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21. Guidelines and recommendations for ADHD in children and adolescents

disorders AGREE Appraisal of Guidelines for Research & Evaluation AMP amphetamines CADDRA Canadian ADHD Resource Alliance CADTH Canadian Agency for Drugs and Technologies in Health CPP clinical practice points CPS Canadian Paediatric Society DEX dextroamphetamine DSM Diagnostic and Statistical Manual of Mental Disorders ER extended release (also XR) IR immediate release LA long-acting MPH methylphenidate MR modified release NCCMH National Collaborating Centre for Mental Health NHMRC National Health (...) the current clinical evidence and findings of guidelines and recommendations. The report was also designed to explore the current utilization patterns and costs associated with the use of LA and SA ADHD medications. The information in this report is intended to help health care decision-makers, patients, health care professionals, health systems leaders, and policy-makers make informed decisions. 4 METHODS 4.1 Guidelines and Recommendations A limited literature search was conducted on key resources

2012 CPG Infobase

22. Treatment Patterns, Health Care Resource Utilization, and Health Care Cost Associated with Atypical Antipsychotics or Guanfacine Extended Release in Children and Adolescents with Attention-Deficit/Hyperactivity Disorder in Quebec, Canada. (PubMed)

Treatment Patterns, Health Care Resource Utilization, and Health Care Cost Associated with Atypical Antipsychotics or Guanfacine Extended Release in Children and Adolescents with Attention-Deficit/Hyperactivity Disorder in Quebec, Canada. Objective: To assess treatment patterns, health care resource utilization, and health care costs associated with use of atypical antipsychotics (AAPs) or the nonstimulant guanfacine extended release (GXR) after stimulant therapy for attention-deficit (...) /hyperactivity disorder (ADHD). In Canada, GXR is approved as a monotherapy for children and adolescents with ADHD or as an adjunct to stimulants, and AAPs are commonly used off-label as an adjunct to stimulants. Methods: Health care claims data (January 1, 2007 to March 31, 2016) from Quebec's provincial health plan were assessed for individuals with ADHD, 6-17 years of age, who received ≥1 stimulant followed by a first AAP or GXR prescription (index medication), without a diagnosis for which AAPs

2019 Journal of Child and Adolescent Psychopharmacology

23. 'Shine bright like a diamond!': is research on high-functioning ADHD at last entering the mainstream? (PubMed)

'Shine bright like a diamond!': is research on high-functioning ADHD at last entering the mainstream? The paper by Greven and colleagues (this issue) is intensifying discussion how research on attention-deficit/hyperactivity disorder (ADHD) can be moved away from the deficit-focused view to a concept, which is oriented towards resources a patient might be able to recruit to function at a high-level despite impairments. To promote understanding of high-functioning (HF)-ADHD, more longitudinal

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2018 Journal of Child Psychology and Psychiatry

24. KP415 Open-Label Safety Study in Children (6-12 Years of Age) With ADHD

KP415 Open-Label Safety Study in Children (6-12 Years of Age) With ADHD KP415 Open-Label Safety Study in Children (6-12 Years of Age) With ADHD - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. KP415 Open (...) -Label Safety Study in Children (6-12 Years of Age) With ADHD The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT03460652 Recruitment Status : Recruiting First Posted : March 9, 2018 Last Update Posted : April 20, 2018 See

2018 Clinical Trials

25. Gut Microbiome and Serum Metabolome Alterations in ADHD Patients

Primary Completion Date : February 27, 2020 Estimated Study Completion Date : May 27, 2020 Resource links provided by the National Library of Medicine related topics: Groups and Cohorts Go to Group/Cohort ADHD-patients The children 3-15 years old with ADHD. Diagnoses of the children with ADHD were made in Xijing Hospital according to criteria described in the Diagnostic and Statistical Manual of Mental Disorders (DSM-IV). Children with ADHD had an IQ score above 70. Controls-healthy children Age (...) Gut Microbiome and Serum Metabolome Alterations in ADHD Patients Gut Microbiome and Serum Metabolome Alterations in ADHD Patients - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Gut Microbiome and Serum

2018 Clinical Trials

26. Acoustic and Vestibular Noise as Possible Non-pharmacological Treatment of ADHD in School Children

Acoustic and Vestibular Noise as Possible Non-pharmacological Treatment of ADHD in School Children Acoustic and Vestibular Noise as Possible Non-pharmacological Treatment of ADHD in School Children - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove (...) one or more studies before adding more. Acoustic and Vestibular Noise as Possible Non-pharmacological Treatment of ADHD in School Children The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT03425669 Recruitment Status

