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Physical Activity, Disability and Quality of Life Before and After Lumbar Spine Surgery

Accelerometry-based Physical Activity, Disability and Quality of Life Before and After Lumbar Spine Surgery: a Prospective Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03452449
Acronym
PA-LSS
Enrollment
29
Registered
2018-03-02
Start date
2017-06-01
Completion date
2019-06-30
Last updated
2019-09-18

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

Conditions

Disability Physical, Lumbar Spine Degeneration, Pain, Physical Activity, Quality of Life

Keywords

activity monitor, questionnaire, Oswestry Disability Index

Brief summary

To date it is unknown how physical activity levels in adults is limited before and after lumbar spine surgery and if physical activity level is associated with disability and limitations of quality of life. The main objective is to compare physical activity preoperatively and 6 and 12 weeks postoperatively in patients undergoing lumbar spine surgery with norm data. In addition, the investigators will study the association of changes in physical activity, disability and quality of live.

Detailed description

Patients scheduled for planned lumbar spine surgery will be contacted to participate in this study. All outcomes will be assessed within 1 week preoperatively and at 6 and 12 weeks postoperatively. Changes in outcome scores will be detected using analysis of variance. Association of changes in physical activity and changes in secondary outcomes will be detected using stepwise linear regression models.

Interventions

PROCEDUREplanned lumbar spine surgery

planned lumbar spine surgery including decompression, discectomy, foraminotomy, laminectomy

Sponsors

University Hospital, Basel, Switzerland
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years

Inclusion criteria

* primary lumbar spine surgery * single or multi level surgery on segments L2 to S1 (e.g. discectomy, decompression, laminectomy, foraminotomy) * German speaking

Exclusion criteria

* stabilisation or fusion surgery or surgery above L2 * previous lumbar spine surgery * indication: scoliosis, fracture, trauma, infection, tumor * limited walking ability due to other conditions * psychiatric conditions or dementia

Design outcomes

Primary

MeasureTime frameDescription
Physical activityup to 12 weeksmeasured using ActiGraph (accelerometer based activity monitor) as step counts, physical activity intensity during 7-day data capture period

Secondary

MeasureTime frameDescription
Disabilityup to 12 weeksmeasured using Oswestry Disability Index (questionnaire) (best score: 0 - no disability, worst score: 100)
Quality of life assessed by questionnaireup to 12 weeksmeasured using Short Form (SF)-36 (questionnaire) (worst score: 0; best score: 100 - highest quality of life)
Pain assessed by questionnaireup to 12 weeksmeasured using 10 cm visual analogue scale (VAS) lower back, legs (best score: 0 - no pain; worst score: 100)

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026