Emotional and Non-emotional Regulation in Patients With Emotional Instability and ADHD
NCT02797873, Not applicable, Unknown, Karolinska Institutet
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Emotional and Non-emotional Regulation in Patients With Emotional Instability and ADHD | ClinicalTrials.gov |
| NCT number | NCT02797873 | ClinicalTrials.gov |
| Status | Unknown | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 60 participants, estimated | ClinicalTrials.gov |
| Lead sponsor | Karolinska Institutet | ClinicalTrials.gov |
| Conditions | Emotional Instability Personality Disorder (Borderline Personality Disorder), Attention Deficit Hyperactivity Disorder, Healthy Controls | ClinicalTrials.gov |
| Interventions | fMRI - Stroop task, fMRI - MID task, Stop Signal Task, SCID-II, SDQ, ASRS, AQ, TAS-20, Raven's SPM, Reading ability, Ishihara's tests for colour deficiency, Additional questionnaire, Brown-ADD, MFQ, STAI-T, BIS, DAWBA, STAI-S, Sleepiness rating, Motivation rating, FEFA2, Structural T1 MRI scan, Structural T2 MRI scan, DTI MRI scan, Resting state MRI scan | ClinicalTrials.gov |
| First posted | 2016-06-14 | ClinicalTrials.gov |
| Last updated | 2016-06-14 | ClinicalTrials.gov |
Registered outcomes 19
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | fMRI BOLD signal differences between groups - in Stroop task | Acquired during fMRI scan | BOLD signal Neutral and Emotional blocks, and for Congruent and Incongruent trials (order dependent) | ClinicalTrials.gov |
| Primary | fMRI signal variations within patient group during Stroop task, depending on level of ADHD symptoms - in Stroop task | Acquired during fMRI scan | BOLD signal Neutral and Emotional blocks, and for Congruent and Incongruent trials (order dependent) | ClinicalTrials.gov |
| Primary | Reaction times in Stroop task | Acquired during fMRI scan | ClinicalTrials.gov | |
| Primary | fMRI BOLD signal differences between groups - in Monetary Incentive Delay task (MID) | Acquired during fMRI scan | BOLD signal during anticipation phase of different levels of reward, and BOLD signal during receipt/outcome phase of different levels of reward. | ClinicalTrials.gov |
| Primary | fMRI BOLD signal differences within patient group during MID task, depending on level of ADHD symptoms - in MID task | Acquired during fMRI scan | BOLD signal during anticipation phase of different levels of reward, and BOLD signal during receipt/outcome phase of different levels of reward. | ClinicalTrials.gov |
| Primary | Reaction times in MID task | Acquired during fMRI scan | ClinicalTrials.gov | |
| Primary | Stop Signal reaction times (SSRT) from Stop Signal Task (SST) | Data necessary for estimation of SSRT acquired during fMRI scan | ClinicalTrials.gov | |
| Secondary | Brown-ADD score | Acquired from questionnaire at first visit | ClinicalTrials.gov | |
| Secondary | Mood and Feelings questionnaire | Acquired from questionnaire at first visit | dimensional measurement of depressive symptoms | ClinicalTrials.gov |
| Secondary | STAI-T score | Acquired from questionnaire at first visit | Measuring anxiety trait level | ClinicalTrials.gov |
| Secondary | Barratt's impulsivity scale (BIS) | Acquired from questionnaire at first visit | ClinicalTrials.gov | |
| Secondary | STAI-S score | Baseline, acquired from questionnaire Day 2 | Measuring anxiety state level | ClinicalTrials.gov |
| Secondary | Sleepiness score | Acquired during MRI scan, on Day 2 | Acquired 6 times in MRI scanner as follows: 1) Before first Stroop session. 2) Between Stroop session 1 and 2. 3) After Stroop session 2. 4) Before first MID session. 5) Between MID session 1 and 2. 6) After MID session 2. | ClinicalTrials.gov |
| Secondary | Motivation score | Acquired during MRI scan, on Day 2 | Acquired 6 times in MRI scanner as follows: 1) Before first Stroop session. 2) Between Stroop session 1 and 2. 3) After Stroop session 2. 4) Before first MID session. 5) Between MID session 1 and 2. 6) After MID session 2. | ClinicalTrials.gov |
| Secondary | Structural MRI data - volume | Acquired during MRI scan | ClinicalTrials.gov | |
| Secondary | Structural MRI data - surface area | Acquired during MRI scan | ClinicalTrials.gov | |
| Secondary | Structural MRI data - thickness | Acquired during MRI scan | ClinicalTrials.gov | |
| Secondary | Functional Connectivity (FC) | Acquired during resting state MRI scan | Measuring the FC value between ROIs defined in hypothesis to determine strength of connectivity between these different brain regions. | ClinicalTrials.gov |
| Secondary | Fractional Anisotropy (FA) of white matter | Acquired during Diffusion Tensor Imaging (DTI) scan | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 0
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|
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.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 3
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|---|---|
| Monetary Incentive Delay | Primary outcome | ConductCognition |
| Stop-Signal Task | Primary outcome | ConductCognition |
| Stroop Color-Word Test | Primary outcome | ConductCognition |
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
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)