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NCT ID: NCT06216236 Completed - Virtual Reality Clinical Trials

Effects of Physical Fitness Using a Kinect Interventional System

Start date: January 1, 2020
Phase: N/A
Study type: Interventional

The Kinect intervention system combined with aerobic exercise training can improve the quality of life of older adults in the community, standardize behavior regulation in exercise and improve fitness enthusiasm. Aerobic exercise training using the Kinect intervention system was more effective than traditional training

NCT ID: NCT06208475 Completed - Appetitive Behavior Clinical Trials

Different Menstrual Cycle in Eating Behavior Following Resistance Exercise

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

The study aims to provide insights into how menstrual cycle phases impact appetite responses to resistance exercise in young women. Healthy young women will participate in four trials: the exercise session in the follicular phase, the exercise session in the luteal phase, the control session in the follicular phase, and the control session in the luteal phase. Various measurements will be taken, including subjective appetite perceptions, appetite hormones, food preferences, lactate levels, estradiol levels, progesterone levels, and energy intake.

NCT ID: NCT06206798 Completed - Quality of Life Clinical Trials

Resourcefulness Group Intervention on Recovery and Quality of Life

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

The purpose of this study was to test the effects of resourcefulness group intervention on facilitating recovery and improving the quality of life in patients with chronic schizophrenia.

NCT ID: NCT06205173 Completed - Colorectal Cancer Clinical Trials

Explored About Temperature Packing Care to Improve the Quality of Life for Chemotherapy Induced Peripheral Neuropathy (CIPN) in Colorectal Cancer and Gastric Cancer Patient

Start date: August 19, 2020
Phase: N/A
Study type: Interventional

Investigate the effectiveness of cold and hot compress interventions in reducing peripheral neuropathy induced by Oxaliplatin chemotherapy in colorectal cancer and gastric cancer patients. The primary outcome measures include quality of life, and secondary outcome measures encompass the severity of peripheral neuropathy, manual dexterity assessed through finger strength testing, and the effects on microcirculation blood flow in the hands and feet

NCT ID: NCT06199739 Completed - Clinical trials for Bony Weight Bearing Disorder

Safety of Immediate Weight-Bearing as Tolerated After Well-Reduced Geriatric Hip

Start date: January 1, 2020
Phase: N/A
Study type: Interventional

Purpose: Proximal femur fracture is a major traumatic injury in elderly populations; however, practical postoperative weight-bearing protocols are lacking. Therefore, the purpose of the present study was to investigate whether early weight-bearing status after proximal femur nail fixation is associated with any loss of reduction and evaluate the clinical outcomes of this intervention. Patients and methods: For this prospective single center clinical trial study, we recruited 14 proximal femur fracture cases, classified by AO/OTA 2018, receiving intramedullary nail fixation. Clinical outcomes included the Harris functional hip score and VAS pain score. Additionally, demographic data, radiological parameters, time to weight-bearing, mortality rate, medical and surgical complications, and final ambulation status were recorded.

NCT ID: NCT06199596 Completed - Chronic Insomnia Clinical Trials

Alpha-s1 Casein Hydrolysate on Sleep

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

This study investigates the impact of Aalpha-s1 casein hydrolysate (ACH; Lactium®) on sleep quality in individuals with chronic insomnia, employing both subjective sleep profiles and objective polysomnography (PSG) recordings.

NCT ID: NCT06199323 Completed - Parkinson Disease Clinical Trials

Acupuncture Therapy on Dysphagia in Parkinson's Disease

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

From June 2019 to May 2021, we conducted a randomized controlled study, including dysphagic patients with Parkinson's diseases who were admitted to the department of rehabilitation medicine in 3 hospitals in China. The participants were divided randomly into the experimental group and the control group, with 56 in each one. Both two groups were given routine treatment and swallowing rehabilitation training. Moreover, the experimental group was given acupuncture therapy.

NCT ID: NCT06194487 Completed - Skin Condition Clinical Trials

Efficacy Evaluation of Collagen Drink Products

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

To assess MAXI Collagen drink on skin condition improvement

NCT ID: NCT06188845 Completed - Stroke Clinical Trials

Kinesio Taping in Stroke Patient

Kinesio taping
Start date: January 4, 2021
Phase: N/A
Study type: Interventional

Despite being nearly independent in daily life, chronic high-functioning stroke survivors still experienced mild impairments in skilled hand function. Kinesio Taping (KT) has been used to help stroke patients improve their balance and ambulation. Few studies explored the effects of KT on fine motor function in stroke patients. The purpose of this study was to investigate the hand function performance of high-functioning stroke survivors after KT. Participants were divided into two groups: KT group and control group. Last two days, the KT group received KT intervention. After the taping was removed, baseline and post-test evaluation were conducted. Outcome measures included muscle strength, range of motion (ROM), spasticity, fine motor function, and self-reported upper limb disability. The results revealed that the KT group had less spasticity, increasing ROM trend, and improved fine motor function and disability. KT improved spasticity, active movement, and muscle flexibility, resulting in more skilled and delicate hand function in chronic high-functioning stroke survivors.

NCT ID: NCT06183801 Completed - Metabolic Syndrome Clinical Trials

Effects of Probiotics on Metabolic Syndrome ,Intestinal Microflora and SCFA.

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

The improvement effects of GLAC biotech probiotics contains 5 specialized strains on the biochemical analysis and gut microbiota will be verified in the clinical trial through cooperation with the ADPRC. Through this project, the difference and improvement before and after the GLAC biotech probiotics taking will be clinically validated fromseveral aspects, including blood biochemical values, NGS gut microbiota analysis, GAIS and SCFAs levels. Therefore, by this industry- academic cooperation project, the investigators can explore the improvement of human gut microbiota by GLAC biotech probiotics, to understand the essence of clinical benefit, and the investigators expect the accomplishments of this project can help the consumers understand the added value and excellence of the GLAC products, and thus enhance consumer confidence and expand product markets.