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Sarcopenia clinical trials

View clinical trials related to Sarcopenia.

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NCT ID: NCT06468735 Completed - Sarcopenia Clinical Trials

The Relationship Among Sarcopenia, Preperitoneal Fat Thickness and Cholecystectomy

Start date: March 20, 2024
Phase: N/A
Study type: Interventional

The aim of this study was to examine the relationship between sarcopenia and visceral adiposity in participants with and without cholecystectomy. In this way, the long-term effects of cholecystectomy operations, which are commonly performed in the society and thought to be harmless, will be evaluated.

NCT ID: NCT06407583 Completed - Diabetes Clinical Trials

ProMIO2.0; A Powerful Lifestyle Intervention for Older Adults From Ethnic Minorities

ProMIO2
Start date: May 24, 2022
Phase: N/A
Study type: Interventional

Older adults from ethnic minorities show on average a worse disease risk profile compared to the majority populations. An important risk factor to develop chronic diseases is the loss of muscle mass and functioning, also known as sarcopenia. Several randomized controlled trials (RCTs) showed that the combination of adequate protein intake and physical exercise is most effective to prevent the loss of muscle mass, strength and functioning in older adults. However, until shortly, no intervention that included protein and exercise was available that accounted for the special socio-cultural needs of ethnic minority populations. Therefore the Amsterdam University of Applied Sciences (AUAS) and ProMIO project group developed a cultural sensitive lifestyle intervention with protein and exercise carried out by dieticians and physical therapists to provide a tailored treatment for older adults from ethnic minorities. This project aims to evaluate the effectiveness of this new intervention on protein intake, physical activity behavior, muscle mass, muscle strength, function and quality of life. The cost-effectiveness of this new intervention will also be evaluated.

NCT ID: NCT06354348 Completed - Sarcopenia Clinical Trials

Practical Ultrasonographic Detection of Sarcopenia in Patients With Long-term Gastrectomy

Start date: December 6, 2023
Phase: N/A
Study type: Interventional

The investigators aimed to evaluate long-term sarcopenia in patients with total and distal gastrectomy by measuring the anterior thigh muscle with USG, which is a more specific and easy method.

NCT ID: NCT06347965 Completed - Sarcopenia Clinical Trials

Construction and Effect Evaluation of the Low Load Blood Flow Restriction Training Program for Lung Cancer Patients Complicated With Sarcopenia During Chemotherapy

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

The goal of this clinical trial is to verify the effectiveness and safety of the low load blood flow restriction training program. The intervention effect, tolerance and compliance of low load blood flow restriction training and progressive resistance training on lung cancer patients complicated with sarcopenia during chemotherapy will be compared, in order to provide new ideas for improving or reversing sarcopenia. The main questions it aims to answer are: Can low load blood flow restriction training improve sarcopenia in chemotherapy induced lung cancer patients? Which training method is more effective and tolerable between low load blood flow restriction training and progressive resistance training? Participants will be randomly divided into 3 groups: 1. Routine care group (Control group, CON): The researchers will provide participants with regular exercise and dietary guidance. 2. Low load blood flow restriction group (LL-BFRT): The researchers will provide participants with a low load blood flow restriction training program constructed by our research group. 3. Progressive resistance training group (PRE): The researchers will provide participants with progressive resistance training.

NCT ID: NCT06314516 Completed - Esophageal Cancer Clinical Trials

Influence of Nutrition and Sarcopenia on Esophageal Cancer Outcomes

INSPECT
Start date: December 27, 2017
Phase:
Study type: Observational

Prospective multicenter longitudinal (observational) study recruiting from tertiary centers for the surgical management of esophageal cancer; Virginia Mason Medical Center (Seattle, USA) and St Mary's Hospital (Imperial College, London, UK). This is intended to be a pilot study.

NCT ID: NCT06277193 Completed - Sarcopenia Clinical Trials

Investigation of the Relationship Between Sarcopenia and Balance, Fear of Falling and Fall Risk in Older Female Patients

Start date: November 3, 2020
Phase:
Study type: Observational [Patient Registry]

This study (study type: cross-sectional) aims to investigate the relationship of sarcopenia level with balance, fear of falling and risk of falling in the elderly female population. In the first stage, 166 participants were divided into two groups: sarcopenia and non-sarcopenia. Afterwards, they were categorized according to sarcopenia level (probable sarcopenia group, sarcopenia group, severe sarcopenia group, group without sarcopenia) and comparisons were made between these subgroups. Then, they were evaluated with various scales and tests (in terms of balance, fear of falling and risk of falling).

NCT ID: NCT06261372 Completed - Clinical trials for Hemodialysis Patients With Sarcopenia

Mindfulness Meditation Combined With Progressive Muscle Relaxation Training for Uremic Sarcopenia

Start date: August 15, 2023
Phase: N/A
Study type: Interventional

To study the effect of mindfulness meditation combined with progressive muscle relaxation training on clinical efficacy and quality of life in maintenance hemodialysis (MHD) patients with sarcopenia. Eligible sarcopenic patients in our hospital were randomly assigned to a control group (n = 24) and an intervention group (n = 25). The control group received conventional dialysis treatment, while the intervention group received mindfulness meditation combined with progressive muscle relaxation training during the interdialysis period in addition to conventional dialysis treatment. The effect of the intervention was evaluated after 12 weeks.To observe whether the combined intervention training can improve the motor ability and quality of life of patients with sarcopenia in a short period of time.

NCT ID: NCT06254573 Completed - Hemiplegia Clinical Trials

The Relationship Of Ultrasonographic Measurements With Sarcopenia in Stroke

Start date: May 10, 2022
Phase:
Study type: Observational [Patient Registry]

introduction:The aim of this study was to show the relationship of distal femoral cartilage and quadriceps thicknesses with functional status and presence of sarcopenia in ambulatory stroke patients with voluntary movement. Materials and Method: Forty-eight patients who were diagnosed with stroke due to cerebrovascular disease, had started voluntary movement, and had a motor recovery of 3 or above according to Brunnstrom's Staging were included in this cross-sectional study.

NCT ID: NCT06248437 Completed - Sarcopenia Clinical Trials

Prototype of Innovative Food Product to Improve Respiratory and Peripheral Muscle Function in Humans

HIC1
Start date: March 30, 2019
Phase:
Study type: Observational

HIC1® compound has a presence in the form of a gel, which facilitates its oral intake (direct or diluted with water) and also administration through gastrostomy tubes or nasogastric tubes. All received a dose of 30 grams of gel.

NCT ID: NCT06238206 Completed - Stroke Clinical Trials

What User-requirements Need to be Considered When Developing a Lower-limb Exoskeleton? A Qualitative Study.

Start date: January 17, 2024
Phase: N/A
Study type: Interventional

The goal of this study is to identify the needs and requirements of end-users regarding the implementation of a lower-limb exoskeleton in a remote home setting. The end-users include older adults with sarcopenia, post-stroke individuals and physiotherapists. The main question it aims to answer is: • What are the needs and requirements of the end-user population when developing a lower-limb exoskeleton that can be implemented in a remote home setting? Participants will engage in three separate focus group sessions, in which they will discuss the predetermined topics. Interactions between the participants will be guided by open questions.