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The effect of health education on the patient with chronic pain

Effect of a health education program on individuals with chronic pain

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-6fyh2c
Enrollment
Unknown
Registered
2018-07-31
Start date
2018-04-10
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Pain

Interventions

1. Design and Target Population: A Randomized Clinical Trial (RCT) will be performed with people who present chronic pain in a community attached to the Pituaçu and Pituaçu Park Health Units, Boca do
Other
I02.233.332

Sponsors

Escola Bahiana de Medicina e Saúde Pública
Lead Sponsor
Escola Bahiana de Medicina e Saúde Pública
Collaborator

Eligibility

Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Individuals enrolled in the health teams of the Pituaçu family health units and Pituaçu Park; daily or near-daily pain for at least six months; between the ages of 18 and 60; who were literate.

Exclusion criteria

Exclusion criteria: Pregnant women; people with difficulties to understand the questionnaires; associated diseases that can reduce the level of quality of life;functional illiteracy.

Design outcomes

Primary

MeasureTime frame
Reduce pain intensity in four points on the Visual Analogue Pain Scale in individuals with chronic pain who participated in the health education program. The pain evaluation will be performed from the instruments that characterize the pain: Brief Pain Inventory and Visual Analog Pain Scale. This evaluation will happen in the pre and post test and will be performed with the 62 patients, in a time interval of 6 months.

Secondary

MeasureTime frame
To improve the quality of life of individuals with chronic pain who participated in the health education program. The quality of life will be assessed using the World Health Organization Quality of Life Scale. This evaluation will be carried out in the pre- and post-test and will be performed with the 62 patients, in a time interval of 6 months.

Countries

Brazil

Contacts

Public ContactAna Shirley;Ana Shirley Maranhão Vieira;Maranhão Vieira

Escola Bahiana de Medicina e Saúde Pública;Escola Bahiana de Medicina e Saúde Pública

asmvieira@bahiana.edu.br;asmvieira@bahiana.edu.br+5571992068617;+5571992068617

Outcome results

None listed

Source: REBEC (via WHO ICTRP)