ACTRN12624000407594
Not yet recruiting
未知
Investigating the effectiveness of mindfulness meditation and clinical hypnosis for injury-related pain management in competitive athletes: A replicated single-case experimental design
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Pain, Acute
- Sponsor
- The University of Queensland
- Enrollment
- 18
- Status
- Not yet recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •a) be a competitive athlete (i.e., compete at a level beyond recreational or casual participation. This includes athletes who participate in regional, national, or international competitions, and those who are members of competitive teams or clubs),
- •b) currently have a sport or exercise\-related injury that resulted in an average pain
- •intensity greater than or equal to 3 on a 0\-10 numerical rating scale in the past
- •week, and for which the predicted recovery time at the point of study enrolment is
- •greater than 5 weeks
- •c) be 18 years of age or over,
- •d) read, speak, and understand the English language,
- •e) have access to the internet on a computer or smartphone,
- •f) have access to a set of earphones,
- •g) be willing to be randomly assigned to both conditions and listen to five 20\-minute treatment sessions (one per day),
Exclusion Criteria
- •a) Current alcohol or substance dependence;
- •b) Pain condition for which surgery has been recommended and is planned;
- •c) Current or past participation in a research study with treatment components that may overlap those in the current study;
- •d) Current or history of diagnosis of primary psychotic or major thought disorder within the past 5 years;
- •e) Psychiatric hospitalization within the past 6 months;
- •f) Psychiatric or behavioural conditions in which symptoms were unstable or severe within the past 6 months;
- •g) Active malignancy (e.g., cancer not in remission), terminal illnesses, or serious medical conditions that may interfere with either study participation or with receiving potential treatment benefits (e.g., severe lupus).
Outcomes
Primary Outcomes
Not specified
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