Epilepsy Clinical Trial
Official title:
A Pilot Study of Creative Arts Interventions for Neurology Inpatients in the Epilepsy Monitoring Unit and the Headache Service
NCT number | NCT03520777 |
Other study ID # | 30498 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | September 19, 2017 |
Est. completion date | June 30, 2018 |
Verified date | July 2018 |
Source | Dartmouth-Hitchcock Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of the study is to assess the feasibility of a Creative Artists Program intervention with epilepsy and headache patients admitted to Dartmouth-Hitchcock Medical Center for care by the Department of Neurology.
Status | Completed |
Enrollment | 33 |
Est. completion date | June 30, 2018 |
Est. primary completion date | June 1, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: 1. Age > or = 18 years 2. Diagnosis of refractory chronic epilepsy, status migrainosus, or chronic daily headache 3. Elective admission to the Dartmouth-Hitchcock Medical Center Epilepsy monitoring unit or Headache service 4. Capable of giving informed consent Exclusion Criteria: 1. Active psychiatric illness that prohibits safe visitation by artists 2. Impairment of vision or hearing that would prohibit able to participate with participation in instructions necessary for the interventions. 3. Active general medical condition that would impair consciousness. |
Country | Name | City | State |
---|---|---|---|
United States | Dartmouth-Hitchcock Medical Center | Lebanon | New Hampshire |
Lead Sponsor | Collaborator |
---|---|
Dartmouth-Hitchcock Medical Center |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Feasibility of conducting a creative arts intervention study | The feasibility of the creative intervention will be determined by the completion rates of the initial intervention attempts. If less than 50% of patients complete the intervention it will be deemed unfeasible in the current format. | Through study completion, approximately 1 year | |
Secondary | Change in patient anxiety before and after the intervention | Change in anxiety level will be calculated, based on patient questionnaire responses, following the creative intervention. | Each patient will be assessed at baseline (Day 1) and after the intervention (approximately Day 3 - 21). | |
Secondary | Change in patient distress before and after the intervention | Change in distress level will be calculated, based on patient questionnaire responses, following the creative intervention. | Each patient will be assessed at baseline (Day 1) and after the intervention (approximately Day 3 - 21). | |
Secondary | Change in patient depression before and after the intervention | Change in depression level will be calculated, based on patient questionnaire responses, following the creative intervention. | Each patient will be assessed at baseline (Day 1) and after the intervention (approximately Day 3 - 21). | |
Secondary | Change in frequency of as-needed pain medication use | As-needed pain medication utilization will be evaluated following the creative arts intervention through subject discharge. | Each patient as-needed medication use will be assessed after the arts intervention and until discharge from the hospital (approximately Day 3 - 21). | |
Secondary | Length of hospital stay | Length of hospital stay will be calculated. | Each patient's admission duration (approximately 3 - 21 Days). |
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