2018 Clinical Trials

27. Added Value of the Oculomotor and Cognitive Examination in the Management of Patients With ADHD

Completion Date : December 31, 2019 Estimated Study Completion Date : December 31, 2019 Resource links provided by the National Library of Medicine related topics: available for: Arms and Interventions Go to Arm Intervention/treatment Experimental: ADHD patients 90 patients will be enrolled and assessed (i.e., neurocognitive and oculomotor tests) at baseline ; after a single low dose of methylphenidate (10 mg orally); and after 6 months of adequate dose of methylphenidate oral tablet Drug (...) Added Value of the Oculomotor and Cognitive Examination in the Management of Patients With ADHD Added Value of the Oculomotor and Cognitive Examination in the Management of Patients With ADHD - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one

2018 Clinical Trials

28. Increased Risk of ADHD Among Children With Bilateral Congenital Cataracts

Increased Risk of ADHD Among Children With Bilateral Congenital Cataracts Increased Risk of ADHD Among Children With Bilateral Congenital Cataracts - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Increased (...) Risk of ADHD Among Children With Bilateral Congenital Cataracts The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT03692728 Recruitment Status : Completed First Posted : October 2, 2018 Last Update Posted : October 4, 2018 Sponsor: Sun Yat-sen University Information provided by (Responsible Party

2018 Clinical Trials

29. Effects of multisensory stimuli on inhibitory control in adolescent ADHD: It is the content of information that matters (PubMed)

. These effects were reflected by modulations at the response selection stage (P3 ERP) in the medial frontal gyrus (BA32), but not at the attentional selection (P1, N1 ERPs) or resource allocation level (P2 ERP). Conflicting information during RI exerts its influences in adolescent ADHD via response selection mechanisms, but not via attentional selection. It is not the mere presence of concurrent information, but the presence of conflicting information during RI that may destabilize goal shielding processes (...) Effects of multisensory stimuli on inhibitory control in adolescent ADHD: It is the content of information that matters Even though deficits in inhibitory control and conflict monitoring are well-known in ADHD, factors that further modulate these functions remain to be elucidated. One factor that may be of considerable importance is how inhibitory control is modulated by multisensory information processing. We examined the influence of concurrent auditory conflicting or redundant information

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2018 NeuroImage : Clinical

30. ADHD/Me Bibliotherapy Study

of Bibliotherapy on Parent and Child Knowledge of ADHD and Treatment Follow-up Actual Study Start Date : August 20, 2018 Estimated Primary Completion Date : June 30, 2019 Estimated Study Completion Date : June 30, 2019 Resource links provided by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment Experimental: ADH-Me Book Families in both conditions will be told that they are receiving additional reading materials to help them and their child better (...) ADHD/Me Bibliotherapy Study ADHD/Me Bibliotherapy Study - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. ADHD/Me Bibliotherapy Study The safety and scientific validity of this study is the responsibility

2018 Clinical Trials

31. PART B: Efficacy and Safety of AEVI-001 in Children and Adolescents With ADHD and Without mGluR Mutations

PART B: Efficacy and Safety of AEVI-001 in Children and Adolescents With ADHD and Without mGluR Mutations PART B: Efficacy and Safety of AEVI-001 in Children and Adolescents With ADHD and Without mGluR Mutations - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100 (...) ). Please remove one or more studies before adding more. PART B: Efficacy and Safety of AEVI-001 in Children and Adolescents With ADHD and Without mGluR Mutations The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT03609619 Recruitment Status : Completed First Posted : August 1, 2018 Last Update Posted

2018 Clinical Trials

32. A 6-week Study to Evaluate the Safety and Efficacy of Methylphenidate HCl ERCT in 4-5 Year Old Children With ADHD

(Hcl) Extended Release Chewable Tablet (Erct) In 4-5 Year Old Children With Attention Deficit Hyperactivity Disorder (Adhd) Estimated Study Start Date : September 19, 2018 Estimated Primary Completion Date : April 22, 2021 Estimated Study Completion Date : April 22, 2021 Resource links provided by the National Library of Medicine related topics: available for: Arms and Interventions Go to Arm Intervention/treatment Placebo Comparator: Placebo one chewable tablet once daily in morning. Drug: Placebo (...) A 6-week Study to Evaluate the Safety and Efficacy of Methylphenidate HCl ERCT in 4-5 Year Old Children With ADHD A 6-week Study to Evaluate the Safety and Efficacy of Methylphenidate HCl ERCT in 4-5 Year Old Children With ADHD - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved

2018 Clinical Trials

33. Effectiveness of Collaborative Tele-Mental Health Services for ADHD in Primary Care

children with ADHD Masking: None (Open Label) Primary Purpose: Health Services Research Official Title: Effectiveness of Collaborative Tele-Mental Health Services for ADHD in Primary Care: A Randomized Trial in Dubai (ECTSAP- Dubai Trial) Actual Study Start Date : June 7, 2018 Estimated Primary Completion Date : December 31, 2018 Estimated Study Completion Date : December 31, 2018 Resource links provided by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention (...) Effectiveness of Collaborative Tele-Mental Health Services for ADHD in Primary Care Effectiveness of Collaborative Tele-Mental Health Services for ADHD in Primary Care - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before

