Evidence map›Paper›PMID 41361715›Full record

Trial reportAnnals of clinical and translational neurology2026

Lessons Learned From a Delayed-Start Trial of Modafinil for Freezing of Gait in Parkinson's Disease.

Tuhin Virmani, Lakshmi Pillai, Reid D Landes, Aliyah Glover, Shannon Doerhoff, Jennifer Kleiner, Mitesh Lotia, Rohit Dhall, Edgar Garcia-Rill

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Annals of clinical and translational neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Tuhin VirmaniDepartment of Neurology, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.ORCID 0000-0002-1826-2020
Lakshmi PillaiDepartment of Neurology, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Reid D LandesDepartment of Biostatistics, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Aliyah GloverDepartment of Neurology, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Shannon DoerhoffDepartment of Neurology, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Jennifer KleinerDepartment of Psychiatry, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Mitesh LotiaDepartment of Neurology, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Rohit DhallDepartment of Neurology, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Edgar Garcia-RillCenter for Translational Neuroscience, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.

Funding

NIGMS NIH HHS GM110702Parkinson's Foundation PF-JFA-1935University of Arkansas for Medical Sciences
6 · The paper itself

Abstract

objectiveFreezing of gait (FOG) in people with Parkinson's disease (PwPD) is debilitating and has limited treatments. Modafinil modulates beta/gamma band activity in the pedunculopontine nucleus (PPN), like PPN deep brain stimulation. We therefore tested the hypothesis that Modafinil would improve FOG in PwPD.

methodsPwPD with FOG were randomized to early-start (24 weeks modafinil) or delayed-start (12 weeks each, placebo then modafinil) of oral modafinil 50 mg, followed by a 2-week washout for both arms. Primary outcomes were change in OFF-levodopa stride length and FOG questionnaire scores; secondary outcomes were change in motor Unified Parkinson's Disease Rating Scale (UPDRS), sleep and quality-of-life scores, and post hoc outcome was change in percent freezing time (%FT).

resultsEarly- (n = 12) and delayed-start (n = 9) group participants were well matched for age, OFF-levodopa motor UPDRS and FOG-Q scores. Primary and secondary outcomes did not reach statistical significance. Limiting the analysis to study completers with quantifiable visualized freezing at the initial visit and collapsing the two study arms (n = 11), %FT trended to improvement with 50 mg modafinil in 8/11 participants (p = 0.15) and worsening after 2 weeks washout in 9/11 participants (p = 0.09). A future cross-over study with 50 participants would have 0.80 power to detect a 0.5 standard-deviation improvement in %FT.

interpretationFor future therapeutic trials, selecting PwPD with moderate, quantifiable FOG and utilizing appropriate outcome measures like %FT will improve the ability to identify intervention effects. Even for short trials, analyses must account for gait decline. An FOG outcome measure that requires less analysis time burden than video quantification, and the ability for at-home monitoring is needed.

Indexed as

Gait Disorders, NeurologicModafinilOutcome Assessment, Health CareParkinson DiseaseWakefulness-Promoting AgentsAgedDouble-Blind MethodFemaleHumansMaleMiddle AgedModafinilWakefulness-Promoting Agentsclinical trialdelayed‐start designfreezing of gaitParkinson's diseasevideo‐based gait quantification

Identifiers

PMID41361715
PMCPMC13161890

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.