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E-lombactifs: Evaluation of the Impact a Smartphone Application on Adherence an Exercise Program in Chronic Low Back Pain

E-lombactifs: Evaluation of the Impact a Smartphone Application on Adherence an Exercise Program in Chronic Low Back Pain

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04264949
Acronym
E-lombactifs
Enrollment
120
Registered
2020-02-11
Start date
2020-03-09
Completion date
2023-12-18
Last updated
2026-08-05

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

Conditions

Chronic Low Back Pain

Keywords

Chronic Low Back Pain, Physical activity, Adherence

Brief summary

The main objective is to assess the impact of smartphone application on adherence to a physical exercise program in chronic low back pain patients. Adherence to a physical exercise program will be assessed at the start of the protocol, at three weeks and six months. A control group will benefit from conventional care in a rehabilitation center and an intervention group will benefit from a conventional care in a rehabilitation center accompanied by education in the use of a smartphone application including physical exercises and information about low back pain. The hypothesis of the search is that adherence is better in intervention group than control group at 6 months due to education in the use of smartphone application.

Interventions

OTHEREducation in the use of smartphone app (Mon coach dos)

In addition to conventional care and the therapeutic education program, GA will benefit from three education sessions (one per week) on the use of the smartphone app mon coach dos

OTHERconventional care

conventional care and the therapeutic education program

Sponsors

University Hospital, Clermont-Ferrand
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

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

Inclusion criteria

* Adult People * With nonspecific chronic low back pain (according to the definition of the HAS) * Covered under the national health insurance * Giving informed written consent to participate in the study

Exclusion criteria

* Patient who do not meet the diagnostic criteria according to the definition of HAS * Behavioral disorders or comprehension difficulties making assessment impossible * Patient with a contraindication to physical exercise for medical reasons * Patient under guardianship, curatorship or safeguard of justice

Design outcomes

Primary

MeasureTime frameDescription
EARS : exercise adherence rating scaleday1EARS assess the adherence in physical activity program.

Secondary

MeasureTime frameDescription
OSWESTRY questionnaireday1, day 15, day 180Disability is measured by OSWESTRY
EPAP questionnaireday1, day 15, day 180The perceived barriers to and facilitators of physical activity are measured by EPAP
Pain measurment: numeric scaleday1, day 15, day 180The pain is measured by numeric scale
6 minutes' walk test (6MWT)day1, day 15, day 180Aerobic and functional capacities are measured by 6 minutes' walk test (6MWT)
aerobic capacitiesday1, day 15, day 180aerobic capacities are measured by sub maximal ergocycle test
muscular enduranceday1, day 15, day 180the muscular endurance of the erector muscles of the spine is measured by Sorensen test
muscular endurance of the flexor muscles of the spineday1, day 15, day 180the muscular endurance of the flexor muscles of the spine is measured by ITO test
muscular endurance of the extensor of the kneeday1, day 15, day 180the muscular endurance of the extensor of the knee is measured by Killy test
Core measurmentday1, day 15, day 180Core is measured by plank test
Flexibility on posterior chainday1, day 15, day 180Flexibility on posterior chain is measured by DDS test
Mobility on posterior chainday1, day 15, day 180Mobility on posterior chain is measured by Schober test

Countries

France

Contacts

PRINCIPAL_INVESTIGATORJean-Baptiste Lechauve

University Hospital, Clermont-Ferrand

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 6, 2026