Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT06938568

Personalized Physical Back Training Program to Improve Physical Functioning in People With Non-specific Low Back Pain

Led by Claudio Perret · Updated on 2025-05-04

180

Participants Needed

1

Research Sites

134 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Personalized medicine and individualized therapeutic approaches are prominent in current research. But are these approaches also effective for treating non-specific low back pain (NSLBP)? NSLBP is one of the most common musculoskeletal issues, which can impair physical well-being, reduce the quality of life, and limit physical functioning. Additionally, it contributes to substantial direct and indirect healthcare costs, such as frequent doctor visits and work absences. Despite NSLBP being a significant burden for both individuals and society, effective alleviation methods remain unclear. The investigators' research project therefore aims to investigate whether personalized therapy, specifically a personalized physical back training program, can effectively address NSLBP. Within the context of NSLBP, the investigators' specific aim is to improve physical functioning as this outcome is considered relevant from all perspectives, including those of patients, clinical professionals, researchers, and guidelines.

CONDITIONS

Official Title

Personalized Physical Back Training Program to Improve Physical Functioning in People With Non-specific Low Back Pain

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Access to the University Sports of the Lucerne Universities (students, employees, alumni, or subscribers)
  • Non-specific low back pain lasting at least 6 weeks
  • Activity-limiting low back pain with at least one activity scored 50/100 or less on the PSFS scale
  • Age between 18 and 65 years
  • Ability to understand German language
  • Willingness to participate in the study
  • Written informed consent provided
Not Eligible

You will not qualify if you...

  • Specific low back pain
  • Red flags indicating serious pathology or specific low back pain
  • On waiting list for or less than 12 months after lower back surgery
  • Pregnant or gave birth within the last 12 months
  • Diagnosed central neurological disease
  • Not allowed to exercise
  • Participation in the feasibility study
  • Expecting to be absent for more than 2 weeks during the intervention period

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Lucerne, Faculty of Health Sciences and Medicine, University Research Centre Health and Society

Lucerne, Canton of Lucerne, Switzerland, 6002

Actively Recruiting

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Research Team

C

Claudio Perret, PhD

CONTACT

A

Andrea M Aegerter, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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