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NCT ID: NCT06387706 Recruiting - Clinical trials for Chronic Pain Syndrome

The Development of a Gamified Web-based Pain Management Program (GAP) for Community-dwelling Older Adults With Chronic Pain

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

Pain Management in Older Adults: Pain significantly impacts the well-being of older adults, often leading to diminished physical abilities and a reduced quality of life. Despite this, pain management remains suboptimal, with concerns about medication side effects and a tendency to view pain as a natural aspect of aging. Consequently, many seniors are hesitant to use painkillers. As an alternative, non-pharmacological strategies such as educational programs, physical activity, massage, relaxation techniques, and music therapy are gaining traction. Innovative Non-Drug Solutions: To improve participation in non-medication pain relief methods, we suggest incorporating gaming elements into these programs (GAP). Originating in digital media in 2008, gamification has since spread across various industries. It involves adding game-like elements to activities to boost engagement, experience, and motivation. Project Goals: The aims of this initiative include creating a web-based Gamified Pain Management Program (GAP), engaging older adults with chronic pain in the development of GAP, and gathering their feedback on the program's effectiveness.

NCT ID: NCT06386835 Recruiting - Fistula-in-ano Clinical Trials

Collagen Paste vs Mucosal Advancement Flap for FIA

Start date: January 26, 2024
Phase: N/A
Study type: Interventional

The treatment for fistula-in-ano (FIA) remains a challenge to General and Colorectal Surgeons Worldwide. A variety of surgical treatments have been described for high anal fistulas, but none offers the panacea of fistula eradication with guaranteed preservation of continence. This study compares Collagen paste injection to mucosal advancement flap for the treatment of fistula-in-ano.

NCT ID: NCT06385470 Recruiting - Clinical trials for Childhood Apraxia of Speech

Treatment of Cantonese Speakers With Childhood Apraxia of Speech

Start date: April 15, 2024
Phase: N/A
Study type: Interventional

The proposed study aims to investigate the efficacy of the Dynamic Temporal and Tactile Cueing treatment in Cantonese-English bilingual speakers with childhood apraxia of speech.

NCT ID: NCT06383754 Completed - Epiretinal Membrane Clinical Trials

Clareon Intraocular Lens Stability in Vitrectomy Patients: CLOVE Study

Start date: June 7, 2021
Phase: N/A
Study type: Interventional

This prospective randomized controlled trial will be conducted to investigate Clareon intraocular lens (IOL) stability in vitrectomy patients. The investigator plans to target the patients undergoing cataract surgery. A randomized study will be conducted with 2 arms, one with Clareon IOL versus a second arm using the Tecnis 1 In this non-inferiority study, the investigator will compare Clareon IOL from Alcon with the existing Tecnis 1 IOL from Precision Lens which is the commonly used intraocular lens in combined vitrectomy cases in Hong Kong.

NCT ID: NCT06382441 Active, not recruiting - Behavior, Health Clinical Trials

A Tele-exercise Program for Breast Cancer Survivors

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

The research protocol outlines a pilot study for a home-based and group-based tele-exercise program designed for breast cancer survivors. The study is a randomized controlled trial (RCT) led by Dr. Yang Gao from Hong Kong Baptist University, with multiple other investigators from Kwong Wah Hospital and the university itself. Breast cancer is identified as the most prevalent cancer among women globally and in Hong Kong. The document states that adjuvant therapies post-surgery, such as radiation and chemotherapy, can have both short-term and long-term side effects, which may affect the survivors' physical and mental health. The study is based on evidence that physical activity levels often decrease after a breast cancer diagnosis and that exercise can mitigate the side effects of treatment, improving health and quality of life. The pilot aims to test the acceptability and feasibility of a 12-week tele-exercise program that combines psychological theories and behaviour change techniques, transitioning from supervised to unsupervised exercise to build sustainable exercise habits. The study will enrol 24 patients, randomly assigning them to an intervention group or an active control group. The intervention group will receive 12 online training sessions plus 4 psychological counselling sessions, whereas the control group will receive educational essays on exercise and health. The training sessions for the intervention group will include various exercises with increasing intensity and duration over the 4 weeks, monitored by a pulse oximeter to ensure exercises are done at the appropriate heart rate. The sessions will be led by qualified coaches, with Dr. Gao overseeing quality control.