2018 Clinical Trials

34. Single-dose Potassium Supplementation in Patients With ADHD for Whom the Anesthetic Lidocaine is Ineffective

, 2018 Resource links provided by the National Library of Medicine related topics: available for: Arms and Interventions Go to Arm Intervention/treatment Active Comparator: Lidocaine-effective ADHD: Intervention Single-dose potassium gluconate oral capsule intervention for ADHD subjects for whom lidocaine is effective Drug: Potassium Gluconate Oral Capsule Each subject will receive a dose of ~8 mg/kg of potassium. We will be giving a maximum of 14 mEq in a single dose. Placebo Comparator: Lidocaine (...) Single-dose Potassium Supplementation in Patients With ADHD for Whom the Anesthetic Lidocaine is Ineffective Single-dose Potassium Supplementation in Patients With ADHD for Whom the Anesthetic Lidocaine is Ineffective - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies

2018 Clinical Trials

35. Descriptive Epidemiology of a Specialized Consultation on ADHD in Adults at the Strasbourg University Hospital

Descriptive Epidemiology of a Specialized Consultation on ADHD in Adults at the Strasbourg University Hospital Descriptive Epidemiology of a Specialized Consultation on ADHD in Adults at the Strasbourg University Hospital - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved (...) studies (100). Please remove one or more studies before adding more. Descriptive Epidemiology of a Specialized Consultation on ADHD in Adults at the Strasbourg University Hospital (Stras-TDA) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details

2018 Clinical Trials

36. Exploratory fMRI Study on the Treatment for Impulsive Aggression in Children With ADHD

Neuroimaging Study to Evaluate the Effect on Brain Activity of SPN-810 for Impulsive Aggression (IA) in Patients With Attention-Deficit/Hyperactivity Disorder (ADHD) in Conjunction With Standard ADHD Treatment Estimated Study Start Date : May 30, 2019 Estimated Primary Completion Date : December 31, 2019 Estimated Study Completion Date : December 31, 2019 Resource links provided by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment Experimental: Single (...) Exploratory fMRI Study on the Treatment for Impulsive Aggression in Children With ADHD Exploratory fMRI Study on the Treatment for Impulsive Aggression in Children With ADHD - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies

2018 Clinical Trials

37. Cognitive Rehabilitation (Mega Team) and Its Effects on Emotional and Behavioral Regulation in ADHD, ASD, and CHD

Cognitive Rehabilitation (Mega Team) and Its Effects on Emotional and Behavioral Regulation in ADHD, ASD, and CHD Cognitive Rehabilitation (Mega Team) and Its Effects on Emotional and Behavioral Regulation in ADHD, ASD, and CHD - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved (...) studies (100). Please remove one or more studies before adding more. Cognitive Rehabilitation (Mega Team) and Its Effects on Emotional and Behavioral Regulation in ADHD, ASD, and CHD The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov

2018 Clinical Trials

38. Adaptive Response to Intervention (RTI) for Students With ADHD

Intervention Model: Sequential Assignment Masking: None (Open Label) Primary Purpose: Treatment Official Title: Adaptive Response to Intervention (RTI) for Students With ADHD Actual Study Start Date : May 14, 2018 Estimated Primary Completion Date : June 2021 Estimated Study Completion Date : June 2021 Resource links provided by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment No Intervention: Business as Usual (BAU) One-third of participants (...) Adaptive Response to Intervention (RTI) for Students With ADHD Adaptive Response to Intervention (RTI) for Students With ADHD - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Adaptive Response

2018 Clinical Trials

39. Omega-3 Polyunsaturated Fatty Acids in Youth With ADHD

Omega-3 Polyunsaturated Fatty Acids in Youth With ADHD Omega-3 Polyunsaturated Fatty Acids in Youth With ADHD - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Omega-3 Polyunsaturated Fatty Acids in Youth (...) With ADHD The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT03542643 Recruitment Status : Completed First Posted : May 31, 2018 Last Update Posted : June 15, 2018 Sponsor: China Medical University Hospital Collaborators: National Science Council, Taiwan King's College London Information provided

2018 Clinical Trials

40. A 6-week Study to Evaluate the Safety and Efficacy of Quillichew ERCT in 4-5 Year Old Children With ADHD.

And Safety Of Quillichew (Methylphenidate Hydrochloride (Hcl)) Extended Release Chewable Tablets (Erct) In 4-5 Year Old Children With Attention Deficit Hyperactivity Disorder (Adhd) Estimated Study Start Date : October 31, 2018 Estimated Primary Completion Date : October 12, 2021 Estimated Study Completion Date : October 12, 2021 Resource links provided by the National Library of Medicine related topics: available for: Arms and Interventions Go to Arm Intervention/treatment Active Comparator: Quillichew (...) A 6-week Study to Evaluate the Safety and Efficacy of Quillichew ERCT in 4-5 Year Old Children With ADHD. A 6-week Study to Evaluate the Safety and Efficacy of Quillichew ERCT in 4-5 Year Old Children With ADHD. - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100

2018 Clinical Trials

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