The Five-repetition Sit-to-stand Test for Lower Back Pain or Radiculopathy

The Five-repetition Sit-to-stand Test as an Objective Measure of Functional Impairment in Patients With Lower Back Pain or Radiculopathy

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT03303300

Acronym

5R-STS

Enrollment

237

Registered

2017-10-06

Start date

2017-10-01

Completion date

2017-12-03

Last updated

2017-12-05

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

Conditions

Degenerative Disc Disease, Degenerative Spondylolisthesis, Herniated Disc, Nerve Root Compress;Lumbosac, Stenosis, Spinal

Brief summary

The five-repetition sit-to-stand test (5R-STS) has been used in many medical disciplines, but has never been correlated with or validated in regard to degenerative spinal diseases. The investigators aim to assess the possibility of using the standardized 5R-STS as an objective measure of functional impairment and pain severity in patients with degenerative lumbar spinal diseases.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Healthy volunteers

Yes

Inclusion criteria

This study will include 100 Patients: Inclusion Criteria: * Degenerative diseases of the lumbar spine (Herniated disc, lumbar stenosis, spondylolisthesis, degenerative disc disease) * Symptoms of lower back pain, neurogenic claudication, or radiculopathy

Exclusion criteria

* Hip or Knee prosthetics * Walking aides This study will also include 25 healthy volunteers: Inclusion Criteria: \- No degenerative spinal or lower extremity complaints

Design outcomes

Primary

Measure	Time frame	Description
5R-STS	0 weeks	The result of the standardized 5R-STS in seconds. If the patient is unable to complete the test, the results is noted as not possible.

Secondary

Measure	Time frame	Description
VAS back pain	0 weeks	Validated questionnaire (VAS BP) will be used to correlate the 5R-STS results with validated measures of functional impairment and pain severity.
VAS leg pain	0 weeks	Validated questionnaire (VAS LP) will be used to correlate the 5R-STS results with validated measures of functional impairment and pain severity.
EQ-5D-3L	0 weeks	Validated questionnaire (EQ-5D-3L) will be used to correlate the 5R-STS results with validated measures of functional impairment and pain severity.
Oswestry Disability Index	0 weeks	Validated questionnaire (ODI) will be used to correlate the 5R-STS results with validated measures of functional impairment and pain severity.
Roland-Morris-Disability Questionnaire	0 weeks	Validated questionnaire (RMDBQ) will be used to correlate the 5R-STS results with validated measures of functional impairment and pain severity.

Countries

Netherlands

Outcome results