise time and send the links for the online sessions. Those in the control group will received routine medicine and nursing care as usual, and only be taught on the hospital-recommended movements (physical stretching) and encouraged to do it at home on their own. All the variables (pain, mindfulness, kinesiophobia, anxiety and depression) and the TUG test (balance) will be measured at the following time point: baseline (Time 1), week 4 (Time 2), week 8 (Time 3), week 12 (Time 4, immediately post-intervention) and week 16 (Time 5, 4 weeks after the intervention) for the two groups of patients. The study will obtain ethical clearance from the study setting, as well as written consent from the participants. Descriptive statistics will be computed for all variables. Normality and homogeneity of the variances will be tested using the Shapiro-Wilk and Levene tests, respectively. The data will be analyzed using mixed-model analysis of variance to test the main and interaction effects of group (independent factor) and time (repeated-measures factor) on the dependent variables. The findings of the study would certainly have implications for the treatment of older patients with primary osteoporosis, especially non-pharmacological treatment.

NCT ID: NCT05543538 Completed - Older People Clinical Trials

Influence of Different Teaching Strategies on the Academic Performance and Caring of Nursing Students

Start date: March 3, 2022
Phase: N/A
Study type: Interventional

The participants in this study are college students with studying long-term care. After different teaching strategies, the students are hypothesised to improve their caring ability in the future and apply rhythmic muscle training programmes. Therefore, this study will explore the relationship amongst three different teaching strategies of nursing students through multimedia audio-visual, multimedia audio-visual and experiential learning programmes and teachers' personal demonstration and experiential learning, as well as identify their relationship with caring ability.

NCT ID: NCT05532371 Completed - Older People Clinical Trials

The Effect of Exercise on Cognitive Status in Older Adults

Start date: January 30, 2019
Phase: N/A
Study type: Interventional

The purpose of the study is to demonstrate the effectiveness of the different combinations of exercises on the cognitive status of older adults with cognitive decline.

NCT ID: NCT05395676 Recruiting - Older People Clinical Trials

Cognitive Exergame Training on Dual-Task Cost and Balance Stability in Older Adults

Start date: April 11, 2022
Phase: N/A
Study type: Interventional

Balance stability requires both motor and cognitive (mental) functions working together. Balance stability may decrease when performing two tasks at the same time (dual task), as cognitive and motor tasks compete for performing a higher task. Meanwhile, social distance and remote working become a necessity due to Covid-19. The primary aim is to evaluate the feasibility of cognitive exergame training in reducing dual-task costs and improve the balance performance among individuals between 65 and 85 years. The secondary aim is to observe the effectiveness of virtual home exercise on adherence and interactive rate of the population between 65 and 85 years.

NCT ID: NCT05367128 Recruiting - Healthy Clinical Trials

Effects of Dual Task Prioritization Training on Dual Task Walking in Older People

Start date: July 25, 2022
Phase: N/A
Study type: Interventional

The purpose of this single-blinded three-armed randomized controlled trial is to investigate the effect of different task prioritization during dual task training on dual task performance.

NCT ID: NCT05241886 Completed - Sarcopenia Clinical Trials

Evaluation of Sarcopenia With SARC-F and Anthropometric Measurement

Start date: July 1, 2018
Phase:
Study type: Observational

The aim of this study is to examine the performance of determining the sarcopenia by anthropometric measurements (mid-upper arm circumference and calf circumference) added to the SARC-F questionnaire developed as a screening tool for the risk of sarcopenia in the community-dwelling older adults. The risk of sarcopenia of the individuals over 65 years of age who applied to the Geriatrics Department of Ege University Medical Faculty Hospital Internal Diseases Department. was determined by the SARC-F questionnaire, muscle mass was established by bioelectrical impedance analysis, muscle strength was assessed by handgrip strength, physical performance was assessed by a 4-meter walking test and presence of malnutrition was assessed with an MNA-long form. For the diagnosis of sarcopenia; old (EWGSOP 1) and revised (EWGSOP 2) diagnostic criteria of Sarcopenia Study Group in Elderly Individuals of the European Union Geriatric Medicine Association were used. New parameters were obtained by adding calf circumference (SARC-CC) and mid-upper arm circumference (SARC-MUAC) measurements were added separately and together (SARC-CC-MUAC) to the SARC-F. For the calf circumference cut-off points of <31 cm and <33 cm and for the mid-upper arm circumference cut-off points of <25 cm and <31 cm were used for the sensitivity and specificity analyses.

NCT ID: NCT05193773 Completed - Intervention Clinical Trials

Effects of a Multifactorial Intervention to Reduce Physical Restraints for Care Providers in Nursing Homes

Start date: September 7, 2015
Phase: N/A
Study type: Interventional

Scholars from around the world have been strongly advocating restraint-free care in long-term care institutions. Therefore, the aim of this study was to evaluate the effects of a multifactorial intervention to reduce physical restraints for care providers in nursing homes.