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Cardiorespiratory fitness testing for patients with degenerative lumbar spine disease

Clinical application and usefulness of practical cardiorespiratory fitness assessment in patients with degenerative lumbar spine disease: validity and reliability - Cardiorespiratory fitness testing for patients with degenerative lumbar spine disease

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON58376
Enrollment
55
Registered
2025-10-31
Start date
2026-01-01
Completion date
Unknown
Last updated
2026-03-16

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

Conditions

Degenerative lumbar spine disease Low back pain

Interventions

No intervention. Testing the validity of the SRT compared with the CPET as gold standard&nbsp

Sponsors

VieCuri Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Age =18 years;Degenerative disorder of the lumbar spine: degenerative disc disease, spondylosis, spondylolysis/-listhesis (grade 1 or 2), spinal stenosis, adjacent level disease, post-herniotomy, post-laminectomy instability (iatrogenic instability) or (recurrent) disc herniation;Adult patients with an indication for open lumbar spinal decompression (i.e. laminectomy),  lumbar discectomy or 1-3 level LSF (either open or percutaneous). LSF includes a Transforaminal Lumbar Interbody Fusion (TLIF) with decompression surgery;Conservative treatment of the lumbar spine (e.g. pain optimisation, physiotherapy)No contraindications for exercise testing (physical activity readiness questionnaire [PAR-Q]: see Appendix 1);Being proficient in the Dutch language.

Exclusion criteria

Exclusion criteria: Non-degenerative disorder of the spine: i.e. traumatic, oncological, infection;Indication for more than 3 level spinal fusion;Unable to ride the cycle ergometer (whatever the reason);Unwillingness to adhere to study protocol (no informed consent).

Design outcomes

Primary

MeasureTime frame
The main study parameters are the attained work rate at peak exercise (WRpeak, in W) at both SRTs, as well as the achieved VO2 at the VAT (mL/min) and VO2peak (mL/min) during CPET. Primary objective is to test the validity of the SRT as practical alternative performance-based test of cardiorespiratory fitness, to be examined by correlating test scores to CPET scores. 

Secondary

MeasureTime frame
Second, we aim to determine the test-retest reproducibility of the SRT in these patients by evaluating the reliability and agreement of test scores attained at two separate occasions. 

Countries

Netherlands

Contacts

Public ContactE.R.C. Janssen

VieCuri Medisch Centrum

estherjanssen@viecuri.nl077 320 5555

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Mar 20, 2026