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NCT ID: NCT05540236 Completed - Clinical trials for Laparoscopic Surgery

Effects of Auricular Acupressure on the Management of Postoperative Nausea and Vomiting After Gynecological Laparoscopic Surgeries

Start date: July 18, 2021
Phase: N/A
Study type: Interventional

Auricular acupressure is easily accessible and easily performed, and can significantly relieve PONV symptoms, and improve patient's satisfaction in women receiving general anesthesia for gynecological surgeries. This makes it an economically-beneficial supplemental therapy, worthy of promoting for patients receiving general anesthesia.

NCT ID: NCT05537870 Completed - Neoplasms Clinical Trials

The Effectiveness of Nurse Navigators in Cancer Care

Start date: January 17, 2019
Phase: N/A
Study type: Interventional

Cancer patients will be recruited from the Taipei Cancer Center of Taipei Medical University. This study was divided into two phases. The first phase adopted cross-sectional study design with questionnaires to analyze the potential predictors of depressive symptoms among cancer patients. The second stage was adopted experimental study design to explore the effectiveness of nurse navigators in cancer care.

NCT ID: NCT05533788 Completed - Health, Subjective Clinical Trials

ABSK091 Food Effect Study in Healthy Subjects

Start date: September 8, 2020
Phase: Phase 1
Study type: Interventional

In this study, a single oral dose of the tablet formulation administered under fed conditions will be compared to administration under fasted conditions to assess the effects of a high-fat meal on the rate and extent of absorption and exposure. Study ABSK091-101 is a single-center, Phase 1, open-label, randomized, two-period, two-sequence, and crossover study in healthy subjects.

NCT ID: NCT05524818 Completed - Stroke Clinical Trials

Validations of the Computerized Adaptive Testing System of the Functional Assessment of Stroke

Start date: April 14, 2021
Phase:
Study type: Observational [Patient Registry]

Purposes: The aim of this study is to preliminarily validate the test-retest reliability, random measurement error, practice effect, and responsiveness of the the Computerized Adaptive Testing System of the Functional Assessment of Stroke (CAT-FAS) in real clinical settings. Methods: Patients in both chronic (get stroke over 6 months) and sub-acute (get stroke less than 6 months) stages will be recruited. These patients will be classified into "test-retest reliability group" and "responsiveness group" to examine the test-retest reliability and responsiveness of the CAT-FAS, respectively. All participants will receive the administrations of CAT-FAS twice. For those in the test-retest reliability group, the administrations will be performed with a 4-week interval. For those in the responsiveness group, the administrations will be performed at admitting to the rehabilitation unit and before they are discharged.

NCT ID: NCT05521347 Completed - Caffeine Clinical Trials

Caffeine Supplementation Improves the Cognitive Abilities and Shooting Performance of Trained E-sports Players

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

Purpose: investigators explored the effect of 3 mg/kg of caffeine supplementation on the cognitive ability and shooting performance of trained e-sports players. Methods: investigators recruited nine e-sports players who had received professional training in e-sports and had won at least eighth place in national-level e-sports shooting competitions. After performing three to five familiarization tests, investigators employed a randomized crossover design to divide participants into a caffeine trial (CAF) and a placebo trial (PL). The CAF group took capsules with 3 mg/kg of caffeine, whereas the PL group took a placebo capsule. After a 1-h rest, the Stroop task, visual search ability test, and the shooting ability test were conducted.

NCT ID: NCT05519280 Completed - Quality of Life Clinical Trials

Effects of a Biopsychosocial-Spiritual Group Intervention on Quality of Life of Institutionalized Seniors

Start date: January 1, 2019
Phase: N/A
Study type: Interventional

This study aimed to evaluate the effects of a biopsychosocial-spiritual (BPS-S) Group intervention on quality of life among seniors with disabilities in long-term care residential settings.

NCT ID: NCT05517460 Completed - Schizophrenia Clinical Trials

The Efficacy of Auricular Acupressure on Improving Constipation Among Residents in Community Rehabilitation Center

Start date: September 6, 2022
Phase: N/A
Study type: Interventional

The purpose of the study is to examine the effect of auricular acupressure on improvement of constipation and heart rate variability among residents with schizophrenia in community rehabilitation Center.The hypothesis of this study is that residents with schizophrenia in Community Rehabilitation Center receiving auricular acupressure can improve the symptoms of constipation and heart rate variability.By identifying the effectiveness of auricular acupressure can reduce the occurrence of constipation; suitable care can be suggested to improve gastrointestinal health in residents of Schizophrenia in community rehabilitation center.

NCT ID: NCT05517395 Completed - Stunting Clinical Trials

The Effectiveness of HBM-based Education Program on Improve Knowledge and Behaviors

Start date: September 10, 2022
Phase: N/A
Study type: Interventional

The randomized controlled trial design with one intervention arm (nutrition education and complementary feeding) and one control (usual care) arm (1:1 ratio). Randomization of each participant to the groups will be carried out using Random Allocation Software 1.0 (https://random-allocation-oftware.software.informer.com/1.0/) to intervention or control groups in a 1:1 ratio. The sample size to be recruited is 80 participants.

NCT ID: NCT05514197 Completed - Postoperative Pain Clinical Trials

The Impact of Intravenous Vitamin C Combined With Nerve Blocks on Postoperative Pain and Recovery After Total Knee Arthroplasty

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

The aim of this prospective randomized-control study was to evaluate the impact of a single high-dose intravenous vitamin C added to ultrasound-guided blocks at induction on postoperative pain, sngception and early functional rehabilitation of the knee joint in patients under-going total knee arthroplasty.

NCT ID: NCT05510635 Completed - Pediatric Cancer Clinical Trials

The Effectiveness of Bibliotherapy on Emotional Distress, Coping Strategies and Resilience of Adolescents With Cancer

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

Adolescents with cancer who were diagnosed within two years suffered severe emotional distress. Bibliotherapy therapy uses healing materials as a medium to enable individuals experiencing emotional distress to obtain emotional healing through story situations, thereby enhancing resilience. However, there is a lack of research on bibliotherapy in adolescents with cancer. Therefore, the investigators would like to evaluate the effectiveness of interactive bibliotherapy in improving emotional distress and coping strategies and enhancing the resilience of adolescents with cancer compared to reading bibliotherapy.