Low Back Pain Clinical Trial
Official title:
The Influence of a Biopsychosocial Educational Internet-based Intervention on Pain, Dysfunction, Quality of Life, and Pain Cognition in Chronic Low Back Pain Patients in Primary Care: a Mixed Methods Approach
Aim: The aim of this project is to identify chronic low back pain patients´ beliefs about the
origin and meaning of pain for developing a biopsychosocial web-based educational
intervention. The other aim of this project is to assess the effectiveness of this web-based
educational intervention for chronic low back pain patients on pain cognitions, pain
intensity, and disability.
Methods: Mixed methods design, combining both qualitative and quantitative methodologies. For
the qualitative part of this study, the investigators will use qualitative in-depth
semi-structured interviews. For the quantitative phase we will use an experimental study
design.
Subjects: Chronic low back pain patients between 18-65 years old, attending a primary care
setting in the city of Lleida.
Expected outcomes: The investigators expect to change and modify chronic low back pain
patients´ cognition by using our web-site educational intervention, with the further outcome
of reducing pain and disability.
Hypothesis and outcomes
Hypothesis:
1. Persistent chronic low back pain and its consequences are maintained by the lack of
understanding about the origin and meaning of pain.
2. Pain neurophysiology as an educational internet- based intervention for chronic low back
pain will change cognition about the origin and meaning of pain, with the outcome of
pain reduction, disability reduction, and better quality of life compared to normal
care.
Outcomes:
There are specific objectives for each phase of the study.
Phase 1 (QUAL):
To identify chronic low back pain patients' beliefs concerning the origin and meaning of
pain.
Phase 2 (Connecting procedure):
To construct and develop a biopsychosocial web- based educational intervention using the QUAL
results.
Phase 2 (QUAN):
Primary outcome. To evaluate the effect of a biopsychosocial web-based educational
intervention for chronic low back pain based on pain intensity compared to normal care.
Secondary outcomes. To assess the effect of a biopsychosocial web-based educational
intervention for chronic low back pain compared to normal care on:
- Fear avoidance beliefs.
- Kinesiophobia.
- Disability.
Methodology Study design
To answer the research question, the authors will use a mixed-method sequential exploratory
design. The pur- pose of mixed methodology is not to replace qualitative or quantitative
methodologies, but to use the strengths of both while reducing their weaknesses. Specific-
ally, the sequential exploratory design includes an initial qualitative phase followed by a
quantitative phase, with the aim of developing an educational tool. In this project, we
propose that both phases (qualitative and quantitative) must have the same relevance (QUAL-
QUAN) for the development of the educational tool and that the development of the study must
be conducted in three stages:
1. Qualitative data collection through semi-structured personal interviews followed by
thematic analysis.
2. Construction of the educational tool with the results obtained in the previous step
(topics or emerging categories).
3. Analysis of the effectiveness of the educational tool using a randomized controlled
trial.
Scope: Primary care
SUBJECTS:
The recruitment process will be performed independently in each phase of the study, although
in both phases this recruitment process will take place in the same pri- mary care centers in
the city of Lleida through family physicians. The inclusion and exclusion criteria are also
common to both phases. Prior to the beginning of the first phase, the first author of this
study will perform a presentation of the project to the medical and nursing staff in each of
the primary care centers involved in the study to ask for their cooperation.
QUAL: In this phase, patients will be recruited by their respective family physicians. Once
the physician makes the diagnosis of CLBP and ensures that the individual meets the inclusion
and exclusion criteria, the physician informs the patient about the existence of this project
and invites him to contact the first author by telephone. If the person agrees to participate
in the study, the inter- view will be scheduled to take place in the Faculty of Nursing and
Physiotherapy of the University of Lleida.
QUAN: The recruitment process will start after the end of QUAL and the development of the
educational tool. This phase will consist of an educational interven- tion using a randomized
controlled trial design. The re- cruitment process will be the same as in QUAL. Prior to the
beginning of the intervention, the first author will meet the study subjects individually to
inform them of the study conditions and provide them with the informed consent form.
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