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NCT ID: NCT05441735 Recruiting - Long-term Care Clinical Trials

The Effectiveness of Digital Care-plan for Improving Long-term Care 2.0 Service Activation Proportion

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

Digital tools can potentially improve the public's reception to and understanding of long-term care information, which will be significantly helpful for long-term care workers and effectively increase the coverage provided by long-term care services. The results of this study could be used to further explore the feasibility of service digitization in the field of long-term care, as well as the integration of technology and professional knowledge to facilitate access to long-term care resources in a modern setting.

NCT ID: NCT05441137 Not yet recruiting - Clinical trials for Young Children With Motor Disabilities

Using Head-mounted, Eye-tracking to Compare Looking, Manual Exploration and Social Interaction During Active Locomotion

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

The three purposes of this study are: 1) to determine the feasibility of using a head-mounted eye-tracker and examine the effects of the optimal mobility training on increasing visual and manual exploration in toddlers with different severity levels of motor delays, 2) to compare the effectiveness of providing optimal mobility training on outcomes across the ICF framework in toddlers with mild, moderate and severe motor delays, and 3) to determine the effects of optimal mobility training on the relationship among looking and manual actions, caregiver-child interactions and mastery motivation in toddlers with mild, moderate and severe motor delays. Based on the power analysis from the preliminary results of the pilot study, we will recruit 72 toddlers with motor delays and further assign them to the mild, moderate or severe motor delays group. The participants in each group will be randomly assigned to either the ROC training program or conventional therapy (Control) program, resulting the following six training groups: the ROCStand(Mild) group (n=12), the ROC-Stand25(Mod) group (n=12), the ROCSit(Sev) group (n=12), Control(Mild) group (n=12), Control(Mod) group (n=12), and Control(Sev) group (n=12). The whole study duration will be 24 weeks, including a 12-week intervention and a 12-week follow-up. All programs will include 120 minutes/per session, 2 sessions/per week. Participants will continue their regular therapy during the whole study. The head-mounted cameras worn by the participants and caregivers will record the visual and manual behaviors for 40 minutes/per week during intervention. Standardized assessments are provided for a total three times, including the time before and after the intervention and in the end of the follow-up phase. Assessments include body function, mobility, psychosocial function, family perception and participation. The findings of this study will provide guidelines for arranging the training environment depending on each child's and family's needs.

NCT ID: NCT05440227 Recruiting - Clinical trials for Cancer-related Fatigue

PG2 Injection for the Treatment of moderate-to Severe Fatigue in Breast Cancer Patients

Start date: June 15, 2022
Phase: Phase 2
Study type: Interventional

The objective of this study is to assess the efficacy of weekly PG2 regimen as a complementary treatment for patients with recurrent unresectable (local or regional) or metastatic breast cancer who experienced moderate to severe fatigue while receiving chemotherapies.

NCT ID: NCT05439889 Not yet recruiting - Clinical trials for Chronic Myeloid Leukemia, BCR/ABL-Positive

Follow-up Study on Chronic Myeloid Leukemia Patients Achieving Treatment-free Remission

Start date: June 24, 2022
Phase:
Study type: Observational [Patient Registry]

In recent years, the goal of stopping drug therapy, also known as treatment-free remission (TFR), is emerging as one of the management goals of chronic myeloid leukemia (CML) therapy. Because there is no available data on Asian patients with CML undergoing tyrosine kinase inhibitor discontinuation (TKI), the investigators plan to recruit chronic phase CML patients with deep treatment response and good medical compliance in Taiwan to evaluate the feasibility, safety and clinical consequences of TKI discontinuation.

NCT ID: NCT05439876 Recruiting - Clinical trials for Epilepsy in Children

Getting SMART for Pediatric Epilepsy

Start date: July 1, 2022
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to evaluate the effect of melatonin for improving sleep in pediatric epilepsy.

