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Effect of an Interdisciplinary Spine Rehabilitation Program

PROGRESS: The Effect of an Interdisciplinary Program for Rehabilitation for Spinal Disorders

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06030570
Acronym
PROGRESS
Enrollment
90
Registered
2023-09-11
Start date
2023-08-22
Completion date
2025-12-31
Last updated
2025-09-23

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

Conditions

Low Back Pain, Spine Disease

Brief summary

The goal of this research project is to evaluate the effectiveness of the current interdisciplinary rehabilitation program (Revita) and follow-up trajectory for chronic lumbar spine disorders in the University Hospitals Leuven.

Interventions

OTHERRehabilitation program (Revita)

Multidisciplinary programs in an outpatient hospital setting are coordinated by specialists in Physical and Rehabilitation Medicine. These programs combine a physical part (e.g., specific exercises, manual techniques) with at least one other element (psychological, social, educational or occupational intervention). In a multidisciplinary spine rehabilitation program, a maximum of 36 sessions over a maximum time period of 6 months is offered. Afterwards, a (monodisciplinary) follow-up trajectory (K15) is possible, consisting of maximum 104 sessions a year.

Sponsors

KU Leuven
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults, age \> 18 years * Spine problem for \> 6 weeks, needing interdisciplinary care (risk factors, failure of first line treatment, etc) * Inclusion in Revita program * Informed consent to participate

Exclusion criteria

* Patients without sufficient understanding of the Dutch language * Unable to participate in 2h rehabilitation sessions with exercises

Design outcomes

Primary

MeasureTime frameDescription
Change in Oswestry Disability Index (ODI)baseline - 6 months - 1 yearChange in functional impairment (before vs. after rehabilitation program) minimum score: 0 maximum score: 100 a higher score corresponds with more functional impairment
Change in painbaseline - 6 months - 1 yearChange in numeric rating scale (NRS) for low back/leg pain (before vs. after rehabilitation program) minimum score: 0 maximum score: 10 a higher score corresponds with more pain

Secondary

MeasureTime frameDescription
Effect on anxiety and depressionbaseline - 6 months - 1 yearChange in Hospital Anxiety and Depression Scale (HADS) (before vs. after rehabilitation program) minimum score: 0 maximum score: 21 (anxiety) - 21 (depression) a higher score corresponds with a higher suspicion for anxiety/depression
Effect on kinesiophobiabaseline - 6 months - 1 yearChange in Tampa scale for Kinesiophobia (TSK) score (before vs. after rehabilitation program) minimum score: 17 maximum score: 68 a higher score corresponds with an increasing degree of kinesiophobia
Effect on fear-avoidance beliefsbaseline - 6 months - 1 yearChange in Fear Avoidance Beliefs Questionnaire (FABQ) score (before vs. after rehabilitation program) minimum score: 0 maximum score: 96 a higher score corresponds with stronger fear avoidance beliefs
Effect on body awarenessbaseline - 6 months - 1 yearChange in Fremantle Back Awareness Scale Questionnaire score (before vs. after rehabilitation program) minimum score: 0 maximum score: 36 a higher score corresponds with a worse back-specific body perception
Effect on quality of lifebaseline - 6 months - 1 yearChange in EuroQoL 5D (before vs. after rehabilitation program) 5 items with 3 levels Scale to assess health: 0-100 a higher score corresponds with better health
Return to Work self-efficacybaseline - 6 months - 1 yearthe Return to Work Self-Efficacy questionnaire minimum score: 1 maximum score: 6 a higher score corresponds with a higher level of self-efficacy
Return to workbaseline - 6 months - 1 yearnumber of days to return to work
Effect on functioningbaseline - 6 months - 1 yearChange in Patient Specific Functional scale (PSFS) minimum score: 0 maximum score: 10 a higher score corresponds with a better functional level
Effect on medication usebaseline - 6 months - 1 yearChange in Medication Quantification Scale (MQS) a higher score corresponds with a higher medication use
Treatment experience6 months - 1 yearPatient Global impression of change (PGIC) minimum score: 1 maximum score: 7 a higher score corresponds with less impression of change
Effect on risk stratification toolbaseline - 6 months - 1 yearChange in Örebro score (before vs. after rehabilitation program) minimum score: 0 maximum score: 100 a higher score corresponds with a higher risk profile

Countries

Belgium

Contacts

Primary ContactSofie Rummens, MD
sofie.rummens@uzleuven.be003216338700

Outcome results

None listed

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