Efficacy of Pain Neuroscience Education and Pre-anesthetic Assessment in Reducing Levels of Anxiety, Stress and Pain in Patients Undergoing Elective Total Abdominal Hysterectomy (ENAH Study)

I

Instituto Neurociencia Del Dolor

Status

Enrolling

Conditions

Surgery
Pain, Postoperative
Pain, Chronic
Anxiety
Stress
Anesthesia

Treatments

Other: Usual care
Other: Pain Neuroscience Education

Study type

Interventional

Funder types

Other

Identifiers

NCT05435508
INeurocienciaDolor

Details and patient eligibility

About

Through this quantitative, multivariate factorial experimental research of the Parallel Randomized Clinical Trial type, the investigators will try to analyze the effectiveness in reducing levels of anxiety, stress and pain through pre-anesthetic assessment and pain neuroscience education in patients undergoing elective total abdominal hysterectomy.

Full description

Hysterectomy is a common surgical procedure with a low risk of major complications. However, some women experience long-lasting complications, including chronic postsurgical pain, which can have a negative impact on their quality of life. The population will be made up of women with elective total abdominal hysterectomy scheduled surgery at the University Hospital of Puebla BUAP, in the city of Puebla, Mexico. Then the investigators will carry out an pre-anesthetic evaluation will be carried out and an pain neuroscience education session will be carried out. Once patients are ready for surgery, the investigators will carry out an invasive monitoring will be performed in the post-anesthesia care unit. The blood pressure of the participants will be monitored non-invasively. They will also be monitored with electrocardiogram and pulse oximetry.

Enrollment

62 estimated patients

Sex

Female

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Anesthesia Physical Classification System: I, II or III according to the classification of the American Society of Anesthesiology.
  • Acceptance of informed consent
  • Schooling of at least 12 years (basic primary and secondary).

Exclusion criteria

  • Illiterate
  • Inflammatory rheumatic disease
  • Major neurological or psychiatric disease, Intellectual disability (mental retardation) or learning disorders at the premorbid level or severe language comprehension problems.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

62 participants in 2 patient groups

Pain Neurosicence Education + Pre-anesthetic Assessment
Experimental group
Description:
Pain neuroscience education + Pre-anesthetic Assessment. Pain neuroscience education can be defined as an educational session or sessions describing the neurobiology and neurophysiology of pain, and pain processing by the nervous system.
Treatment:
Other: Pain Neuroscience Education
Pre-anesthetic Assessment (Usual Care)
Other group
Description:
The pre-anesthetic assessment is the clinical study that allows evaluating the physical condition, personal, pathological and surgical history together with laboratory tests to be able to establish a surgical risk in order to define the best anesthetic plan that the patient requires according to the surgical event.
Treatment:
Other: Usual care

Trial contacts and locations

1

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Central trial contact

Julio Cesar Pablo Yañez, MD; Miguel Calva Maldonado, MD

Data sourced from clinicaltrials.gov

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