HOBSCOTCH Phase II

Completed · Not applicable

Conditions studied: Epilepsy

In brief

The purpose of this study is to determine the feasibility and efficacy of the home-based cognitive self-management program "HOBSCOTCH" delivered at four New England medical centers. It will test the long-term impact and cost-effectiveness of HOBSCOTCH, and whether it can be delivered from a distance utilizing e-health tools for parts of the program.

Key facts

Study ID

NCT02394509

Run by

Dartmouth-Hitchcock Medical Center

People needed

106

Starts

2015-03-01

Expected to finish

2019-09-01

Last updated by the study team

2020-08-20

Who can join

Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age 18-70
• Confirmed diagnosis of epilepsy, with controlled or uncontrolled seizures
• Subjective memory complaints
• No changes in antiepileptic and antidepressant medication regimen for 1 month, however brief discontinuation of antiepileptic medicine for inpatient video EEG evaluation is acceptable
• Literate
• Telephone access

You may not qualify if…

• Subjects age 66-70 with a mention of a dementing illness in their medical record
• Severe mental disability or estimated IQ less than 70
• Significant visual impairment precluding reading or writing
• No reliable telephone access

Where it is running

• Maine Medical Center — Portland, Maine, United States
• University of Massachusetts Medical School — Worcester, Massachusetts, United States
• Dartmouth-Hitchcock Medical Center in Lebanon, NH — Lebanon, New Hampshire, United States
• University of Vermont Medical Center — Burlington, Vermont, United States

Full record on ClinicalTrials.gov

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