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Eye movement desensitisation and reprocessing for post-traumatic stress in survivors of critical illness (EMERALD): a mixed-methods, randomised, single-blind, parallel group-controlled, feasibility trial.

Bates A, Cusack R, Golding H, Moyses H, Southam H, Rushbrook S, Highfield J, Pattison N, Baldwin DS, Grocott MPW. · EClinicalMedicine · 2026 · Single-blind randomized feasibility trial

Original publication · Original publication · Original publication

Recorded summary

The 40-person EMERALD trial in critical-illness survivors achieved 98% clinician-rated follow-up at 12 months. Exploratory PTSD symptom change favoured EMDR plus usual care by 14.1 points, with a 95% confidence interval of 6.2 to 22.0 points.

Recorded limitations

Feasibility, acceptability and safety were the primary objectives. The symptom estimate is hypothesis-generating and does not establish definitive treatment effectiveness.

Evidence and provenance

Chapter Trust Factor uses a minimum of three distinct qualifying studies. Publication records retain their own evidence and assessment.

Study design and assessment
design
Single-blind randomized feasibility trial
assessment
category
peer-reviewed
peer Reviewed
true
basis
Reported design checked against the primary publication abstract. Blinding terminology reflects the source report, not an independent risk-of-bias rating.
sources

https://pubmed.ncbi.nlm.nih.gov/42518933/ · https://doi.org/10.1016/j.eclinm.2026.104082 · https://pmc.ncbi.nlm.nih.gov/articles/PMC13382324/

assessed At
2026-10-26
registered Masking Basis
false
trust Factor
score
2
scope
Paper
status
assessed
randomized Controlled Trial
true
blinding
single
peer Reviewed
true
basis
Reported design checked against the primary publication abstract. Blinding terminology reflects the source report, not an independent risk-of-bias rating.
sources

https://pubmed.ncbi.nlm.nih.gov/42518933/ · https://doi.org/10.1016/j.eclinm.2026.104082 · https://pmc.ncbi.nlm.nih.gov/articles/PMC13382324/

review Scope
Existing publication-specific assessments and bibliographic indexing; no blanket full-text appraisal.
assessed At
2026-10-27
jadad
status
unassessed
score
Not recorded
evidence
intervention
Therapist-delivered EMDR
comparator
Treatment as usual
evidence Type
Clinical or experimental outcomes
source URLs

https://pubmed.ncbi.nlm.nih.gov/42518933/ · https://doi.org/10.1016/j.eclinm.2026.104082 · https://pmc.ncbi.nlm.nih.gov/articles/PMC13382324/

checked At
2026-10-26
review Scope
Primary publication abstract and bibliographic identity checked; comprehensive full-text risk-of-bias and Jadad assessment pending.
discovery Sources

https://daytab.com/study/t73vb9kv · https://europepmc.org/article/MED/42518933

selection Policy
Success-focused discovery selection, with material limitations retained; not an exhaustive systematic review.
trial Id
NCT05591625
Topics and recorded topic scores
  1. key
    vision:i
    title
    EMDR for PTSD and related mental-health outcomes
    collection
    vision
    trust Score
    2
Citation snapshot and identifiers
id
pmid-42518933
doi
10.1016/j.eclinm.2026.104082
pmid
42518933
citation Snapshot
count
1
source
Europe PMC
retrieved At
2026-10-26
url
https://europepmc.org/article/MED/42518933
citations By Collection
vision
1
Complete approved library record
id
pmid-42518933
publication Key
doi:10.1016/j.eclinm.2026.104082
aliases
None recorded
title
Eye movement desensitisation and reprocessing for post-traumatic stress in survivors of critical illness (EMERALD): a mixed-methods, randomised, single-blind, parallel group-controlled, feasibility trial.
journal
EClinicalMedicine
neurotransmitters
None recorded
year
2026
authors
Bates A, Cusack R, Golding H, Moyses H, Southam H, Rushbrook S, Highfield J, Pattison N, Baldwin DS, Grocott MPW.
design
Single-blind randomized feasibility trial
identity Conflict
Not recorded
doi
10.1016/j.eclinm.2026.104082
pmid
42518933
urls

https://pubmed.ncbi.nlm.nih.gov/42518933/ · https://doi.org/10.1016/j.eclinm.2026.104082 · https://pmc.ncbi.nlm.nih.gov/articles/PMC13382324/

collections

vision

categories

Clinical & self-report

targets
None recorded
priority
1
quotes
None recorded
summary
The 40-person EMERALD trial in critical-illness survivors achieved 98% clinician-rated follow-up at 12 months. Exploratory PTSD symptom change favoured EMDR plus usual care by 14.1 points, with a 95% confidence interval of 6.2 to 22.0 points.
limitation
Feasibility, acceptability and safety were the primary objectives. The symptom estimate is hypothesis-generating and does not establish definitive treatment effectiveness.
citation Count
1
citation Snapshot
count
1
source
Europe PMC
retrieved At
2026-10-26
url
https://europepmc.org/article/MED/42518933
study Design Assessment
category
peer-reviewed
peer Reviewed
true
basis
Reported design checked against the primary publication abstract. Blinding terminology reflects the source report, not an independent risk-of-bias rating.
sources

https://pubmed.ncbi.nlm.nih.gov/42518933/ · https://doi.org/10.1016/j.eclinm.2026.104082 · https://pmc.ncbi.nlm.nih.gov/articles/PMC13382324/

assessed At
2026-10-26
registered Masking Basis
false
paper Trust Assessment
score
2
scope
Paper
status
assessed
randomized Controlled Trial
true
blinding
single
peer Reviewed
true
basis
Reported design checked against the primary publication abstract. Blinding terminology reflects the source report, not an independent risk-of-bias rating.
sources

