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Trial · NCT04273685

Cognitive Remediation and Social Recovery in Early Psychosis

NCT04273685, Not applicable, Unknown, National University of Ireland, Galway, Ireland

3 sourcestrials-2026-11-12-0.4.0

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ConductScience Library. Cognitive Remediation and Social Recovery in Early Psychosis. Trials, record NCT04273685. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04273685

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Cognitive Remediation and Social Recovery in Early Psychosis
NCT number
NCT04273685
Status
Unknown
Phases
Not applicable
Enrollment
40 participants, estimated
Lead sponsor
National University of Ireland, Galway, Ireland
Conditions
Psychosis
Interventions
Cognitive remediation training, social recovery therapy, treatment as usual
First posted
2020-02-18
Last updated
2022-03-28

Source ClinicalTrials.gov

Registered outcomes14

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimarySocial and Occupational Functional Assessment Scale (SOFAS) (change from baseline)Post study at 12 weeks and follow up 3-5 months post study
The Social and Occupational Functional Assessment Scale is a global rating of current functioning ranging from 0 to 100.Lower scores represent lower functioning and higher scores represent higher functioning.For example a score of 100 represents superior functioning in a wide range of activities,a score of 50 represents serious impairment in social, occupational or school functioning, a score of 30 represents an inability to function in almost all areas of activity. The minimum value is 0 and the maximum value is 100.
SecondaryTime Use SurveyBaseline, post study at 12 weeks,follow up 3-5 months post study
The Time Use Survey is a semi-structured interview that enquires about time spent over the past month on work, education, voluntary work, leisure, sports, housework or chores, and child care. Time spent on each of the activities is calculated in terms of the average number of hours per week. The activities are summed to create two scores: constructive economic activity (work, education, voluntary work, housework or chores, and child care) and structured activity (constructive economic activity plus leisure and sports activities).A higher score indicates superior social functioning, a lower score represents impaired social functioning. Less than 45 hours of structured activity per week is considered a threshold for being at risk of social disability, less than 30 hours per week is threshold for social disability and indicative of poor social functioning, and less than 15 hours per week is considered to reflect serious social disability.
SecondaryCambridge Neuropsychological Test Automated Battery (CANTAB)- Emotion Recognition Task- change being assessed.Baseline, post study at 12 weeks and 3-5 months post study
This task measures the ability to identify six basic emotions in facial expressions along a continuum of expression magnitude. Computer-morphed images derived from the facial features of real individuals, each showing a specific emotion, are displayed on the screen, one at a time. Each face is displayed for 200ms and then immediately covered up to prevent residual processing of the image. The participant must select which emotion the face displayed from 6 options (sadness, happiness, fear, anger, disgust or surprise). The task takes 6 minutes to complete.
SecondaryThe Reading the mind in the eyes task- change being assessed.Baseline, post study at 12 weeks,follow up 3-5 months post study
This task measures the capacity to understand mental states of others from expressions in the eye region of the face. Participants view 36 photos and choose the most accurate descriptor word from four choices for the thought/feeling that was portrayed. As noted above, definitions of the response choices are embedded in the task. The dependent measure was the total number of correct responses, ranging from 0 to 36
SecondaryThe Hinting Task - change being assessed.Baseline, post study at 12 weeks,follow up 3-5 months post study
This task examines the ability to infer the true intent of indirect speech. Ten short passages presenting an interaction between two characters are read aloud. Each passage ends with one of the characters dropping a hint, and participants explain what the character truly meant. If the first response provided was inaccurate, a second hint is delivered, allowing participants to earn partial credit. Total scores range from 0 to 20
SecondaryThe Bell Lysaker Emotion Recognition Task (BLERT)- change being assessed.Baseline, post study at 12 weeks,follow up 3-5 months post study
This task measures recognition of seven emotional states: happiness, sadness, fear, disgust, surprise, anger, or no emotion. Participants identified the emotion shown in 21 videos of a male actor providing dynamic facial, vocal-tonal, and upper-body movement cues. Performance Is indexed as the total number of correctly identified emotions (ranging from 0 to 21).
SecondaryWechsler abbreviated scale of intelligence- similarities and matrix reasoning subtestsBaseline, post study at 12 weeks,follow up 3-5 months post study
The similarities and matrix reasoning subtests from the Wechsler Adult Scale of Intelligence 3rd edition (WAIS-III) is a brief, reliable measure of cognitive ability for use in clinical, educational and research settings. The similarities subtests scores range from 0 - 33 with higher scores indicating better verbal comprehension. Matrix reasoning subtest scores range from 0 - 26 with higher scores reflecting better perceptual organization. Once raw scores are derived they are converted to scaled scores adjusted for age.
SecondaryWechsler Memory scale 3rd edition- logical memory and letter number sequencing subtestsBaseline, post study at 12 weeks,follow up 3-5 months post study
The Wechsler Memory Scale 3rd edition, logical memory subtest is used to assess episodic and auditory memory in immediate and delayed conditions.Logical memory immediate scores range from 0-75, and delayed scores range from 0-50. The letter-number sequencing subtest from the Wechsler Memory Scale 3rd edition is used to assess working memory. Scores range from 0-21. Higher scores on the Wechsler Memory Scale 3rd edition subtests indicate better memory function. Raw scores are converted to scaled scores adjusted for age.
SecondaryRey Osterreith Complex Figure (ROCF)Baseline, post study at 12 weeks,follow up 3-5 months post study
The Rey Osterreith Complex Figure is an assessment which measures visual memory by asking the participant to reproduce a complicated line drawing, first by copying it freehand and then drawing from memory (immediate and delayed conditions). Scores range from 0-36 with higher scores indicating better visual memory.
SecondarySTROOPBaseline, post study at 12 weeks,follow up 3-5 months post study
The Stroop test measures a person's sustained attention for word reading and color naming with/without interference. A computerized Stroop task measures mean reaction times (RTs) for congruent and incongruent trials. Four colour words (green, red, yellow, and blue) written in congruent or incongruent colour are randomly presented on screen. The Stroop test detects attentional interference via the measurement of response latency (calculated as mean RT for incongruent trials minus mean RT for congruent trials) when participants are asked to inhibit word meaning and indicate the ink colour of the word. Longer latencies are interpreted as greater interference by word content and lower executive function.

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers15

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
16678388BACKGROUNDPubMed
18930378BACKGROUNDPubMed
19195844BACKGROUNDPubMed
20620163BACKGROUNDPubMed
21525166BACKGROUNDPubMed
23059624BACKGROUNDPubMed
23728248BACKGROUNDPubMed
25001267BACKGROUNDPubMed
26004421BACKGROUNDPubMed
28139356BACKGROUNDPubMed

1 to 10 of 15

See all 15 papers

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests6

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

TestNamed asSource
Emoji Emotion RecognitionSecondary outcomeConductCognition
Indirect Hints TaskSecondary outcomeConductCognition
Letter-Number Sequencing TaskSecondary outcomeConductCognition
Matrix ReasoningSecondary outcomeConductCognition
Short Story RecallSecondary outcomeConductCognition
Stroop Color-Word TestSecondary outcomeConductCognition

Source

Release
trials-2026-11-12-0.4.0
Release manifest SHA-256
0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4
Registry capture
2026-11-12
Results copy, AACT
2026-03-23
NIH clinical studies file
2026-11-13

Source ClinicalTrials.gov

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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GET https://conductscience.org/api/trials/v1/NCT04273685/registered