NCT06312774

Brief Summary

Sarcopenia, the loss of muscle mass and strength with ageing, is a prevalent condition in older adults, particularly those with chronic lung diseases like COPD and interstitial lung disease. The condition exacerbates the decline in physical ability, leading to decreased mobility, impaired quality of life, and increased disability. Sarcopenia's prevalence varies across populations, estimated to affect up to 10% of adults over 60 worldwide, with higher rates reported in studies employing consensus definitions of sarcopenia. The prevalence is even higher in patients with chronic lung diseases, reaching up to 26.6%. Sarcopenia's impact on health-related quality of life has been widely investigated. The condition is associated with various comorbidities, including chronic heart failure, obesity, diabetes, and chronic kidney disease, all negatively impacting the quality of life. The proposed study's primary aim is to assess the feasibility of the FACS (finding, assessing, confirming, severity) approach in determining sarcopenia's prevalence in the chronic lung disease population. FACS includes screening, strength measurements, and bioelectrical impedance analysis (BIA) to confirm sarcopenia. The study will also explore potential mechanisms associated with sarcopenia in this population, using proteome and single-cell transcriptome profiles. These multi-omics approaches provide a comprehensive view of the cellular and molecular changes underlying sarcopenia.In particular, the study will evaluate patient acceptance, time efficiency of each test, and recruitment effectiveness. The outcomes will guide the design and execution of subsequent, larger studies and provide preliminary data for power calculation for the full-scale study.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
49

participants targeted

Target at P25-P50 for all trials

Timeline
8mo left

Started Apr 2024

Typical duration for all trials

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress76%
Apr 2024Jan 2027

First Submitted

Initial submission to the registry

March 8, 2024

Completed
7 days until next milestone

First Posted

Study publicly available on registry

March 15, 2024

Completed
1 month until next milestone

Study Start

First participant enrolled

April 18, 2024

Completed
1.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 7, 2025

Completed
1.2 years until next milestone

Study Completion

Last participant's last visit for all outcomes

January 4, 2027

Expected
Last Updated

March 15, 2024

Status Verified

March 1, 2024

Enrollment Period

1.6 years

First QC Date

March 8, 2024

Last Update Submit

March 14, 2024

Conditions

Outcome Measures

Primary Outcomes (1)

  • Sarcopenia

    feasibility of using the FACS approach and molecular analyses to investigate the association between sarcopenia and chronic lung disease

    3 years

Study Arms (2)

Individuals with Chronic Lung Disease

Other: This is observational study

Healthy Controls

Other: This is observational study

Interventions

This is observational study

Healthy ControlsIndividuals with Chronic Lung Disease

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Sarcopenia, the condition of losing muscle mass and strength as we age, is especially common in older adults who also have chronic lung diseases such as COPD (a type of obstructive lung disease that makes it hard to breathe) and interstitial lung disease (a type of lung disease that affects the tissue and space around the air sacs of the lungs).

You may qualify if:

  • Adult patients diagnosed with chronic lung disease (≥ 18years).
  • Only patients who are willing and able to provide informed consent to participate in the study.

You may not qualify if:

  • Patients with other major comorbidities that could significantly impact muscle mass and function, such as severe heart failure, advanced liver or kidney disease, uncontrolled diabetes, or malignancies.
  • Patients with acute exacerbations of their chronic lung disease or any other acute illness at the time of the study. 3. Patients with a history of neuromuscular disorders or disability that could significantly affect muscle mass and function.
  • \. Patients who have undergone recent surgery in the past 6 months or have received specific treatments that could influence muscle mass and function, such as long-term corticosteroid use, chemotherapy, or radiation therapy.
  • \. Patients with life expectancy of less than 6 months 6. Patients who are unable or unwilling to comply with the study protocol or procedures.
  • \. Patients that are unable to give informed consent.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Sarcopenia

Condition Hierarchy (Ancestors)

Muscular AtrophyNeuromuscular ManifestationsNeurologic ManifestationsNervous System DiseasesAtrophyPathological Conditions, AnatomicalPathological Conditions, Signs and SymptomsSigns and Symptoms

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 8, 2024

First Posted

March 15, 2024

Study Start

April 18, 2024

Primary Completion

November 7, 2025

Study Completion (Estimated)

January 4, 2027

Last Updated

March 15, 2024

Record last verified: 2024-03