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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06448871
Other study ID # TCRD-TPE-112-28
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date October 17, 2022
Est. completion date June 30, 2024

Study information

Verified date May 2024
Source Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation
Contact Valeria Chiu, MD
Phone 0982766578
Email haydenbell28@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of the study is to examine the clinical applicability of ultrasound as a diagnostic tool for sarcopenia in individuals with PWS by investigating the association between ultrasound-derived measurements, DXA-derived measurements, and sarcopenia-related outcomes.


Description:

Sarcopenia is an age-related loss of muscle mass plus low muscle strength, and/or low physical performance, that may affect over 25% of individuals over the age of 60, resulting in an increased likelihood of developing disability. Abnormal body composition with an increased in body fat mass and a decreased in skeletal muscle mass were noted in individuals with Prader Willi syndrome (PWS), thought to be related to hormonal deficiencies due to hypothalamic dysfunction, presenting as a unique congenital model of sarcopenia. Muscle mass can be measured by dual-energy X-ray absorptiometry (DXA) scan device, but it is expensive, increased radiation exposure, and not easily accessible in all clinical practice. Ultrasound (USD) is a non-invasive, without ionising radiation, low-cost, and easily accessible tool for the assessment of soft tissue. There were increasing evidence for the use of USD in the measurement of muscle thickness (MT), cross-sectional area (CSA) and pennate anle (PA) of different muscle groups in different populations. However, the use of USD as a routine diagnostic tool in individuals with PWS has not been reported yet. The aim of the study is to examine the clinical applicability of ultrasound as a diagnostic tool for sarcopenia in individuals with PWS by investigating the association between ultrasound-derived measurements, DXA-derived measurements, and sarcopenia-related outcomes.


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date June 30, 2024
Est. primary completion date June 30, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 7 Years to 65 Years
Eligibility Inclusion Criteria: - Genetically diagnosed individuals with PWS who can cooperate with the examinations AND - Age-matched control individuals with normal BMI. Exclusion Criteria: - Individuals with PWS or age-matched control individuals with arthritis, fracture, or severe musculoskeletal deformities that would interfere with the examinations. - Individuals with severe cognitive impairment who cannot read or sign the written consent.

Study Design


Intervention

Diagnostic Test:
Ultrasound assessment of the right lower extremity muscles
Rectus femoris cross sectional area (RFCSA), RF muscle thickness, vastus lateralis (VL) muscle thickness, Gastrocnemius medialis (GM) muscle thickness, VL pennation angle (PA), and GM PA.
Dual-energy X-ray absorptiometry (DXA) scan
skeletal muscle mass (SM), appendicular skeletal muscle mass index (ASMI), total lean body mass (LBM), total fat mass (BF), percentage fat mass, and fat mass index (FMI).

Locations

Country Name City State
Taiwan Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation New Taipei City

Sponsors (1)

Lead Sponsor Collaborator
Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Muscle thickness ultrasound Ultrasound scanning of the muscle thickness of rectus femoris (RF), vastus lateralis (VL), and gastrocnemius medialis (GM) using B-mode ultrasonography (LOGIQ S8, GE Healthcare, USA) and a 7-15 MHz linear array transducer. 1 day
Primary Cross-sectional area ultrasound Ultrasound scanning of the cross sectional area of rectus femoris (RF) using B-mode ultrasonography (LOGIQ S8, GE Healthcare, USA) and a 7-15 MHz linear array transducer. 1 day
Primary Pennation angle ultrasound Ultrasound scanning of the pennation angles of vastus lateralis (VL) and gastrocnemius medialis (GM) using B-mode ultrasonography (LOGIQ S8, GE Healthcare, USA) and a 7-15 MHz linear array transducer. 1 day
Primary DXA: total lean body mass Lean index of total lean body mass (LBM) with Hologic QDR-4500A, Hologic, Inc., Waltham, MA, USA 1 day
Primary DXA: skeletal muscle (SM) Lean index of skeletal muscle (SM) with Hologic QDR-4500A, Hologic, Inc., Waltham, MA, USA 1 day
Primary DXA: appendicular skeletal muscle mass index (ASMI) Lean index of appendicular skeletal muscle mass index (ASMI) with Hologic QDR-4500A, Hologic, Inc., Waltham, MA, USA 1 day
Primary DXA: fat mass index (FMI) Adipose index of fat mass index using Hologic QDR-4500A, Hologic, Inc., Waltham, MA, USA. 1 day
Primary DXA: body fat mass (BFM) Adipose index of body fat mass (BFM) using Hologic QDR-4500A, Hologic, Inc., Waltham, MA, USA. 1 day
Primary DXA: percentage fat mass Adipose index of percentage fat mass using Hologic QDR-4500A, Hologic, Inc., Waltham, MA, USA. 1 day
Secondary Handgrip and lateral pinch strength Grip strength and lateral pinch will be assessed bilaterally using an isometric Baseline hydraulic hand dynamometer and pinch gauge. 1 day
Secondary Physical performance test: SPPB The short physical performance battery (SPPB) will be used, which measures balance, walking speed, strength, and endurance in the lower limbs, and is scored from zero to 12 (worst to best score). 1 day
Secondary Physical performance test: gait speed In the gait speed test participants walk over a 4-meter distance at their normal pace. 1 day
Secondary Physical performance test: five-time chair stand test In the 5-time chair stand test participants perform five sit-to-stand movements as quickly as possible 1 day
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