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NCT05039853: IMPREL

Improving Mental Health Following Early PREgnancy Loss Using a Brief Cognitive Task

Completed NA Last updated 29 November 2024
What this trial tests

NA trial testing Brief cognitive task-based intervention in Post-traumatic Stress Disorder in 168 participants. Completed in 1 June 2024.

Timeline
9 December 2021
Primary endpoint
21 March 2024
1 June 2024

Quick facts

Lead sponsorImperial College London
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposeprevention
Enrollment168
Start date9 December 2021
Primary completion21 March 2024
Estimated completion1 June 2024
Sites1 location across United Kingdom

Drugs / interventions tested

Conditions studied

Sponsor

Imperial College London

Who can join

18 and older, female only, with Post-traumatic Stress Disorder or Miscarriage. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a randomised controlled trial designed to investigate the impact of a brief-cognitive task based intervention on intrusive memories, mental health symptoms and daily functioning, in women following an early pregnancy loss.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Post-traumatic Stress Disorder

Currently open trials in the same condition.

Other Imperial College London trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05039853.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing