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http://eprints.org/relation/isVersionOf https://researchdata.bath.ac.uk/id/document/11123 http://eprints.org/relation/isVolatileVersionOf https://researchdata.bath.ac.uk/id/document/11123 http://eprints.org/relation/isIndexCodesVersionOf https://researchdata.bath.ac.uk/id/document/11123 archive 6772 disk0/00/00/05/16 2019-03-22 09:24:52 2024-06-18 10:00:33 2019-03-22 09:24:52 data_collection show Tabor Abby A.Tabor@bath.ac.uk University of Bath TRUE Researcher Eccleston Christopher C.Eccleston@bath.ac.uk 0000-0003-0698-1543 University of Bath Researcher Vollaard Niels 0000-0002-4576-8879 University of Stirling Researcher Keogh Edmund E.M.Keogh@bath.ac.uk 0000-0002-1615-3699 University of Bath JN0010 dept_health dept_psy This data set includes all data associated with the study, "Taking aversive action: an experimental investigation into the negotiation of bodily limits." The data include Gender, Age, BMI and Activity levels (IPAQ). In addition they include all data associated with the main variables of the study, including Interoceptive Accuracy, Heart Rate Variability, Anxiety Sensitivity, Porges Body awareness, and Mean Power Output. Absolute difference scores are provided for time intervals 1, 2, and 3. 2019-03-22 University of Bath public RightsHolder University of Bath Reckitt Benckiser Healthcare https://doi.org/10.13039/100013207 BATHTAP: Further Developments in a Test of Attention to Pain Thirty-eight participants (19F; Mean age: 23y; SD±4y) were recruited from a university campus through poster and electronic advertisement. All participants were screened for their health and activity level via the International Physical Activity Questionnaire (IPAQ short form) prior to the initiation of the study (Appendix. 1): only participants determined to be inactive (performed less than 3 x 20 minutes of vigorous exercise per week; <600 MET minutes) and otherwise healthy met the inclusion criteria (Total screened=40; two excluded due to activity levels). Participants were excluded if they had previously completed the maximal exercise tasks, were currently experiencing pain or had a history of pain lasting more than 3 months (full exclusion criteria: diagnosed cardiovascular disease, diagnosed respiratory disorder [COPD; cystic fibrosis] or neurological disorder [TIA, infarction/haemorrhage, cerebral palsy or neurological deficit], diagnosed psychiatric disorders [major depressive disorder; schizophrenia, bipolar]). This study was conducted in accordance with the declaration of Helsinki and ethical approval was obtained from divisions of Health and Psychology. All 38 participants provided written, informed consent. Participants were required to complete two separate sessions: first a baseline session and then a test session, with a minimum of 24 hours’ rest between each one. For the total duration of both sessions, participants wore a heart rate monitor, which was connected to a Polar V800 watch. All participants were asked to abstain from alcohol and caffeine in the preceding 24-hours of the baseline and test sessions. en 1 10.15125/BATH-00516 https://doi.org/10.1371/journal.pone.0210853 pub