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NCT ID: NCT05772949 Completed - Technology Clinical Trials

Effectiveness of a Smart Hearing Aid on Improving Psychosocial Well-being in Elderly

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

The study has 2 primary research questions, 4 secondary research questions, and 2 auxiliary research questions targeting elderly with hearing impairment. The research questions are: Primary study questions: 1. Can the use of the smart hearing aids reduce loneliness at the end of intervention? 2. Can the use of the smart hearing aids improve quality of life at the end of intervention? Secondary study questions: 3. Can the use of the smart hearing aids improve the communication quality between caregivers and participants at the end of intervention? 4. How is the satisfaction of the participants with the smart hearing aids? 5. What are the factors leading to the use and non-use of the smart hearing aids? 6. What is the usage time of the smart hearing aids? Auxiliary study questions: 7. How is the caregiver burden when facilitating the participants to use the smart hearing aids? 8. What are the perceived benefits and acceptability of the smart hearing aids?

NCT ID: NCT05729087 Completed - Physical Activity Clinical Trials

Development of a Blended Lifestyle Intervention to Promote Physical Activity, Diet, and Health in Hong Kong Older Adults

Start date: June 14, 2022
Phase: N/A
Study type: Interventional

This pilot study will provide a theory-based low-cost and easy-to-operate program in the area of healthy lifestyle promotion among community dwelling older adults. The blended intervention product will be helpful for health professionals, social workers and practitioners working in the elderly centers and health centers to promote older adults' PA, healthy diet and wellness. Furthermore, this study would initiate advocacy for policymakers to disseminate cost-saving, time-efficient and effective healthy lifestyle programs to the communities for healthy aging promotion.

NCT ID: NCT05710471 Completed - Clinical trials for Age-Related Macular Degeneration

Treatment of Recalcitrant Neovascular AMD Using Brolocizumab With Immediate T&E

Start date: July 25, 2022
Phase: Phase 4
Study type: Interventional

The investigator propose to conduct a randomized clinical trial, investigating the safety and efficacy of brolucizumab for treatment of nAMD patients with CNV, and plans to specifically target those who are not responding to standard Treat and Extend (T&E) treatment. A randomised omized study will be conducted with 2 arms, one with the new drug (brolocizumab) and novel treatment protocol versus a second arm using the current gold standard of aflibercept and the T&E protocol

NCT ID: NCT05710458 Completed - Retinal Detachment Clinical Trials

Performance Comparison of the 25 Gauge 20,000cpm HYPERVIT Dual Blade vs. 10,000cpm ULTRAVIT Vitrectomy Cutter

Start date: July 1, 2021
Phase: N/A
Study type: Interventional

This prospective randomised controlled trial will be conducted to investigate that increasing the vitrectomy cutting rate from 10,000 cut/min to 20,000 cut/min will result more efficiency and shorter core vitrectomy time, and it is equally safe as compared to the current 10,000 cut/min. We plan to target the patients undergoing for vitrectomy for common vitreoretinal pathology. Our plan is to conduct a randomised study with 2 arms, one with the higher cutting rate (20,000 cut/min) versus a second arm using the existing system 10,000 cuts/min.

NCT ID: NCT05694507 Completed - Mental Well-being Clinical Trials

Evaluation of Chatbot for Mental Well-being

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

The present study consists of two two-armed randomized controlled trials between experimental and waitlist control groups. It aims to evaluate the effectiveness of conversational chatbot in improving mental health literacy, uptake of self-care behaviors, and mental well-being, compared to the waitlist control, and the effectiveness of daily notification on adherence. This study will provide important findings for the future development and implementation of chatbots in mental health, which may increase public access to immediate mental health support. It is hypothesized that participants in the experimental condition will show (H1) better mental health literacy (H2) better improvement in self-care and self-efficacy in mental well-being, and (H3) better mental well-being, compared with participants in the control condition. Also, it is hypothesized that participants with daily reminders will show (H4) a better adherence rate in using chatbot compared with participants without daily reminders

NCT ID: NCT05688150 Completed - Osteoporosis Clinical Trials

Prevalence and Associated Factors of Sarcopenia Among Elderly Patients in Osteoporosis Clinic

