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Home-based Cycling for People With Lumbar Spinal Stenosis (FLEXCAL)

Primary Purpose

Symptomatic Lumbar Spinal Stenosis

Status
Not yet recruiting
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
Home-based cycling program
usual care
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Symptomatic Lumbar Spinal Stenosis focused on measuring Lumbar spinal stenosis, Neurogenic claudication, Low back pain, Exercise therapy, Endurance training, Cycling, Randomized trial

Eligibility Criteria

50 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • age ≥ 50 year-old
  • radicular claudication (i.e. walking-induced low back, buttock and/or leg pain, relieved in siting and/or lumbar flexion positions) diagnosed by a physician
  • MRI or CT-scan findings consistent with LSS reported on a written radiology report provided by a board-certified radiologist or a resident in radiology

Exclusion Criteria:

  • inability to speak and/or read French language
  • inability or refusal to perform ergometric bicycle at home
  • patients already having an ergometric bicycle at home
  • history of lumbar spine surgery in the previous 12 months
  • cognitive disorders
  • severe neurologic or vascular disorders involving the lower limbs
  • contraindication to a rehabilitation program assessed by medical examination
  • people under tutorship or curatorship
  • protected adults

Sites / Locations

  • Assistance Publique - Hôpitaux de Paris, Service de Rééducation et de Réadaptation de l'Appareil Locomoteur et des Pathologies du Rachis, Hôpital Cochin

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Home-based cycling program associated to usual care

Outpatient physiotherapy

Arm Description

Outcomes

Primary Outcome Measures

Change in back-specific activity limitations
Mean change from baseline in mean back-specific activity limitations in the previous month using the self-administered Oswestry Disability Index (ODI) total score (0 no limitations and 100 maximal limitations).

Secondary Outcome Measures

Change in maximal walking distance
Mean change from baseline in mean maximal walking distance (meters) using an adapted version of the self-paced walking-test
Change in lumbar pain
Mean change from baseline in mean low back pain intensity in the previous 48 hrs on a self-administered 11-point pain numeric rating scale (0 no pain and 100 maximal pain)
Change in radicular pain
Mean change from baseline in mean radicular pain intensity in the previous 48 hrs on a self-administered 11-point pain numeric rating scale (0 no pain and 100 maximal pain)
Change in the physical component of health-related quality of life
Mean change from baseline in the mean physical component of health-related quality of life assessed by the physical component score of the self-administered 12-Item Short Form Survey (9.95 worst possible and 70.02 best possible)
Change in lumbar spinal stenosis-specific activity limitations
Mean change from baseline in mean LSS-specific activity limitations using the physical function subscore of the self-administered Zurich Claudication Questionnaire (1 no limitations and 4 maximal limitations)
Change in back-specific activity limitations
Mean change from baseline in mean spine-specific activity limitations assessed by the total score of the self-administered Oswestry Disability Index (0 no limitations and 100 maximal limitations)
Percentage of patients who undergo spinal surgery
Self-reported spinal surgery for lumbar spinal stenosis

Full Information

First Posted
August 29, 2019
Last Updated
September 26, 2022
Sponsor
Assistance Publique - Hôpitaux de Paris
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1. Study Identification

Unique Protocol Identification Number
NCT04075539
Brief Title
Home-based Cycling for People With Lumbar Spinal Stenosis
Acronym
FLEXCAL
Official Title
Home-based Cycling Using Connected Ergometric Bicycles for People With Lumbar Spinal Stenosis: a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
March 2023 (Anticipated)
Primary Completion Date
July 2023 (Anticipated)
Study Completion Date
March 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The main objective of the study is to compare the efficacy on back-specific activity limitations at 4 months after-randomisation of home-based cycling using connected ergometric bicycles associated with usual care to usual care.
Detailed Description
Lumbar spinal stenosis is a prevalent and disabling condition in elderly people. Lumbar spinal stenosis results in back and leg pain when standing and walking (radicular claudication), while symptoms regress in sitting position. The inability to stand or walk significantly impairs functioning and health-related quality of life of elders, and has an important healthcare cost. The 2 main treatment options for lumbar spinal stenosis are conservative or surgical treatments. Previous data suggested that laminectomy may be more effective on pain and function than conservative therapy. However, the benefit-risk balance of surgery should be carefully considered in this population with numerous co-morbidities, and evidence is inconsistent. Therefore, conservative therapy is usually the first line option. Data regarding exercise therapy are scarce. Flexion-based exercises are usually recommended. A pilot study suggested that flexion-based endurance training program, namely cycling, could be an effective and safe method to improve pain, function and health-related quality of life in elderly people with chronic lumbar pain. However, barriers to adhering to the program were detected and might have influenced clinical endpoints. Non-pharmacological interventions in spinal conditions are not 'one-size-fits-all' and measures to enhance adherence have to be applied. The hypothesis is that home-based cycling using connected ergometric bicycles associated with usual care could be more effective than usual care in reducing back-specific activity limitations at 4 months in people with lumbar spinal stenosis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Symptomatic Lumbar Spinal Stenosis
Keywords
Lumbar spinal stenosis, Neurogenic claudication, Low back pain, Exercise therapy, Endurance training, Cycling, Randomized trial

