Actively Recruiting

Age: 18Years +
All Genders
ID06915896

Predictive Variables of Outcome in Subjects With Chronic Rachialgia Referred to Different Pathways of Physiotherapy: Multicenter Prospective Study

Led by Fondazione Don Carlo Gnocchi Onlus · Updated on 2025-04-08

200

Participants Needed

1

Research Sites

12 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying people with chronic non-specific low back pain or neck pain who are undergoing public health rehabilitation. The study aims to find out which biopsychosocial factors can predict how well patients recover and to check the reliability of certain patient questionnaires used to evaluate spinal pain. These questionnaires have not yet had their measurement properties fully established in this population. Participants will take part in two main assessment sessions: one before starting rehabilitation and one after completing it. There is also a re-test session immediately before rehabilitation to evaluate questionnaire reliability in stable patients. Follow-up assessments occur at 3 and 6 months after discharge to monitor ongoing outcomes. During the study, participants will complete various questionnaires and scales related to disability, pain intensity, quality of life, pain awareness, sleep quality, and medication use. Researchers will measure key outcomes such as the Neck Disability Index and Roland and Morris Disability Questionnaire at multiple time points. This study will help understand which factors influence recovery and how well the questionnaires perform over time.

CONDITIONS

Brief Title

Predictive Variables of Outcome in Subjects With Chronic Rachialgia Referred to Different Pathways of Physiotherapy.

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Medical diagnosis of nonspecific low back pain or nonspecific neck pain
  • Symptoms present for at least 6 months
  • Waiting for rehabilitation in a public health program
  • Signed informed consent for participation and data processing
Not Eligible

You will not qualify if you...

  • Cognitive impairment that affects memory or understanding

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - 6 months

Participants are observed while attending public health rehabilitation pathways for chronic spinal pain.

3 visits at enrollment, 3 months, and 6 months

Trial Site Locations

Total: 1 location

1

IRCCS Fondazione Don Carlo Gnocchi, Firenze

Florence, FI, Italy, 50124

Actively Recruiting

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Research Team

F

Francesca Cecchi

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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