https://pubmed.ncbi.nlm.nih.gov/42518933/ · https://doi.org/10.1016/j.eclinm.2026.104082 · https://pmc.ncbi.nlm.nih.gov/articles/PMC13382324/

review Scope
Existing publication-specific assessments and bibliographic indexing; no blanket full-text appraisal.
assessed At
2026-10-27
citations By Collection
vision
1
topics
  1. key
    vision:i
    title
    EMDR for PTSD and related mental-health outcomes
    collection
    vision
    trust Score
    2
journal Key
eclinicalmedicine
journal Label
EClinicalMedicine
chapter Entries
  1. title
    Eye movement desensitisation and reprocessing for post-traumatic stress in survivors of critical illness (EMERALD): a mixed-methods, randomised, single-blind, parallel group-controlled, feasibility trial.
    journal
    EClinicalMedicine
    year
    2026
    authors
    Bates A, Cusack R, Golding H, Moyses H, Southam H, Rushbrook S, Highfield J, Pattison N, Baldwin DS, Grocott MPW.
    design
    Single-blind randomized feasibility trial
    urls

    https://pubmed.ncbi.nlm.nih.gov/42518933/ · https://doi.org/10.1016/j.eclinm.2026.104082 · https://pmc.ncbi.nlm.nih.gov/articles/PMC13382324/

    doi
    10.1016/j.eclinm.2026.104082
    pmid
    42518933
    targets
    None recorded
    categories

    Clinical & self-report

    citation Count
    1
    citation Snapshot
    count
    1
    source
    Europe PMC
    retrieved At
    2026-10-26
    url
    https://europepmc.org/article/MED/42518933
    study Design Assessment
    category
    peer-reviewed
    peer Reviewed
    true
    basis
    Reported design checked against the primary publication abstract. Blinding terminology reflects the source report, not an independent risk-of-bias rating.
    sources

    https://pubmed.ncbi.nlm.nih.gov/42518933/ · https://doi.org/10.1016/j.eclinm.2026.104082 · https://pmc.ncbi.nlm.nih.gov/articles/PMC13382324/

    assessed At
    2026-10-26
    registered Masking Basis
    false
    evidence
    intervention
    Therapist-delivered EMDR
    comparator
    Treatment as usual
    evidence Type
    Clinical or experimental outcomes
    source URLs

    https://pubmed.ncbi.nlm.nih.gov/42518933/ · https://doi.org/10.1016/j.eclinm.2026.104082 · https://pmc.ncbi.nlm.nih.gov/articles/PMC13382324/

    checked At
    2026-10-26
    review Scope
    Primary publication abstract and bibliographic identity checked; comprehensive full-text risk-of-bias and Jadad assessment pending.
    discovery Sources

    https://daytab.com/study/t73vb9kv · https://europepmc.org/article/MED/42518933

    selection Policy
    Success-focused discovery selection, with material limitations retained; not an exhaustive systematic review.
    trial Id
    NCT05591625
    id
    vision-i-pmid-42518933
    record Id
    pmid-42518933
    quotes
    None recorded
    source Pages
    None recorded
    summary
    The 40-person EMERALD trial in critical-illness survivors achieved 98% clinician-rated follow-up at 12 months. Exploratory PTSD symptom change favoured EMDR plus usual care by 14.1 points, with a 95% confidence interval of 6.2 to 22.0 points.
    limitation
    Feasibility, acceptability and safety were the primary objectives. The symptom estimate is hypothesis-generating and does not establish definitive treatment effectiveness.
    paper Trust Assessment
    score
    2
    scope
    Paper
    status
    assessed
    randomized Controlled Trial
    true
    blinding
    single
    peer Reviewed
    true
    basis
    Reported design checked against the primary publication abstract. Blinding terminology reflects the source report, not an independent risk-of-bias rating.
    sources

    https://pubmed.ncbi.nlm.nih.gov/42518933/ · https://doi.org/10.1016/j.eclinm.2026.104082 · https://pmc.ncbi.nlm.nih.gov/articles/PMC13382324/

    review Scope
    Existing publication-specific assessments and bibliographic indexing; no blanket full-text appraisal.
    assessed At
    2026-10-27
    publication Key
    doi:10.1016/j.eclinm.2026.104082
    collection
    vision
    chapter Number
    1
    topic Id
    i
    topic Title
    EMDR for PTSD and related mental-health outcomes
    trust Score
    2
evidence
intervention
Therapist-delivered EMDR
comparator
Treatment as usual
evidence Type
Clinical or experimental outcomes
source URLs

https://pubmed.ncbi.nlm.nih.gov/42518933/ · https://doi.org/10.1016/j.eclinm.2026.104082 · https://pmc.ncbi.nlm.nih.gov/articles/PMC13382324/

checked At
2026-10-26
review Scope
Primary publication abstract and bibliographic identity checked; comprehensive full-text risk-of-bias and Jadad assessment pending.
discovery Sources

https://daytab.com/study/t73vb9kv · https://europepmc.org/article/MED/42518933

selection Policy
Success-focused discovery selection, with material limitations retained; not an exhaustive systematic review.
trial Id
NCT05591625
jadad
status
unassessed
score
Not recorded
condition Evidence
  1. id
    ptsd
    evidence
    1. field
      curated primary-source summary
      text
      The 40-person EMERALD trial in critical-illness survivors achieved 98% clinician-rated follow-up at 12 months. Exploratory PTSD symptom change favoured EMDR plus usual care by 14.1 points, with a 95% confidence interval of 6.2 to 22.0 points.
      matched Text
      ptsd
conditions

ptsd

topic Trust Scores

2

full Text
status
not-indexed
retrieval Available
false

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