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A Study on the Use of Healthcare Resources and Costs of Attention Deficit Hyperactivity Disorder (ADHD) in Adults in England

Healthcare Resources Utilization and Associated Costs of Adult ADHD in England

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05137704
Enrollment
2236
Registered
2021-11-30
Start date
2021-12-01
Completion date
2022-03-31
Last updated
2022-07-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Attention Deficit Hyperactivity Disorder (ADHD)

Brief summary

The main aim of the study is to learn about the demographic and clinical characteristics, healthcare resources utilization (HCRU) and costs associated with before and after ADHD diagnosis in England. No study medicines will be provided to participants in this study. The record available in Clinical Practice Research Datalink (CPRD) database and Hospital Episode Statistics (HES) database for ADHD participants will be assessed.

Interventions

OTHERNo intervention

This is a non-interventional study.

Sponsors

Takeda
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Age greater than or equal to (\>=) 18 years at the beginning of the patient observation period (that is 18-months prior to the adult ADHD diagnosis to ensure they would have been seen in adult health care services). 2. First record of an adult ADHD diagnosis between 01st January 2016 and 30th June 2018. 3. Data availability in the database at least during the 18-months before and after the index date.

Exclusion criteria

A participant will be excluded from the study if their CPRD linked to HES electronic medical record data includes: 1. Incomplete information for key demographics (that is, missing age or sex). 2. Clinical history of a diagnosis of ADHD during childhood or adolescence. 3. Prescription of a licensed adult ADHD medication (that is, methylphenidate, lisdexamfetamine, dexamfetamine, atomoxetine) during the pre-index period.

Design outcomes

Primary

MeasureTime frameDescription
Number of General Practitioner (GP) AppointmentsUp to approximately 36 monthsNumber of GP appointments will be reported.
Number of Referrals to PsychiatristUp to approximately 36 monthsNumber of referrals to psychiatrist will be reported.
Number of Referrals by SpecialistUp to approximately 36 monthsNumber of referrals by specialist will be reported.
Number of Outpatient Visits by SpecialistUp to approximately 36 monthsNumber of outpatient visits by specialist will be reported.
Number of Investigations UndergoneUp to approximately 36 monthsNumber and type of investigations undergone will be reported.
Number of Accident and Emergency VisitsUp to approximately 36 monthsNumber of accident and emergency visits will be reported.
Number of Reasons for AdmissionUp to approximately 36 monthsNumber of reasons for admission will be reported.
Number of Inpatient HospitalizationsUp to approximately 36 monthsNumber of inpatient hospitalizations will be reported.
Length of Stay in HospitalUp to approximately 36 monthsLength of stay in hospital will be reported.
Total Healthcare CostsUp to approximately 36 monthsHealth care cost includes prescription costs, primary health care consultations, investigations, hospital admissions, and outpatient appointments.
Number of Participants Prescribed With Pharmacological TreatmentsUp to approximately 36 monthsNumber of participants prescribed with pharmacological treatment will be reported.
Number of Participants Received Non-Pharmacological TreatmentsUp to approximately 36 monthsThe number of participants who received non-pharmacological treatments will be reported.
Number of Participants Received Non-Pharmacological TherapyUp to approximately 36 monthsThe non-pharmacological therapy will be cognitive behavioural therapy. Number of participants who received non-pharmacological therapy will be reported.

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026