Pain in Subjects with High Capacity Cognitive Abilities
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: High Cognitive Abilities, Pain, Prevalence. Basic parameters: No limits · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Spain
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Pain in Subjects with High Capacity Cognitive Abilities: a Cross Sectional Study
Overview
In many books and website focused in high cognitive abilities talks about pain in these subjects. However, when the investigators look for in sites like pubmed there are no literature about this topic. With this study the investigators will try to know better pain experience in this population and chronic pain prevalence
Detailed description
It's said that people with high cognitive abilities suffered pain. However, there are no scientific literature. With this study the investigators would like to know better pain experience in this population. There are two target groups include inside this population that we consider to study: Children population and adults population.
The aim of this study is to know the prevalence of chronic pain in this population and to analize the pain experience of this population and the related psychosocial variables that can modify it, like catastrophicing, kinesiophobia, anxiety, quality of life and level of physical activity,
The investigators will use a questionnaire that includes different questionnaires like TSK-11SV, PCS, STAI, SF-36 and IPAQ and many question to evaluate the demographic factor of the sample and the prevalence
The investigators will do an statistical analysis to observe the relationship and the predictors factors
Primary outcome measures
- Perceived quality of life [Time frame: 1 day]
Secondary outcome measures (4)
- Kinesiophobia [Time frame: 1 day]
- Catastrophising [Time frame: 1 day]
- Anxiety [Time frame: 1 day]
- Physical activity [Time frame: 1 day]
Eligibility criteria
Inclusion criteria
- People with a diagnosis of high cognitive abilities
Exclusion criteria
- People with incapacity to answer the questionnaire
- People that's not have a good level of Spanish language
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Observational model
- Case-only
Study locations
Spain · 1 center
- Universidad Europea de Madrid — Villaviciosa de Odón
Identifiers
NCT: NCT06695351 · GIFTEDNESS_Pain