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Online CBT Intervention for Students With Adjustment Disorder

NCT05768308, Not applicable, Unknown, University of Warsaw

Trial 10

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

FieldValueSource
TitleOnline CBT Intervention for Students With Adjustment DisorderClinicalTrials.gov
NCT numberNCT05768308ClinicalTrials.gov
StatusUnknownClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment216 participants, estimatedClinicalTrials.gov
Lead sponsorUniversity of WarsawClinicalTrials.gov
ConditionsAdjustment DisordersClinicalTrials.gov
InterventionsInternet CBT-UP intervention iCBT-UP, Internet Progressive Muscle Realxation Training (iPMR)ClinicalTrials.gov
First posted2023-03-14ClinicalTrials.gov
Last updated2023-03-21ClinicalTrials.gov

Registered outcomes 20

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

ListOutcomeTime frameDescriptionSource
PrimaryChange in Adjustment disordermeasured at baseline, immediately after the interventions and 1 month follow upAdjustment disorder - The Adjustment Disorder New Module 20 (ADNM-20)ClinicalTrials.gov
SecondaryChange in Depressionmeasured at baseline, immediately after the interventions and 1 month follow upThe patient health questionnaire-9 (PHQ-9)ClinicalTrials.gov
SecondaryChange in General Anxiety Disordermeasured at baseline, immediately after the interventions and 1 month follow upGeneral Anxiety Disorder-7 (GAD-7)ClinicalTrials.gov
SecondaryChange in Stressmeasured at baseline, immediately after the interventions and 1 month follow upScale of experienced stress (PSS-10)ClinicalTrials.gov
SecondaryChange in Satisfaction with lifemeasured at baseline, immediately after the interventions and 1 month follow upSatisfaction with life scale (SWLS)ClinicalTrials.gov
SecondaryChange in Academic Adjustmentmeasured at baseline, immediately after the interventions and 1 month follow upAcademic adjustment scale (AAS)ClinicalTrials.gov
SecondaryChange in Experiential Avoidancemeasured at baseline, immediately after the interventions and 1 month follow upAcceptance and Action QuestionnaireClinicalTrials.gov
SecondaryChange in Cognitive Fusionmeasured at baseline, immediately after the interventions and 1 month follow upCognitive Fusion Questionnaire (CFQ)ClinicalTrials.gov
SecondaryChange in Self-compassionmeasured at baseline, immediately after the interventions and 1 month follow upSelf Compassion Scale - Short Form (SCS-SF)ClinicalTrials.gov
SecondaryChange in Mindfulnessmeasured at baseline, immediately after the interventions and 1 month follow upFive Facet Mindfulness Questionnaire (FFMQ-15)ClinicalTrials.gov
SecondaryChange in Persevative thinkingmeasured at baseline, immediately after the interventions and 1 month follow upPerseverative Thinking Questionnaire (PTQ)ClinicalTrials.gov
SecondaryChange in Mental well-beingmeasured at baseline, immediately after the interventions and 1 month follow upWarwick-Edinburgh Mental Well-being Scale (WEMWBS)ClinicalTrials.gov
SecondaryChange in Cognitive functioningmeasured at baseline, immediately after the interventions and 1 month follow upStroop Task (color-word)ClinicalTrials.gov
SecondaryChange in Academic performancemeasured at baseline, immediately after the interventions and 1 month follow upThis index will be based on a three recently received grades. The mean will be assessed.ClinicalTrials.gov
SecondaryChange in Daily Depressogenic adjustment7 days during the first week of the intervention and 7 days during the sixth week of the intervention timeMeasured in daily diaries. It will be measured by three items based on Becks triad.ClinicalTrials.gov
SecondaryChange in Daily negative thinking7 days during the first week of the intervention and 7 days during the sixth week of the intervention timeMeasured in daily diaries. Rumination and worrying. Daily worry measures will be measured with three items taken from Meyer et al. (1990).ClinicalTrials.gov
SecondaryChange in Emotional regulation7 days during the first week of the intervention and 7 days during the sixth week of the intervention timeMeasured in daily diaries. cognitive restructuring and emotional supression. This variables will be measured using one item (each scale) from Emotional Regulation Questionnaire (ERQ).ClinicalTrials.gov
SecondaryChange in Self-compassion7 days during the first week of the intervention and 7 days during the sixth week of the intervention timeMeasured in daily diaries, by three items from Self Compassion Scale (SCS).ClinicalTrials.gov
SecondaryChange in Daily-affect7 days during the first week of the intervention and 7 days during the sixth week of the intervention timeMeasured in daily diaries, based on circumplex model.ClinicalTrials.gov
SecondaryChange in Procrastination7 days during the first week of the intervention and 7 days during the sixth week of the intervention timeMeasured in daily diaries, by three items from The Pure Procrastination scale.ClinicalTrials.gov

Outcomes 0

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

TypeOutcomeTime framePopulationUnitsMeasured asSource

Results by group 0

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

OutcomeGroupCategoryValueSpreadUnitsSource

Participant flow 0

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

PeriodMilestoneGroupParticipantsUnits countedSource

Adverse events 0

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

TypeEventOrgan systemGroupAffectedAt riskEventsSource

Adverse event totals 0

The totals the trial posted for each group.

TotalGroupAffectedAt riskSource

Papers 1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
38041148DERIVEDPubMed

Grants 0

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.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal yearsSource

Trial comparisons 0

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

ComparisonSource

Tests 1

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

TestNamed asSource
Stroop Color-Word TestSecondary outcomeConductCognition

Source 5

FieldValueSource
Releasetrials-2026-11-12-0.4.0ClinicalTrials.gov
Release manifest SHA-2560f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4ClinicalTrials.gov
Registry capture2026-11-12ClinicalTrials.gov
Results copy, AACT2026-03-23ClinicalTrials.gov
NIH clinical studies file2026-11-13ClinicalTrials.gov

The same record as JSON

Release trials-2026-11-12-0.4.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)