Expired Study
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San Francisco, California 94111


Purpose:

This study is a validation study to document the acceptability of the Tonic and Phasic Alertness Training (TAPAT) program in older adults with chronic late-life insomnia. The goal of this study is to employ a computerized attention-training program, TAPAT, designed for chronic late-life insomnia in a remote, randomized, controlled trial to assess feasibility and initial efficacy in this population.


Criteria:

Inclusion Criteria: - Participant must be 55 years of age or older. - Participant must meet criteria for clinical insomnia - moderate severity based on the Insomnia Severity Index. - Participant must be a fluent English speaker. - Participant must have adequate visual, auditory, and motor capacity to use computerized intervention. - Participant must have a computer and access to the Internet. Exclusion Criteria: - Participants with untreated psychiatric conditions, including substance abuse/dependence disorders, untreated obstructive sleep apnea, diagnosis of other sleep disorders (e.g., restless legs syndrome), recent hospitalization, ongoing chemotherapy or other cancer treatment, and concurrent engagement in another insomnia treatment. - Participants enrolled in another concurrent research study. - Participants using computer-based cognitive training programs or has used them within a month of the consent date.


NCT ID:

NCT03604380


Primary Contact:

Principal Investigator
Thomas Van Vleet, PhD
Posit Science Corporation


Backup Contact:

N/A


Location Contact:

San Francisco, California 94111
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: February 04, 2019

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