Start date: June 20, 2022
Phase:
Study type: Observational

This was a cross-sectional study. Patients who attended the osteoporosis clinic of Kowloon Hospital from June to December 2022 were recruited. Grip strength and appendicular skeletal muscle mass index were measured with a Jamar dynamometer and a bioimpedance analyser. Since most patients in our clinic are of Chinese ethnicity, the diagnostic criteria in the Consensus Update on Sarcopenia Diagnosis and Treatment by the Asian Working Group for Sarcopenia in 2019 was utilised. The diagnosis of sarcopenia was established by the presence of both low grip strength (Male: < 28 kg, Female < 18 kg) and low appendicular skeletal mass (Male: < 7.0 kg/m2, Female: < 5.7 kg/m2)

NCT ID: NCT05686304 Completed - Clinical trials for Severe Mental Illness

Effectiveness of Internet-based Self-help Money Management Program Among Adult With Severe Mental Illness

Start date: September 1, 2022
Phase: N/A
Study type: Interventional

This experimental study aims to develop an internet-based self-help money management program that improve financial self-efficacy and its associated adverse outcomes among adult population with severe mental illness. In particular, this study compares the efficacy of the internet-delivered self-help money management program with the wait-list control group. The online money management program course will consist of 4 weekly modules, incorporating the key components of money management and the Model of Human Occupation (MOHO). The program include the concept of money management, money management skill, and risk of financial exploitation. The main component of each module will be presented in video format, quiz, and homework. Materials will be presented interactively to facilitate engagement.

NCT ID: NCT05686291 Completed - Healthy Volunteer Clinical Trials

Effectiveness of Hybrid Learning Mode of Volunteer Training

Start date: August 1, 2022
Phase: N/A
Study type: Interventional

As the effectiveness of the hybrid volunteer training in Hong Kong is under-studied, this experimental study aims to develop a hybrid learning mode of volunteer training that increase volunteering-related self-efficacy and its associated outcomes among volunteer. In particular, this study compares the efficacy of hybrid volunteer training with the wait-list control group. The volunteer training will consist of a 6-module online course, followed by 5 face-to-face courses. Each module will consist of the key volunteer training component presented in in written or video format. Materials will be presented interactively to facilitate engagement.

NCT ID: NCT05678972 Completed - Mindfulness Clinical Trials

Pause and Breathe: Online Self-Help Mindfulness-Based Intervention: Investigation of Its Efficacy and Mechanism of Change

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

The current study aims to evaluate the effectiveness of a 4-week self-help online mindfulness-based intervention on mental and physical well-being in comparison to the waitlist control group. This study can provide support to the utility of self-help online mindfulness-based intervention, which may advance our understanding of the causal pathways between mindfulness-based intervention and well-being and guide future research. It is hypothesized that participants in the experimental condition will show better mental well-being, physical well-being, and better improvement in mindfulness and related attributes compared with participants in the control condition. Upon completing the screening and pre-evaluation questionnaire, participants will be randomly assigned to either mindfulness group or waitlist control group. They will complete three sets of questionnaires in total which will be administered before the intervention (pre-test assessment), right after the 4-week intervention (post-test assessment), and four weeks after the intervention (follow-up assessment), respectively. In the experimental group, participants in the mindfulness group will engage in a 4-week online mindfulness course. The self-help online mindfulness course includes education about mindfulness, guided meditations (e.g., mindful breathing, mindful eating, mindful walking, body scan, acceptance, choiceless awareness and disengaging from thoughts exercise), and guidance on using informal mindfulness skills in day-to-day life. Readings, audio and videos are included to explain the concept of mindfulness and overcome common difficulties associated with mindfulness practice. In the waitlist control group, participants are to refrain from access the online course until they finished the follow-up questionnaire. All participants will be able to access the materials in an online platform after they have completed the research.

NCT ID: NCT05671354 Completed - Technology Clinical Trials

The Acceptability of Auto-wrapping Commode Chair in Elderly Residential Setting

Start date: March 5, 2023
Phase: N/A
Study type: Interventional

The study has 4 research questions regarding the use of auto-wrapping commode chairs in elderly residential setting: Primary study questions: 1. Can the frequency of the spills of excretions during disposing of excretions be reduced when auto-wrapping commode chairs are used as compared to conventional commode chairs? Auxiliary study questions: 2. Can the staff time spent on disposing of excretions from commode chairs be reduced when auto-wrapping commode chairs are used as compared to conventional commode chairs? 3. What is the satisfaction of the residents and staff on using the auto-wrapping commode chairs? 4. What are the perceived benefits and feasibility in allowing the residents to use the auto-wrapping commode chairs?