Efficacy of Text-messaging on Activity Limitation in People With Chronic Low Back

NCT06903091 · tracked via the Priya Life Science France tracker

Sponsor

Assistance Publique - Hôpitaux de Paris

Phase

Not applicable

Started

2026-06-01

Last updated

2026-05-06

Condition(s) studied

Chronic Non-specific Low Back Pain

Investigational drug(s) / intervention(s)

SMS

SMS: Usual follow-up

Study summary

The main aim of this study was to evaluate the medium-term efficacy of an intervention involving personalized, automated text messaging (SMS), following face-to-face rehabilitation sessions, on activity limitation in people with chronic low back pain. We hypothesize that personalized SMS follow-up, following face-to-face rehabilitation sessions, could reduce activity limitation in people with chronic low back pain. Prospective multicenter randomized controlled trial.

Participants in both groups, experimental and comparator will have 4 face-to-face multidisciplinary rehabilitation sessions.

Participants in the 2 groups will have a face-to-face medical-kinesthetic clinical consultation at M3.

Participants in the experimental group will be monitored by personalized SMS messages over 6 months.

Eligibility

Sex

ALL

Min age

18 Years

Max age

70 Years

Healthy volunteers

Inclusion Criteria: * People with chronic low back pain (common low back pain, duration of low back pain \> 3 months) * People who own a cell phone and have mastered the basics of using it (consulting and sending sms). * Person with a moderate to high self-efficacy for exercise score (SEE score ≥ 31/90). * Patient having signed the study participation consent form. Patient affiliated to a social security scheme or entitled beneficiary Exclusion Criteria: * Any other pathology affecting postural stability or voluntary active mobility * Contraindication to exercise * Lumbar spine surgery in the 12 months prior to inclusion in the study * Inability to write, speak or read French * Psychiatric and/or behavioral disorders * Current pregnancy (declarative) No inclusion of persons covered by articles L. 1121-5 to L. 1121-8 and L. 1122-1-2 of the French Public Health Code (e.g. minors, protected adults, etc.).

Primary outcome measure(s)

Activity limitation — Month 6 (M6)
Change in score on the Roland Morris Disability questionnaire (RMDQ, 0 no activity limitation; 24, maximum limitation)

Trial sites (1)

Facility	City	Region	Status
Assistance Publique - Hôpitaux de Paris, Service de Rééducation et de Réadaptation de l'Appareil Locomoteur et des Pathologies du Rachis, Hôpital Cochin	Paris	Île-de-France Region

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06903091 on ClinicalTrials.gov ↗ ← All trials in France