Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 6:31 PM
Ignite Modification Date:
2025-12-24 @ 6:31 PM
NCT ID:
NCT06606457
Eligibility Criteria:
Inclusion Criteria:
1. diagnosis of CF;
2. age \> 18 years;
3. report of pain affecting them at least moderately (score ≥ 2) on the IPOS item;
4. pain lasting at least one month;
5. English-speaking;
6. participant willing and able to give informed consent.
Exclusion Criteria:
Presenting an acute safety risk to self or others at baseline. Participants will not be excluded for the following reasons:
1. CF severity or lung/liver transplant status, if they are otherwise able to participate in CBT;
2. Participation in concomitant pain treatments (e.g., pain medications), as ideally, patients will engage in multi-component pain interventions;
3. psychosocial treatments (with the exception of another formal CBT for pain) or psychopharmacologic treatments at baseline. All concomitant psychosocial and pain-directed treatments will be tracked and considered in analysis.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT06606457
Study Brief:
Protocol Section:
NCT06606457