Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Class |
|---|---|
| Goethe University | OTHER |
| Semmelweis University | OTHER |
| University Medical Center Nijmegen | OTHER |
Not provided
Not provided
Not provided
Not provided
A multicentre randomized double-blind placebo controlled parallel design (10 weeks) study investigating probiotic supplementation in highly impulsive adults (18-65 yrs; N=180). The probiotic studied is Synbiotic2000Forte that contain three well-studied anti-inflammatory lactic acid bacteria (LABs) and four fermentable fibers: Pediococcus pentosaceus 5-33:3, Lactobacillus paracasei subsp paracasei 19, and Lactobacillus plantarum 2362 in combination with the following four fermentable fibres: betaglucan, inulin, pectin and resistant starch. With this study we aim to detect, whether treatment with probiotics is effective in adults with high levels of impulsivity, compulsivity, and aggression.
Impulsivity is a cross-disorder trait relevant in several psychiatric disorders, e.g. Attention Deficit Hyperactivity Disorder (ADHD) and Borderline Personality Disorder (BPD). They place a significant burden on patients, families and society in general. Only adults (aged 18 - 65 years) with a diagnosis of ADHD and/or BPD will be included in this study. We will also try to include at least 30% female participants to gender-balance the study.
Recruitment and treatment of participants will be provided at three trial centres: Vall d'Hebron Research Institute (VHIR), Goethe University Frankfurt (GU), Semmelweis University (SU), each enrolling 60 participants. Randomization to receive either Synbiotic2000Forte or placebo will be performed when signed informed assent by the participant has been obtained, eligibility checks have been conducted and at baseline assessment. An independent randomization service (www.randomization.com) will be used to ensure reliability and credibility in the randomization process. The study is double-blinded; neither the participants nor the clinicians involved in the study will have access to the randomization list.
In this placebo-controlled 10-week, we will evaluate a probiotic formula for oral administration called Synbiotic2000Forte (SF). Participants will take the probiotic once daily in the form of a powder that can be spread on top of cold foods such as muesli, salad, or yoghurt. Placebo will be a non-digestable carbohydrate with similar texture and flavor to the SF. Participants will be assessed at baseline before treatment is started (baseline demographics and primary- and secondary outcome measures will be collected and then monitored every five weeks for a total of 5 visits.
Proper conduct of data collection in the trial will be monitored by on-site visits of a monitoring staff throughout the study, and quality of data collected will further be monitored regularly by a statistical supervision team. Questionnaire data will be collected through Castor. All information collected in this study will remain strictly confidential. Data of participants will be coded in such a way that participants cannot be identified from the corresponding data according to the regulations (unique pseudocode identifier).
This study will be conducted according to the principles of the Declaration of Helsinki, version of 2008 and in accordance with the Medical Research Involving Human Subjects Act (WMO, as well as according to the ICH GCP Guideline E6 (1996), EU Directive 2001/20/EC and applicable regulatory requirements and guidelines in the participating countries/regions. Before the first subject has been enrolled in the trial, all ethical and legal requirements were met.
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Treatment with a probiotic | Experimental | Synbiotic2000Forte (SF) it is composed of 3 LAB species known to have anti-inflammatory effects and restoring the intestinal barrier, and 4 fermentable fibers: Pediococcus pentosaceus 5-33:3, Lactobacillus paracasei subsp paracasei 19, and Lactobacillus plantarum 2362 in combination with the following four fermentable fibres: betaglucan, inulin, pectin and resistant starch, a formula that is currently produced by Synbiotic AB, Sweden. |
|
| Treatment with placebo powder | Placebo Comparator | Placebo will be a non-digestable carbohydrate with similar texture and flavor to the SF also provided by Synbiotic AB, Sweden. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Treatment with a probiotic | Dietary Supplement | All participants will take the probiotic once daily for 10 weeks in the form of a powder that can be spread on top of cold foods such as muesli, salad, or yogurt. |
| Measure | Description | Time Frame |
|---|---|---|
| Change in the self-rating of affective reactivity (ARI-S) | Assessed at Baseline, at week 5, week 10 and week 11. | |
| Clinical Global Impression - Improvement (CGI-I) total score of 1 or 2 (much improved, very much improved). | assessed at weeks 5, 10, and 11. |
| Measure | Description | Time Frame |
|---|---|---|
| Change in Clinical Global Impression - Severity (CGI-S) | Screnning assessment and again at weeks 1, 5 and 10. | |
| Change in ADHD symptom severity total score | assessed by the Adult Attention-Deficit/Hyperactivity Disorder Rating Scale (ADHD-RS). The ADHD-RS is a 18-items scale self-report version for assessing symptoms for ADHD DSM-IV. It consists of a subscale of inattention (IN, 9-items), another of hyperactivity/impulsivity (H / I, 9-items) and the total (TOT, 18-items). The interviewees are asked about the frequency of the symptoms over the past 6 months. Each item is scored from 0 to 3 points, and the highest scores indicates more severe symptomatology of ADHD. |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Universitätsklinikum Frankfurt - Goethe Universität | Frankfurt | 60528 | Germany | |||
