Cognitive Rehabilitation for Veterans With PNES

Part of paid clinical trials in Providence, Rhode Island.

Sponsor
VA Office of Research and Development
Study ID
NCT07316543
Status
Recruiting

Conditions

  • Psychogenic Nonepileptic Seizures (PNES)

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Cognitive Rehabilitation And Functional Treatment (CRAFT) — BEHAVIORAL
    Cognitive rehabilitation tailored to improve cognition and participation in daily activities for Veterans with PNES

Study Details

Psychogenic nonepileptic seizures (PNES) reflect a subtype of functional neurological disorder (FND) that is common and extremely disabling in Veterans. Cognitive problems are highly prevalent in PNES, they reduce quality of life, and they severely limit daily functioning. Currently, there are no available treatments that target cognition to improve daily function in PNES or other FNDs, leaving a major gap in the literature. Cognitive re-habilitation improves daily functioning in Veterans with related neuropsychiatric disorders and has a high chance of success in Veterans with PNES. The proposed study will solicit direct input from Veterans with PNES via qualitative interviews to inform the design of a cognitive treatment workbook. The workbook will then be iteratively refined based on participatory feedback from Veterans with PNES and their treatment providers. The full cognitive intervention protocol will be pilot tested to inform a fully powered RCT. Results will support a line of research that aims to improve cognition and function in Veterans with PNES and related FNDs.

Key Dates

Start date
Mar 2, 2026
Status verified
Mar 2026
Primary completion
Jul 1, 2031
Completion
Jul 1, 2031

Study Design

Enrollment
47 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Other: Intervention
    Single arm of pilot trial testing the cognitive rehabilitation intervention

Primary Outcome Measure

WHODAS 2.0 Total Score [ Time Frame: Once at baseline (prior to the intervention) and once following the 8-12 week intervention. ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Providence VA Medical Center, Providence, RIProvidenceRhode Island02908-4734
Kimberly Marcolivio, MEd CCRP
401-273-7100
Kate J Barnabe, MHA
(401) 273-7100
Ryan A Van Patten, PhD (PRINCIPAL_INVESTIGATOR)

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