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 @ 11:42 PM
Ignite Modification Date:
2025-12-24 @ 11:42 PM
NCT ID:
NCT01182051
Eligibility Criteria:
Inclusion Criteria:
* To determine eligibility, youth will complete an evaluation consisting of clinical interviews, self-, and parent-report measures.
* To be included in the study, all children must:
1. have a current diagnosis of chronic daily headache, tension-type headache, and/or migraine headache
2. obtain a total score on the Screen for Child Anxiety Related Disorders (SCARED) in the clinical range (i.e., \> 20)
3. be between 7 and 17 years old
4. have a parent/guardian who gives consent and agrees to participate
5. be English speaking
6. not currently participating in other psychosocial treatments specifically directed at reducing head pain or anxiety.
* For youth receiving prophylactic medication, it is preferable that they remain on a stable dose and agree to avoid medication changes while enrolled in the study. Thus, all participants will be permitted to continue with their prescribed medical/neurological treatment, however the use of medications (both prophylactic and over-the-counter analgesics) will be closely monitored.
Exclusion Criteria:
* Youth will be excluded from the study if they have a medical or psychiatric condition contraindicating study treatment or warranting an alternative intervention (e.g., suicidality, depression).
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
7 Years
Maximum Age:
17 Years
Study:
NCT01182051
Study Brief:
Protocol Section:
NCT01182051