NCT ID: NCT06382363 Recruiting - Diabetes Mellitus Clinical Trials

Improving T2DM Detection Using Spot cHbA1c Test - a Cluster RCT

DM-REACH
Start date: June 11, 2022
Phase: N/A
Study type: Interventional

Objectives: To evaluate the effectiveness of active opportunistic screening using point-of-care capillary Hemoglobin-A1c (POC-cHbA1c) testing, compared to venous HbA1c (vHbA1c) testing, in improving detection of type 2 diabetes mellitus (T2DM) among at-risk primary care patients. Design: Pragmatic cluster randomized controlled trial. Setting: 8 public primary care clinics in Hong Kong. Participants: A minimum of 776 patients (97 per clinic) who have ≥1 risk factor for T2DM, but no known diagnosis of DM or DM screening in the past 12 months. Intervention: Participants at intervention clinics (n=4) will be offered free POC-cHbA1c testing on-site, immediately informed of test results and DM risk, and scheduled for confirmatory oral glucose tolerance test (OGTT) if screened positive (i.e. HbA1c≥5.6%). Participants at control clinics will be offered free vHbA1c testing scheduled on a separate day, informed of test results and DM risk via phone, and scheduled for confirmatory OGTT if screened positive. Main outcome measures: Primary outcomes are uptake rate of POC-cHbA1c versus vHba1c testing, and difference in proportion of T2DM detected between intervention and control groups. Secondary outcomes include number-needed-to-screen to detect one more T2DM case. Data analysis: Participants' characteristics and test uptake rates will be summarized by descriptive statistics. Difference in the proportion of T2DM detected between groups will be compared using Chi-squared test. Number-needed-to screen to identify one additional patient with DM will be calculated. Expected results: A greater proportion of T2DM patients will be detected by POC-cHbA1c than vHbA1c due to a higher screening test uptake rate among the studied population.

NCT ID: NCT06380023 Completed - Airway Aspiration Clinical Trials

An Investigation Into the Dispersion Pattern During Coughing and Open Nasopharyngeal Suction Using Various Barrier Devices

Start date: September 1, 2022
Phase:
Study type: Observational

The aim of the study is to examine the air dispersion pattern and the environmental influence of open airway suction in general ward setting. Secondly, the study is aimed at identifying a simple & practical enclosure device in general ward. Suction will be performed in manikin in supine lying. Nasopharyngeal suction will be performed by physiotherapist with working experience more than 1 years. Besides, surgical mask & enclosure tent will be adopted as the enclosure barrier device in this study. Research Question 1. To assess the extent of the environmental contamination during coughing and simulated airway suction 2. To measure the air particle count during coughing and simulated open airway suction. 3. To evaluate how effective the enclosure barrier in reducing the air particle dispersion during open airway suction.

NCT ID: NCT06378164 Recruiting - Clinical trials for Older Adults With a History of Falls

The Effect of Combined Volitional and Reactive Step Training in Reducing Falls Risk in Older Fallers

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

To examine the immediate and sustained effect of a 4-week combined volitional and reactive step training on fall risks in community-dwelling older fallers.

NCT ID: NCT06377124 Not yet recruiting - Lung Cancer Clinical Trials

A Smart Self-Management Support Programme (3S) to Improve Quality of Life in Lung Cancer Patients

Start date: April 22, 2024
Phase: N/A
Study type: Interventional

Lung cancers patients often experience multiple symptoms (e.g. fatigue, dyspnea, distress, depression, sleep disturbance). The current study attempts to explore the efficacy of the Smart Self-Management Support Programme (3S) in improving quality of life of patients using self-management support programme with mobile devices.

NCT ID: NCT06376864 Active, not recruiting - Child Behavior Clinical Trials

Physical Activity Intervention Effects on Executive Function, Physical Activity and Sedentary Behaviour in Children

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

The current study aims to implement the Activity Breaks intervention and evaluate its effectiveness on outcome measures of executive function (EF), physical activity (PA), and sedentary behaviour (SB) in school children.