Skip to content

A multicenter spinal sarcopenia cohort construction and the related diagnostic reference threshold establishment

A multicenter spinal sarcopenia cohort construction and the related diagnostic reference threshold establishment

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400084677
Enrollment
Unknown
Registered
2024-05-22
Start date
2024-06-01
Completion date
Unknown
Last updated
2024-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

spine-specific sarcopenia

Interventions

Multicenter Spine-Specific Sarcopenia Cohort:This study constitutes a long-term follow-up cohort of elderly individuals undergoing physical examinations, obtaining clinical information, muscle functio
Xinjiekou Community Cohort:This cohort study has completed the baseline data collection, and will continue to complete the follow-up in the second year after enrollment. This project uses both baselin

Sponsors

Laboratory of Bone Tissue Engineering of Beijing Research Institute of Traumatology and Orthopaedics
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: Multicenter Spine-Specific Sarcopenia Cohort: 1)Age 60 or above; 2)Gender unrestricted; 3)Informed consent; 4)Autonomous capacity; 5)Willing to cooperate with multiple follow-ups to reduce loss to follow-up. Xinjiekou Community Cohort: 1) Have certain activity ability and autonomous consciousness, and can cooperate to complete the full set of examinations; 2) voluntarily participate and sign the informed consent form.

Exclusion criteria

Exclusion criteria: Multicenter Spine-Specific Sarcopenia Cohort: 1)Patients with a history of spinal surgery; 2)Patients known to have congenital spinal deformities; 3)Patients known to have neuromuscular diseases; 4)Patients known to have rheumatic immune diseases (including ankylosing spondylitis); 5)Patients with spinal tumors, infections, or fractures; 6)Lumbar spondylolisthesis > II°, Cobb angle of scoliosis > 30°; 7)Patients with obvious spinal cord compression symptoms; 8)Patients with severe systemic diseases; 9)Patients with cognitive or communication impairments. Xinjiekou Community Cohort: 1) suffering from a serious or life-threatening illness; 2) refused to row CT examination; 3) unable to cooperate with the questionnaire survey; 4) Refusal to sign informed consent.

Design outcomes

Secondary

MeasureTime frame
Basic information;Physical examination of sensation and movement of lower limbs;Spinal muscle function test;Low dose chest CT (LDCT) scan;Daily activity, falls, and nutrition information;Muscle strength and physical function were tested;The living status and fall incidence during the follow-up period were analyzed;Low dose chest CT (LDCT) scan;Muscle strength and physical function indexes;

Primary

MeasureTime frame
Major fracture occurrences;

Countries

China

Contacts

Public ContactYajun Liu

Laboratory of Bone Tissue Engineering of Beijing Research Institute of Traumatology and Orthopaedics

drliuyajun@163.com+86 139 1187 8647

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026