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Masking Description
single-blind
Allocation
Randomized
Enrollment
302 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Home-based cycling program associated to usual care
Arm Type
Experimental
Arm Title
Outpatient physiotherapy
Arm Type
Other
Intervention Type
Other
Intervention Name(s)
Home-based cycling program
Intervention Description
Usual care (i.e. standardized prescription of 6 sessions of outpatient physiotherapy), and 1 supervised session of cycling aimed at explaining how to use the connected ergometric bicycle and at designing a personalized home-based cycling program a 12-month home-based cycling program using connected ergometric bicycles which intensity and dose are self-determined 3 phone or email contacts with a care provider to deliver positive feedbacks and encouragements
Intervention Type
Other
Intervention Name(s)
usual care
Intervention Description
A prescription of 6 sessions of outpatient physiotherapy
Primary Outcome Measure Information:
Title
Change in back-specific activity limitations
Description
Mean change from baseline in mean back-specific activity limitations in the previous month using the self-administered Oswestry Disability Index (ODI) total score (0 no limitations and 100 maximal limitations).
Time Frame
4 months after-randomization
Secondary Outcome Measure Information:
Title
Change in maximal walking distance
Description
Mean change from baseline in mean maximal walking distance (meters) using an adapted version of the self-paced walking-test
Time Frame
4 months post-randomization
Title
Change in lumbar pain
Description
Mean change from baseline in mean low back pain intensity in the previous 48 hrs on a self-administered 11-point pain numeric rating scale (0 no pain and 100 maximal pain)
Time Frame
4, 6 and 12 months post-randomization
Title
Change in radicular pain
Description
Mean change from baseline in mean radicular pain intensity in the previous 48 hrs on a self-administered 11-point pain numeric rating scale (0 no pain and 100 maximal pain)
Time Frame
4, 6 and 12 months post-randomization
Title
Change in the physical component of health-related quality of life
Description
Mean change from baseline in the mean physical component of health-related quality of life assessed by the physical component score of the self-administered 12-Item Short Form Survey (9.95 worst possible and 70.02 best possible)
Time Frame
4, 6 and 12 months post-randomization
Title
Change in lumbar spinal stenosis-specific activity limitations
Description
Mean change from baseline in mean LSS-specific activity limitations using the physical function subscore of the self-administered Zurich Claudication Questionnaire (1 no limitations and 4 maximal limitations)
Time Frame
4, 6 and 12 months post-randomization
Title
Change in back-specific activity limitations
Description
Mean change from baseline in mean spine-specific activity limitations assessed by the total score of the self-administered Oswestry Disability Index (0 no limitations and 100 maximal limitations)
Time Frame
6 and 12 months post-randomization
Title
Percentage of patients who undergo spinal surgery
Description
Self-reported spinal surgery for lumbar spinal stenosis
Time Frame
From baseline to 12 months post-randomization

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age ≥ 50 year-old radicular claudication (i.e. walking-induced low back, buttock and/or leg pain, relieved in siting and/or lumbar flexion positions) diagnosed by a physician MRI or CT-scan findings consistent with LSS reported on a written radiology report provided by a board-certified radiologist or a resident in radiology Exclusion Criteria: inability to speak and/or read French language inability or refusal to perform ergometric bicycle at home patients already having an ergometric bicycle at home history of lumbar spine surgery in the previous 12 months cognitive disorders severe neurologic or vascular disorders involving the lower limbs contraindication to a rehabilitation program assessed by medical examination people under tutorship or curatorship protected adults
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Christelle Nguyen, MD, PhD
Phone
+33 1 58 41 25 35
Email
christelle.nguyen2@aphp.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Laetitia PEAUDECERF, PhD
Phone
+33 1 58 41 12 13
Email
laetitia.peaudecerf@aphp.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christelle Nguyen, MD, PhD
Organizational Affiliation
Université de Paris, Faculté de Médecine Paris Descartes
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
François Rannou, MD, PhD
Organizational Affiliation
Université de Paris, Faculté de Médecine Paris Descartes
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Isabelle Boutron, MD, PhD
Organizational Affiliation
Université de Paris, Faculté de Médecine Paris Descartes
Official's Role
Study Chair
Facility Information:
Facility Name
Assistance Publique - Hôpitaux de Paris, Service de Rééducation et de Réadaptation de l'Appareil Locomoteur et des Pathologies du Rachis, Hôpital Cochin
City
Paris
State/Province
Île-de-France
ZIP/Postal Code
75014
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Christelle Nguyen, MD, PhD
Phone
+33 1 58 41 29 45
Email
christelle.nguyen2@aphp.fr
First Name & Middle Initial & Last Name & Degree
François Rannou, MD, PhD
Phone
+33 1 58 41 25 35
Email
francois.rannou@aphp.fr

12. IPD Sharing Statement

Citations:
PubMed Identifier
31982599
Citation
Nguyen C, Boutron I, Roren A, Baron G, Pauwels C, Lefevre-Colau MM, Poiraudeau S, Dupeyron A, Coudeyre E, Rannou F. Home-based cycling using connected ergometric bicycles for people with lumbar spinal stenosis (FLEXCAL): Protocol for a randomised trial. Ann Phys Rehabil Med. 2021 Mar;64(2):101351. doi: 10.1016/j.rehab.2019.12.006. Epub 2020 Jan 23. No abstract available.
Results Reference
background

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Home-based Cycling for People With Lumbar Spinal Stenosis

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