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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05042115
Other study ID # 43063621.3.0000.8123
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 10, 2022
Est. completion date February 28, 2023

Study information

Verified date March 2024
Source Instituto Docusse de Osteopatia e Terapia Manual
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

INTRODUCTION: Chronic low back pain (CLBD) is one of the major public health problems in the world. Given the complexity of the situation, complementary and alternative practices such as pain neuroscience education (PNE), clinical hypnosis (HC) and osteopathic manipulative treatment (OMT) are options for we manage these patients. OBJECTIVE: The aim of this study will be to evaluate the effects of OMT associated with PNE through HC on pain and disability in patients with CLBP compared to PNE and HC. MATERIALS AND METHODS: The study design will be a randomized clinical trial and 40 adults diagnosed with chronic low back pain will be recruited. Subjects will be randomized in two groups: the first group (G1) will be submitted to the PNE based on information from the book "Explain Pain" with hypnotic suggestions. Group 2 (G2) will receive PNE following the book "Explain Pain" with hypnotic suggestions associated with OMT. Volunteers will be evaluated by a blind researcher the interventions performed in the allocation of groups. The evaluation moments will be pre-intervention and immediately after the end of the last intervention for G1 and G2. Volunteers continued to be evaluated 4 weeks after completion of the protocols. Pain will be evaluated as the main outcome, being evaluated by the numerical pain scale. Pain will also be assessed by the pressure threshold using a pressure algometer device (Fnd-50, PIAB 50-n, Italy) in the lumbar region. Still as the main outcome, disability will be assessed using the Oswestry Disability Questionnaire. As secondary outcomes, the patient's global impression of improvement, central sensitization, biopsychosocial factors will be evaluated. The patient's global impression of improvement will be assessed using the Percentage of Improvement Scale with a score of -5 to +5; the Central Sensitization will be assessed using the Central Sensitization Questionnaire and the biopsychosocial factors using the Start Beck Toll questionnaire. In addition, the behavior of the autonomic nervous system will be evaluated through the Heart Rate Variability (HRV), which will be analyzed through linear methods, in the domains of time and frequency, and by geometric indices. The researcher/evaluator will be blinded to the allocation of intervention groups. Given the nature of the study, it is impossible to blind the researcher/therapist and volunteers.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date February 28, 2023
Est. primary completion date November 30, 2022
Accepts healthy volunteers No
Gender All
Age group 30 Years to 60 Years
Eligibility Inclusion Criteria: - Nonspecific Low Back Pain for at least 3 months - Score on the numerical pain scale of at least 3 points Exclusion Criteria: - Data from participants with less than 95% of sinus beats - Participants that present increased symptoms in any stages of the study - Patients who are undergoing concomitant physical therapy treatment, patients with contraindications to exercise, smokers/alcoholics, severe vertebral or neural pathologies, previous spine surgeries, cardiorespiratory disease, LBP as a secondary complaint, pregnancy, hearing problems, or illiteracy patients, not will are able to participate the protocol.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Education in pain neurosciences and clinical hypnosis
Will be performed education in pain neurosciences and clinical hypnosis, in 4 sessions during 4 weeks
Education in pain neurosciences and clinical hypnosis plus osteopathic manipulative treatment
Will be performed education in pain neurosciences and clinical hypnosis, and only for this group will be delivered osteopathic manipulative treatment, in 4 sessions during 4 weeks

Locations

Country Name City State
Brazil Anne Kastelianne Presidente Prudente São Paulo

Sponsors (2)

Lead Sponsor Collaborator
Instituto Docusse de Osteopatia e Terapia Manual Universidade Estadual do Norte do Paraná

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain perception The Pain suffered in the last week will be assessed by the Numerical pain scale, with a range of 0 - 10 T0= before the protocol; T1= until 24 hours after the end protocol; T2= four weeks after end protocols
Primary Pain pressure threshold Pain will be assessed by the pressure threshold using a pressure algometer device in the lumbar region. The assessment will be conducted specifically in the paravertebral muscles bilaterally at levels L1 to L5. T0= before the protocol; T1= until 24 hours after the end protocol; T2= four weeks after end protocols
Primary Disability Disability will be assessed using the Oswestry Disability Questionnaire T0= before the protocol; T1= until 24 hours after the end protocol; T2= four weeks after end protocols
Secondary Patient's global impression of improvement The patient's global impression of improvement will be assessed using the Percentage of Improvement Scale with a score of -5 to +5 T0= before the protocol; T1= until 24 hours after the end protocol; T2= four weeks after end protocols
Secondary Central Sensitization and biopsychosocial factors The Central Sensitization Questionnaire and the biopsychosocial factors will be assessed using the Start Beck Toll questionnaire T0= before the protocol; T1= until 24 hours after the end protocol; T2= four weeks after end protocols
Secondary Heart Rate Variability Heart Rate Variability, which will be analyzed through linear methods, in the domains of time and frequency, and by geometric indices T0= before the protocol; T1= until 24 hours after the end protocol; T2= four weeks after end protocols
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