NCT ID: NCT05439343 Active, not recruiting - Analgesia Clinical Trials

Adductor Canal Block and Multimodal Local Infiltration Analgesia in Patients Receiving Total Knee Arthroplasty

Start date: October 15, 2018
Phase: N/A
Study type: Interventional

Total knee arthroplasty (TKA) is associated with moderate to severe pain after operation. There are twenty thousand patients undertaking TKA annually in Taiwan, and the average length of hospital stay is about seven to ten days. In contrast, the length of hospital stay is only three to six days in some literatures. Adequate pain relief after surgery allows patients to mobilize earlier and easier and rehabilitate to reduce the length of hospital stay. By reducing hospital stay, we can reduce medical expenditure of national health insurance. In addition, effective analgesia can reduce the occurrence of chronic post-surgical pain which would compromise life quality and produce socioeconomic problems. This study tries to find a better solution for postoperative analgesia of TKA for patients in Taiwan. The present clinical study compares the effect of adductor canal block and local infiltration on postoperative analgesia and functional activity after TKA. To assess the outcome of both methods in the same patient, we can have more comparative result of pain score and functional parameters like range of motion of knee joint, time and ability to ambulate. Based on that, we try to find a better option for postoperative analgesia for patients receiving TKA in Taiwan.

NCT ID: NCT05439317 Completed - Knee Osteoarthritis Clinical Trials

Elasticity of the Hoffa's Fat Pad in Patients With Knee Osteoarthritis

Start date: December 3, 2021
Phase:
Study type: Observational

Knee osteoarthritis (OA) is a common problem in clinical settings. Knee OA is well known for its association with the wear and tear of the cartilage and osteophyte formation. Evidence has suggested the importance of the infrapatellar fat pad, known as Hoffa's fat pad, during the development of knee OA. Some studies have demonstrated the protective role of the infrapatellar fat pad, whereas others have suggested an inflammatory role such as increased fibrosis and proinflammatory cytokine levels. Ultrasound is exceptionally convenient in the assessment of the musculoskeletal system, and elastography is a tool to evaluate tissue texture. Therefore, in this study, we investigated the Hoffa's fat pad in knee OA patients by using elastography.

NCT ID: NCT05439122 Not yet recruiting - Clinical trials for Biomechanical Phenomena

Trunk and Shoulder Muscle Performance in Volleyball Players With Shoulder Pain

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

Volleyball players repetitively place the arm into extreme positions, and thus expose the athletes' shoulders to a large load and increase the risk of injuries. The shoulder complex is identified as one of the most injured joints in volleyball sports. Although many studies have revealed alterations in the function, morphology and biomechanics of the shoulder complex in volleyball players with shoulder pain, some researchers suggested that a smooth energy transfer from the axial skeleton, through the shoulder complex, to the arm and hand is crucial for overhead sports performance and injury prevention, with little evidence showing the link between trunk muscle performance and shoulder pain in volleyball players. Therefore, the main purposes of present study are (1) to compare the trunk muscle performance (muscle strength, power and endurance) in volleyball players with and without subacromial impingement syndrome (SIS); (2) to compare trunk and shoulder muscles activity during spiking in volleyball players with and without SIS.

NCT ID: NCT05438251 Not yet recruiting - Clinical trials for Diabetic Foot Ulcer (DFU)

Exploring the Effect of Fespixon Cream for the Treatment of Diabetic Foot Ulcers (TEXAS 3A, 3B)

Start date: July 1, 2022
Phase: Phase 4
Study type: Interventional

A Research Study to evaluate the therapeutic effect of Fespixon cream in patients suffering from DFU (UTWCS Grade III-A or III-B) by measuring the change of grade of UTWCS (University of Texas Diabetic Wound Classification system), wound area reduction, infection control, and incidence of treatment-emergent adverse event (TEAE).

NCT ID: NCT05437887 Not yet recruiting - Atopic Dermatitis Clinical Trials

Effects of Fucoidan on the Gut Microbiota in the Patients of Atopic Dermatitis

Start date: July 30, 2022
Phase: N/A
Study type: Interventional

Forty patients with physician-identified atopic dermatitis will be enrolled in the study. All patients must be aged between 6 and 60 years old. All patients consumed fucoidan for 3 months.