| Semmelweis University |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 38885746 | Derived | Arteaga-Henriquez G, Ramos-Sayalero C, Ibanez-Jimenez P, Karina Rosales-Ortiz S, Kilencz T, Schiweck C, Schnorr I, Siegl A, Arias-Vasquez A, Bitter I, Fadeuilhe C, Ferrer M, Lavebratt C, Matura S, Reif A, Rethelyi JM, Richarte V, Rommelse N, Antoni Ramos-Quiroga J. Efficacy of a synbiotic in the management of adults with Attention-Deficit and Hyperactivity Disorder and/or Borderline Personality Disorder and high levels of irritability: Results from a multicenter, randomized, placebo-controlled, "basket" trial. Brain Behav Immun. 2024 Aug;120:360-371. doi: 10.1016/j.bbi.2024.06.012. Epub 2024 Jun 15. | |
| 36375174 |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| ID | Term |
|---|---|
| D007175 | Impulsive Behavior |
| D003193 | Compulsive Personality Disorder |
| D001289 | Attention Deficit Disorder with Hyperactivity |
| D001883 | Borderline Personality Disorder |
| D000374 | Aggression |
| D001523 | Mental Disorders |
| ID | Term |
|---|---|
| D001519 | Behavior |
| D010554 | Personality Disorders |
| D019958 | Attention Deficit and Disruptive Behavior Disorders |
| D065886 | Neurodevelopmental Disorders |
Not provided
Not provided
| ID | Term |
|---|---|
| D013812 | Therapeutics |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Treatment with placebo | Other | All participants will take the placebo once daily for 10 weeks. |
|
| Baseline assessment and again at weeks 5, and 10. |
| Change in impulsive behaviour | assessed by the self-rated multi-dimensional impulsivity (UPPS-P) | Baseline assessment and again at weeks 5, and 10. |
| Change in Self/other rating of aggression and emotional lability (SDQ) | Baseline assessment and again at weeks 5, and 10. |
| Change in Clinician rating of compulsivity (Y-BOCS) | Baseline assessment and again at weeks 5, and 10. |
| Change in sleep problems | 5-item questionnaire. | Baseline assessment and again at weeks 5, and 10. |
| Change in the somatic complaints and side effects describe by the patient. | assessed at weeks 5, 10, and 11. |
| Change in body composition parameters | Change in weight in kilograms | Baseline assessment and again at weeks 5, and 10. |
| Changes in concentrations of blood biomarkers including hormones, neurotransmitters and nutrients. | Baseline assessment and again at weeks 5, and 10. |
| Change in microbiome composition | Baseline assessment and again at weeks 5, and 10. |
| Change in nutritional intake | Participants will be asked to complete at least three 24-h dietary recall (24HDR) per visit, including two week days and one weekend day (non-consecutive days). | Baseline assessment and again at weeks 5, and 10. |
| Treatment adherence | Probabilistic Medication Adherence Scale (ProMAS); The total score ranges from 0-18 with a higher score indicating better adherence. Each item is scored as yes (1) or No (0). | Baseline assessment and again at weeks 5, and 10. |
| Change in functioning problems | Functioning Assessment Short Test (FAST ) | Baseline assessment and again at weeks 5, and 10. |
| Self-rating of emotion regulation difficulties | assessed by Difficulties in Emotion Regulation Scale (DERS-16). The total score ranges from 16-80 with a higher score indicating higher difficulties in emotion regulation. Each item is scored as Almost never (1), Somtimes (2), About half the time (3), Most of the time (4), Almost always (5). | Baseline assessment and again at weeks 5, and 10. |
| Change in gastrointestinal symptoms | assessed by Bristol Stool Scale; There are seven types of stool in the Bristol Stool Scale:
| Baseline assessment and again at weeks 5, 10, and 11. |
| Change in physical activity: Duration of the activity | parameter measured with a movement sensor.The actigraphy records the duration of the activity. The activity report outcomes how long the participant move (days/hours/min). | Baseline assessment and at week 10. |
| Change in physical activity: Intensity of the activity | parameter measured with a movement sensor. The actigraphy records the intensity of the activity. The report of activity outcomes the intensity of the movement classified in four categories from lowest intensity to highest intensity; these categories are:
| Baseline assessment and at week 10. |
| Change in neurocognitive measure: Detectability | assessed by Conners' Continuous Performance Test II (CPTII). Assessment duration: 14min. Physicological parameter assessed: - Detectability (d'): this is a measure of how well the respondent discriminates non-targets (i.e. the letter X) from targets (i.e. all the other letters). This variable is also a signal detection statistic that measures the difference between the signal (targets) and noise (non-targets) distributions. On the Conners CPT-II, d' is reverse scored so that higher raw score and T-score values indicate worse performance (i.e. poorer discrimination) | Baseline assessment and again at weeks 5 and 10. |
