跳至主要内容
临床试验/NCT04239495
NCT04239495Unknown不适用

Muscle Ageing Sarcopenia Study_Lifecourse (MASS_Lifecourse): Establishing a Life Course Cohort for Advances in the Prevention, Diagnosis and Treatment of Sarcopenia

Newcastle-upon-Tyne Hospitals NHS Trust1 个研究点 分布在 1 个国家目标入组 160 人开始时间: 2018年10月9日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
160
试验地点
1
主要终点
Sarcopenia phenotype- chair rise time

研究概览

简要总结

Sarcopenia is the loss of muscle mass and function with age. It has been recognised as an important health problem because it is common in older adults and associated with decline in physical function as well as a reduced quality of life. Sarcopenia can also lead to serious health consequences in terms of increased disability and the need for increased health and social care.

There is considerable interest in understanding what causes sarcopenia in order to develop new approaches to prevention, diagnosis and treatment. To gain a detailed understanding of sarcopenia across a range of ages, we have designed the Muscle Ageing Sarcopenia Study (MASS_Lifecourse) in collaboration with members of the public and patients.

详细描述

We aim to recruit 160 participants from Newcastle upon Tyne across an age range of 45-85 years from primary care, secondary care and the NIHR (National Institute for Health Research) Bioresource. Participants will receive a home visit from a researcher to complete a detailed health profile. Participants will then be invited to attend a clinical visit at Newcastle's Campus for Ageing and Vitality for imaging and muscle biopsy. A subsequent clinical visit will involve a fasting blood test, follow-up of the biopsy site and gather participants' views about taking part in the study.

The aims of the study:

  1. To determine if it is acceptable and feasible to recruit adults across a range of ages to undergo detailed studies of skeletal muscle including biopsy
  2. To understand how lifestyle is related to the characteristics of muscle
  3. To use advances in technology (an omics approach) to identify mechanisms of sarcopenia and biomarkers for early diagnosis
  4. To use findings from 2 and 3 to develop new approaches to treatment and also to invite participants to relevant trials
  5. To secure funding for maintaining and expanding the cohort

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Cross Sectional

入排标准

年龄范围
45 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Primary care source:
  • Registered patient with one of the GP (General Practice) surgeries identified as PIC (Participant Identification Centre) via North East and North Cumbria Clinical Research Network.
  • Secondary care source:
  • Attending a NuTH (Newcastle upon Tyne Hospitals NHS Foundation Trust) clinical area.
  • NIHR Bioresource:
  • Participants identified by the NIHR Bioresource Centre Newcastle as being eligible for the study and who have not previously expressed a wish to no longer be contacted about further studies.
  • For all recruitment sources:
  • Has capacity to consent.
  • Within the study age range (45-85 years).
  • Not taking any anticoagulant or antiplatelet medications (see below under exclusion criteria), with the exception of aspirin being taken for primary prevention (i.e. where there is no diagnosis of cardiovascular disease).

排除标准

  • Inability to give informed consent.
  • As the study involves biopsy of skeletal muscle, individuals who are taking medications that increase bleeding risk are excluded, specifically: i. anti-coagulant medication: warfarin, injected low-molecular weight heparins such as dalteparin, and direct oral anticoagulant drugs such as rivaroxaban and apixaban.
  • ii. anti-platelet medication such as clopidogrel or prasugrel. This also includes aspirin where an individual has a known history of cardiovascular disease. Aspirin being taken where there is no history of cardiovascular disease is acceptable, as we would consider there to be minimal risk of stopping the aspirin for 14 days prior to biopsies.
  • Individuals known to have diabetes mellitus, due to the increased risk of infection at the biopsy sites.
  • Individuals currently taking medication that suppresses the immune system (such as prednisolone or methotrexate), due to the increased risk of infection or poor healing of the biopsy sites.
  • Pregnancy, due to the exposure to small amount of ionising radiation during the DXA scan.
  • Individuals who use a wheelchair or who are unable to walk without assistance, as we would anticipate that the muscle biopsy procedure would not be feasible in these groups.
  • An individual who the NuTH clinician / GP feels it is inappropriate for the researchers to approach - the NuTH clinician / GP may consider an individual unsuitable for approach for reasons such as end stage terminal disease or safety risk.

结局指标

主要结局

Sarcopenia phenotype- chair rise time

时间窗: Baseline

Time to complete 5 chair rises (seconds)

Sarcopenia phenotype- walking speed

时间窗: Baseline

Usual walking speed (m/s)

Sarcopenia phenotype- grip strength

时间窗: Baseline

Maximum grip strength (Kg)

Sarcopenia phenotype- appendicular lean mass

时间窗: Baseline

Appendicular lean mass from DXA Scan (Kg)

次要结局

  • Cognitive and Psychosocial Function(Baseline)
  • Presence of Frailty(Baseline)
  • Geriatric Depression Scale(Baseline)
  • Patient-reported survey of patient health(Baseline)

研究者

发起方
Newcastle-upon-Tyne Hospitals NHS Trust
申办方类型
Other
责任方
Sponsor

研究点 (1)

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