High Intensity Training for Adults With ADHD in Specialised Mental Health Care
HITADHD
High-intensity Training for Adults With ADHD in Specialised Mental Health Care: A Mixed Methods Feasibility Study
1 other identifier
interventional
30
1 country
1
Brief Summary
Attention-Deficit/Hyperactivity Disorder (ADHD) is a lifelong neurodevelopmental disorder characterised by persistent symptoms of inattention, hyperactivity, and impulsivity. According to the DSM-5, these symptoms must be present for at least six months, have an onset in childhood, and result in significant impairment in multiple life domains. Although ADHD may be limited to childhood in some cases, most individuals continue to have symptoms and impairments in varying degrees in adult life. The prevalence of persistent ADHD among adults is estimated to be approximately 2.58%, depending on diagnostic criteria and sample selection. The increasing awareness of ADHD has led to a marked increase in referrals to mental health services, which places greater demands on the development of effective and accessible treatment options for this group. Pharmacological treatment, particularly the use of stimulants, is a common intervention for adults with ADHD and has been shown to be effective for many. However, there are also side effects associated with drug treatment, and there is a need for more evidence-based non-drug alternatives. In addition, discontinuation of medication is common in ADHD treatment. Psychological interventions include psychoeducation and cognitive behaviour therapy, as well as more specialised approaches based on Dialectical Behaviour Therapy and Goal Management Training, which aim to improve executive functions. Whilst pharmacotherapy and psychotherapeutic interventions help some people with ADHD, not all people experience favourable outcomes, which calls for alternative treatment approaches. Interventions targeting the core symptoms of ADHD, executive functions, and behaviour are particularly relevant to treatment provision. One approach to improving executive functioning that has received increasing attention is physical exercise. Studies have shown that physical activity can have a positive effect on cognitive function, executive control, and behaviour in children and adolescents with ADHD. Physical exercise may also be applied as treatment for comorbid factors common in ADHD, such as mood disorders and multiple long-term physical conditions. Despite increasing interest in physical activity as a treatment modality, research on physical exercise for adults with ADHD is still limited. The findings from studies on younger age groups point to the potential for similar effects in adults, but more research is needed to examine the effects of physical exercise as a targeted intervention in the adult population with ADHD. Among the different types of physical activity, high-intensity interval training (HIIT) has gained promise for mental health. Due to its rapid, alternating, and fast-paced style, it could prove useful for those with ADHD. However, research on high-intensity interval training interventions (HIIT) in this population is scarce. To address these unanswered questions, this project will conduct a feasibility trial for a randomised controlled trial (RCT) to assess the feasibility and acceptability of HIIT among people with ADHD.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Feb 2026
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 15, 2026
CompletedStudy Start
First participant enrolled
February 1, 2026
CompletedFirst Posted
Study publicly available on registry
June 30, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
June 30, 2027
June 30, 2026
June 1, 2026
1.3 years
January 15, 2026
June 26, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (5)
Feasibility of the intervention: Recruitment rate
Recruitment rate: Proportion of eligible participants who agree to participate in the study ((Number of participants recruited/Number of eligible participants) x 100). Aim: \>50%.
through study completion, an average of 1 year
Feasibility measure: Retention rate
Retention rate: Proportion of participants who remain in the study until completion ((Number of participants completing the study/Number of participants enrolled) x 100). Aim: \>80%.
through study completion, an average of 1 year
Feasibility measure: Dropout rate
Dropout rate: How many participants dropped out after inclusion. Registration of reasons of dropout.
through study completion, an average of 1 year
Feasibility measure: Compliance
Compliance: How many sessions each participant attended. Registration of reasons of sessions not attended.
through study completion, an average of 1 year
Feasibility measure: Adherence to protocol
Adherence to protocol: How many elements in the physical exercise program were conducted in each session. Physical exercise diary for registration of load and intensity of strength- and endurance training, respectively. Aim: \>80%. Also, registration of adherence to the total test protocol.
through study completion, an average of 1 year
Secondary Outcomes (17)
In depth interview
Participants are inviteted within two weeks after ending their participation
General Ability - WAIS-IV
Within two weeks before initating intervention.
The Adult ADHD Self-Report Scale
Within two weeks before initating intervention. Within two weeks after ending intervention.
The Working Memory Questionnaire
Within two weeks before first intervention session and within two weeks after completion of the last session.
The Generalized Anxiety Disorder-7
Within two weeks before first intervention session and within two weeks after completion of the last session.
- +12 more secondary outcomes
Study Arms (1)
High intensity training
EXPERIMENTALFourteen weeks of high intensity strenght and endurance training after a protocol.
Interventions
14 weeks of high intensity training of strenght and endurace.
Eligibility Criteria
You may qualify if:
- Above 18 years
- An ADHD diagnosis (F90.0 in the ICD-10)
You may not qualify if:
- Psychiatric conditions not compatible with participation incl. ongoing psychotic episode, mania, acute suicidality etc.,
- Physical conditions precluding participation in physical testing and/or exercise
- Comprehensive ongoing substance use determined by the Alcohol Use Disorders IdentificationTest (AUDIT; Babor et al., 2001) and the Drug Use Disorder Identification Test (DUDIT; Berman et al., 2003). An AUDIT cut-off score of 16 (high risk), and/or DUDIT score of 20 (high risk) will lead to screening with MINI International Neuropsychiatric Interview (Lecrubier etal., 1997; Sheehan et al., 1998).
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Solli Distriktspsykiatriske Senterlead
- Helse Bergen Hospital Trustcollaborator
Study Sites (1)
Solli DPS and Kronstad DPS
Bergen, Norway
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Kristine Sirevåg, PhD
Solli DPS
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 15, 2026
First Posted
June 30, 2026
Study Start
February 1, 2026
Primary Completion (Estimated)
June 1, 2027
Study Completion (Estimated)
June 30, 2027
Last Updated
June 30, 2026
Record last verified: 2026-06
Data Sharing
- IPD Sharing
- Will not share
This has not been applied for to the ethical Committee.