Evidence map›Paper›PMID 38494550›Full record

Trial reportPsychopharmacology2024

The effects of pramipexole on motivational vigour during a saccade task: a placebo-controlled study in healthy adults.

Sheena K Au-Yeung, Don Chamith Halahakoon, Alexander Kaltenboeck, Philip Cowen, Michael Browning, Sanjay G Manohar

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Psychopharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 14% of its field
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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 4 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
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

6 authors at 4 institutions in 2 countries.

Sheena K Au-YeungDepartment of Psychiatry, University of Oxford, Oxford, OX3 7JX, UK. sauyeung1@sheffield.ac.uk.ORCID http://orcid.org/0000-0002-0516-4755
Don Chamith HalahakoonDepartment of Psychiatry, University of Oxford, Oxford, OX3 7JX, UK.
Alexander KaltenboeckDepartment of Psychiatry, University of Oxford, Oxford, OX3 7JX, UK.
Philip CowenDepartment of Psychiatry, University of Oxford, Oxford, OX3 7JX, UK.
Michael Browning *Department of Psychiatry, University of Oxford, Oxford, OX3 7JX, UK.
Sanjay G Manohar *Nuffield Department of Clinical Neurosciences, John Radcliffe Hospital, University of Oxford, Level 6 West Wing, Oxford, OX3 9DU, UK.
Oxford Health NHS Foundation Trust · GBUniversity of Oxford · GBJohn Radcliffe Hospital · GBVienna General Hospital · AT

Funding

National Institute for Health and Care Research National Institute for Health and Care Research
6 · The paper itself

Abstract

Motivation allows us to energise actions when we expect reward and is reduced in depression. This effect, termed motivational vigour, has been proposed to rely on central dopamine, with dopaminergic agents showing promise in the treatment of depression. This suggests that dopaminergic agents might act to reduce depression by increasing the effects of reward or by helping energise actions. The aim of the current study was to investigate whether the dopamine agonist pramipexole enhanced motivational vigour during a rewarded saccade task. In addition, we asked whether the effects of pramipexole on vigour differ between reward contingent on performance and guaranteed reward. Healthy adult participants were randomised to receive either pramipexole (n = 19) or placebo (controls n = 18) for 18 days. The vigour of saccades was measured twice, once before the administration of study medication (Time 1) and after taking it for 12-15 days (Time 2). To separate motivation by contingency vs. reward, saccadic vigour was separately measured when (1) rewards were contingent on performance (2) delivered randomly with matched frequency, (3) when reward was guaranteed, (4) when reward was not present at all. Motivation increased response vigour, as expected. Relative to placebo, pramipexole also increased response vigour. However, there was no interaction, meaning that the effects of reward were not modulated by drug, and there was no differential drug effect on contingent vs. guaranteed rewards. The effect of pramipexole on vigour could not be explained by a speed/accuracy trade-off, nor by autonomic arousal as indexed by pupillary dilation. Chronic D2 stimulation increases general vigour, energising movements in healthy adults irrespective of extrinsic reward.

Indexed as

Dopamine AgonistsMotivationPramipexoleRewardSaccadesAdultBenzothiazolesDouble-Blind MethodFemaleHumansMalePsychomotor PerformanceYoung AdultBenzothiazolesDopamine AgonistsPramipexoleDopamineEye movementEye trackingMotivationPramipexoleRewardSaccadeVigour

Identifiers

PMID38494550
PMCPMC11199222
OpenAlexW4394738332

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.