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Enrolling by invitation NCT06684665

Study on the Sociopsychoemotional Mechanism of Dysfunction in Patients With Acute and Chronic Low Back Pain

Observational Low Back Pain

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Low Back Pain. Basic parameters: 18 years — 75 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Introduction;Epidemiology;Socioeconomic Burden

Overview

Low back pain is defined as pain that extends from the 12th rib to the iliac bone, and its increasing incidence makes it one of the major causes of decreased productivity worldwide. Dysfunction is one of the important complications in patients with chronic low back pain, and related studies have shown that depression, pain catastrophization and other emotions can affect the occurrence and development of dysfunction. So the investigators wanted to study which psychological emotions affect the development of dysfunction in patients with low back pain.

Primary outcome measures

  • Dysfunction index of patients with acute and chronic low back pain [Time frame: From enrollment to 2 months later]

Eligibility criteria

Inclusion criteria

  • Age 18-75;
  • Patients with low back pain;
  • Have good communication skills to ensure the collection of scale information

Exclusion criteria

  • Suffering from severe mental or psychiatric disorders.;
  • Unwilling to participate in the interview;
  • Patients with pain in other areas

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Case-control

Study locations

China · 1 center
  • The Second Affiliated Hospital of Wenzhou Medical University — Wenzhou

Identifiers

NCT: NCT06684665 · SAHoWMU-CR2024-13-219

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