- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06695806
Measurement of the Intolerance to Uncertainty in Osteopaths
Measurement and Evolution of the Intolerance to Uncertainty in Osteopaths and Osteopathic Students: a Longitudinal Study
Clinical reasoning is a challenging, complex, multi-dimensional, essentially introspective and poorly understood cognitive process, as well as a crucial skill for osteopaths and health professionals. It can be agreed that this includes diagnosing the patient's condition, making therapeutic decisions to improve that condition, and the practitioner's ability to assess the patient's prognosis. Individual clinical expertise is acquired through experience. Each healthcare professional develops their own approach to problem-solving and decision-making, influenced by factors such as personality, preferences, clinical perception, and professional practices. It is important to be aware that certain factors can influence their judgement and potentially affect the quality of their work. It is possible that certain factors may influence their judgement and potentially lead to errors in their decision-making, as they can be influenced by cognitive biases such as intolerance of uncertainty. Uncertainty intolerance is defined as a personal disposition characterised by negative beliefs about uncertainty and its consequences, coupled with an underlying apprehension about the unknown. Uncertainty affects the behaviour of individuals by creating a need for certainty, which in turn affects the clinical reasoning and decision-making of healthcare professionals.
The objective of this study is to assess the level of intolerance to uncertainty among osteopathic students and osteopaths using an online self-report questionnaire. A second questionnaire will be sent out six months after the first, allowing to assess individual changes in this intolerance over time. Furthermore, the impact of being a graduate, anxiety and the type of osteopath responding to the questionnaire will be examined. The final measure will be evaluated using a classification method called latent class analysis. This will be based on responses to questions about their relationship to evidence-based practice, dogmatism and their thoughts about the impact of osteopathic treatment.
The aim of this study is to carry out a psychometric validation of the intolerance to uncertainty questionnaire on a population of osteopaths.
Study Overview
Status
Conditions
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
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-
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saint Herblain, France, 44800
- IDHEO nantes
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Student in osteopathy (3rd, 4th or 5th year) or have a diploma in osteopathy
- Provide an informed consent
Exclusion Criteria:
- Patients refusing to take part in the study.
- Pregnant women
- Patients under legal protection
- Patients who are protected adults or adults unable to express their consent.
- Withdrawal of consent to participate in the study
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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osteopath
Participants should be osteopaths or students in osteopathy.
They need to understand french and give their consent before answering questionnaire.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Intolerance to uncertainty
Time Frame: at enrollement
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Total score of the questionnaire: Intolerance of Uncertainty Scale in Health (IUS-12-H), consisting of 12 questions.
Participants answer on a Likert scale ranging from "not at all characteristic of me" (1), "somewhat characteristic of me" (2), "somewhat characteristic of me" (3), "very characteristic of me" (4), and "very characteristic of me" (5).
The score ranges from 12 (no intolerance of uncertainty) to 60 (great intolerance of uncertainty).
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at enrollement
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Change in Intolerance to uncertainty
Time Frame: From enrollement to the second assessment, six mounth later.
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From enrollement to the second assessment, six mounth later.
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Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- MICO
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ANALYTIC_CODE
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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