| Change in neurocognitive measure: Omissions | assessed by Conners' Continuous Performance Test II (CPTII). Assessment duration: 14min. Physicological parameter assessed: - Omissions (%): Omissions are missed targets. High omissions error rates indicate that the respondent was not responding to the target stimuli due to a specific reason (e.g. difficulty focusing). Omission errors are generally an indicator of inattentiveness. | Baseline assessment and again at weeks 5 and 10. |
| Change in neurocognitive measure: Commissions | assessed by Conners' Continuous Performance Test II (CPTII). Assessment duration: 14min. Physicological parameter assessed: - Commissions (%): Commissions are incorrect responses to non-targets. Depending on the respondent's HRT, high commission error rates may indicate either inattentiveness or impulsivity. If high commission error rates are coupled with slow reaction times, then the respondent was likely inattentive to the stimulus type being presented and thus responded to a high rate of non-targets. If high commission error rates are combined with fast reaction times, the respondent was likely rushing to respond and failed to control his or her impulses when responding to the non-targets. In the latter case, high commission error rates would reflect impulsivity rather than inattentiveness. | Baseline assessment and again at weeks 5 and 10. |
| Change in neurocognitive measure: Perseverations | assessed by Conners' Continuous Performance Test II (CPTII). Assessment duration: 14min. Physicological parameter assessed: - Perseverations (%): Perseverations are responses that are made in less than 100 milliseconds following the presentation of a stimulus. Normal expectations of physiological ability to respond make it virtually impossible for a respondent to perceive and react to a stimulus so quickly. Perseverations are unusually either slow responses to a preceding stimulus, a random response, an anticipatory response, or a repeated response without consideration of the task requirements. Perseverations may be related to impulsivity or an extremely liberal response style. Perseverations are, therefore, likely the result of anticipatory, repetitive, or impulsive responding. | Baseline assessment and again at weeks 5 and 10. |
| Change in neurocognitive measure: Hit Reaction Time (HRT) | assessed by Conners' Continuous Performance Test II (CPTII). Assessment duration: 14min. Physicological parameter assessed: - Hit Reaction Time (HRT): HRT is the mean response speed, measured in milliseconds, for all non-perseverative responses made during the entire administration. An atypically slow HRT may indicate inattentiveness (especially when error rates are high), but it may also be the results of a very conservative response style. Alternatively, a very fast HRT, when combined with high commission error rates, may indicate impulsivity. | Baseline assessment and again at weeks 5 and 10. |
| Change in neurocognitive measure: Hit Reaction Time Standard Deviation (HRT SD) | assessed by Conners' Continuous Performance Test II (CPTII). Assessment duration: 14min. . Physicological parameter assessed: - Hit Reaction Time Standard Deviation (HRT SD): HRT SD measures the consistency of response speed to targets for the entire administration. A high HRT SD indicates greater inconsistency in response speed. Response speed inconsistency is sometimes indicative of an inattentiveness, suggesting that the respondent was less engaged and processed stimuli less efficiently during some parts of the administration. | Baseline assessment and again at weeks 5 and 10. |
| Change in neurocognitive measure: Variability | assessed by Conners' Continuous Performance Test II (CPTII). Assessment duration: 14min. Physicological parameter assessed: - Variability: Variability, like HRT SD, is a measure of response speed consistency, however, Variability is a "within respondent" measure (i.e. the amount of variability the respondent showed in 18 separate sub-blocks of the administration in relation to his or her overall HRT SD score). Although Variability is a different measure than HRT SD, the two measures typically produce comparable results and are both related to inattentiveness. High response speed variability indicates that the respondent's attention and processing efficiency varied throughout the administration. | Baseline assessment and again at weeks 5 and 10. |
| Change in self-rating of perceived stress. The total score ranges from 0-40 with a higher score indicating higher perceived stress. Each item is scored as Never (0), Almost never (1), Sometimes (2), Fairly Often (3), Very Often (4). | assessed by Perceived Stress Scale (PSS) | Baseline assessment and at week 10. |
| Budapest |
| 1082 |
| Hungary |
| Hospital Universitari Vall d'Hebron | Barcelona | 08035 | Spain |
| Derived |
| Stoffers-Winterling JM, Storebo OJ, Pereira Ribeiro J, Kongerslev MT, Vollm BA, Mattivi JT, Faltinsen E, Todorovac A, Jorgensen MS, Callesen HE, Sales CP, Schaug JP, Simonsen E, Lieb K. Pharmacological interventions for people with borderline personality disorder. Cochrane Database Syst Rev. 2022 Nov 14;11(11):CD012956. doi: 10.1002/14651858.CD012956.pub2. |
| 32046750 | Derived | Arteaga-Henriquez G, Rosales-Ortiz SK, Arias-Vasquez A, Bitter I, Ginsberg Y, Ibanez-Jimenez P, Kilencz T, Lavebratt C, Matura S, Reif A, Rethelyi J, Richarte V, Rommelse N, Siegl A, Ramos-Quiroga JA. Treating impulsivity with probiotics in adults (PROBIA): study protocol of a multicenter, double-blind, randomized, placebo-controlled trial. Trials. 2020 Feb 11;21(1):161. doi: 10.1186/s13063-019-4040-x. |
| D000096762 | Aberrant Motor Behavior in Dementia |
| D001526 | Behavioral Symptoms |
| D012919 | Social Behavior |