Bioindicators Associated With Sarcopenia Before and After Intensive Lifestyle Intervention

Sponsor
Lijun Yang (Other)
Overall Status
Completed
CT.gov ID
NCT06128577
Collaborator
Suzhou Municipal Hospital (Other)
99
1
2
5.1
19.6

Study Details

Study Description

Brief Summary

The goal of this clinical trial is to explore whether the bioindicators of body composition, nutrition-related indicators (lymphocytes, albumin), lipids, and thyroid hormones are associated with sarcopenia and the changes in these indicators after an intensive lifestyle intervention. The main questions it aims to answer are:

  • whether the bioindicators such as lymphocytes, albumin, lipids, thyroid hormones, fat mass, fat-free mass, and basal metabolic mass are associated with the development of sarcopenia.

  • the changes of these bioindicators that occur in older adults after going through an intensive intervention.

Participants will receive a 3-month intensive intervention consisting of an intensive nutritional intervention and an individually designed exercise intervention. Nutritional and exercise prescriptions are co-designed through a nutritionist and rehabilitation physician.

Researchers will compare bioindicators in the sarcopenia group before and after intensive lifestyle intervention to determine the association with sarcopenia.

Condition or Disease Intervention/Treatment Phase
  • Combination Product: 3-month intensive intervention
Phase 4

Study Design

Study Type:
Interventional
Actual Enrollment :
99 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Bioindicators Associated With Sarcopenia Before and After Intensive Lifestyle Intervention
Actual Study Start Date :
Mar 1, 2022
Actual Primary Completion Date :
Jul 31, 2022
Actual Study Completion Date :
Aug 2, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Sarcopenia group

After completing screening, 30 subjects in the sarcopenia group received a 3-month intensive intervention consisting of an intensive nutritional intervention and an individually designed exercise intervention. Nutritional and exercise prescriptions were co-designed through a nutritionist and rehabilitation physician.

Combination Product: 3-month intensive intervention
Intensive nutritional interventions were as follows: i)Estimation of ideal body weight according to height, calculation of calories by giving 30-40kcal/kg/day according to BMI stratification, and calculation of daily protein requirement at 1.5g/kg/day, which was finally converted into daily dietary recommendations according to the results of the calculations. ii)Distribution of additional protein supplementation by whey protein, each sachet containing 15g of whey protein. The resistance training program included 5 min of warm-up, 20 min of muscle strength training, and 5 min of slow walking and was performed three times a week. Resistance training involved a dumbbell and sandbags as weights for the major muscles of the upper and lower limbs. In the study, aerobic training is brisk walking or jogging for 30 minutes/day, five times a week.
Other Names:
  • Sarcopenia group
  • No Intervention: Normal control group

    Outcome Measures

    Primary Outcome Measures

    1. AMMI(appendicular muscle mass index) [baseline and 3 month]

      Bioelectrical impedance analysis was used to obtain appendicular muscle mass (AMM) and height. The unit of AMM and height were represented as kilogram and meter respectively. AMMI were calculated as AMM/height^2 (kg/m^2).

    Secondary Outcome Measures

    1. Fat mass [baseline and 3 month]

      Bioelectrical impedance analysis was used to obtain fat mass. The unit of fat mass was represented as kilogram.

    2. Fat-free mass [baseline and 3 month]

      Bioelectrical impedance analysis was used to obtain fat-free mass. The unit of fat-free mass was represented as kilogram.

    3. Basal metabolic mass [baseline and 3 month]

      Bioelectrical impedance analysis was used to obtain basal metabolic mass. The unit of basal metabolic mass was represented as kilocalorie.

    4. Lymphocyte count [baseline and 3 month]

      Lymphocyte counts were detected using a fully automated hematology analyzer (Mindray BC-6800, Shenzhen, China). The unit of lymphocyte count was represented as 10^9/L.

    5. Albumin [baseline and 3 month]

      Albumin was detected using a fully automated biochemistry analyzer (Hitachi 7600, Hitachi, Ltd., Tokyo, Japan). The unit of albumin was represented as g/L.

    6. Five items of blood lipid (triglycerides (TG), total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), very low-density lipoprotein cholesterol (VLDL-C)) [baseline and 3 month]

      Five items of blood lipid were detected using a fully automated biochemistry analyzer (Hitachi 7600, Hitachi, Ltd., Tokyo, Japan). The units of the five items of blood lipid were all represented as mmol/L.

    7. Thyroid hormones (thyroid stimulating hormone (TSH), free thyroxine (FT4), and free triiodothyronine (FT3)) [baseline and 3 month]

      Thyroid hormones were measured by chemiluminescence immunoassay (Abbott I2000, Abbott, Chicago, USA). The units of FT4 and FT3 were represented as pmol/L. The unit of TSH was represented as μIU/mL.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    65 Years to 90 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
      1. Resident elderly aged 65-90 years old in the district.
      1. Voluntary participation in the trial and signing the informed consent form.
    Exclusion Criteria:
      1. People with systemic severe diseases, organ failure, malignant tumors, neuromuscular degenerative diseases, or active weight loss.
      1. People with cognitive impairment, incapacitation, or severe mental illnesses who cannot cooperate with the test.
      1. People with cardiac pacemakers and artificial joint implantation or others who cannot undergo the BIA test.
      1. People with severe cardiorespiratory dysfunction and physical disabilities who cannot complete the exercise training.
      1. Incomplete data, refusal to participate in the survey, body composition analysis, and blood collection.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Suzhou Municipal Hospital Suzhou Jiangsu China 215000

    Sponsors and Collaborators

    • Lijun Yang
    • Suzhou Municipal Hospital

    Investigators

    • Study Director: Lijun j Yang, Master, Suzhou Municipal Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Lijun Yang, Physician in Charge, Suzhou Municipal Hospital
    ClinicalTrials.gov Identifier:
    NCT06128577
    Other Study ID Numbers:
    • LCZX201911
    First Posted:
    Nov 13, 2023
    Last Update Posted:
    Nov 13, 2023
    Last Verified:
    Nov 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Lijun Yang, Physician in Charge, Suzhou Municipal Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 13, 2023