Delphi Study on Rehabilitation Following Lumbar Arthrodesis
Sponsor
Hasselt University (Other)
Overall Status
Unknown status
CT.gov ID
NCT03427294
Collaborator
Universitaire Ziekenhuizen Leuven (Other), KU Leuven (Other)
30
1
23.9
1.3
Study Details
Study Description
Brief Summary
Delphi study on perioperative rehabilitation after single level lumbar arthrodesis.
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
|
Detailed Description
The investigators aim to engage all care providers in UZ Leuven who are at some point involved in the rehabilitation path related to single level lumbar arthrodesis.
Study Design
Study Type:
Observational [Patient Registry]
Anticipated Enrollment
:
30 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Delphi Study on Rehabilitation Following Lumbar Arthrodesis in UZ Leuven (Belgium)
Actual Study Start Date
:
Jan 3, 2018
Anticipated Primary Completion Date
:
Dec 31, 2018
Anticipated Study Completion Date
:
Dec 31, 2019
Arms and Interventions
Arm | Intervention/Treatment |
---|---|
Care providers involved in lumbar arthrodesis surgeons, physiotherapists, behavioral therapists, researchers, occupational therapists |
Other: Delphi study
Delphi study on the optimal rehabilitation pathway following lumbar arthrodesis
|
Outcome Measures
Primary Outcome Measures
- Duration of perioperative rehabilitation following lumbar arthrodesis [January - December 2018]
duration defined in amount of weeks
- Physiotherapeutic content following lumbar arthrodesis [January - December 2018]
describing the physiotherapeutic modalities defined as manual therapy, exercise therapy, or cognitive behavioural therapy
- Frequency of physiotherapeutic intervention following lumbar arthrodesis [January - December 2018]
frequency defined as amount of physiotherapeutic visits per week
- Multidisciplinary character of perioperative rehabilitation following lumbar arthrodesis [January - December 2018]
amount and type of involved health care providers, as well as the interaction between
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
- The investigators aim to engage all care providers in UZ Leuven (Belgium) who are involved in the care of patients following lumbar arthrodesis.
Exclusion Criteria:
- N/A
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | UZ/KU Leuven | Leuven | Vlaams Brabant | Belgium | 3000 |
Sponsors and Collaborators
- Hasselt University
- Universitaire Ziekenhuizen Leuven
- KU Leuven
Investigators
- Principal Investigator: Lotte Janssens, PhD, PT, Hasselt University
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Lotte Janssens,
Prof. dr. Lotte Janssens,
Hasselt University
ClinicalTrials.gov Identifier:
NCT03427294
Other Study ID Numbers:
- KU/UZ Leuven S60109 - 2
First Posted:
Feb 9, 2018
Last Update Posted:
Feb 9, 2018
Last Verified:
Feb 1, 2018
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No