Multi-Component Training Versus Motor Learning Techniques in Adults With ADHD
MCT-MLT
Comparative Effects of Multi-Component Training and Motor Learning Techniques on Attention, Cognitive Performance, and Motor Coordination in Adults With Attention Deficit Hyperactivity Disorder
1 other identifier
interventional
44
1 country
1
Brief Summary
This randomized clinical trial aims to compare the effects of multi-component training and motor learning techniques on attention, cognitive performance, and motor coordination in adults with Attention Deficit Hyperactivity Disorder (ADHD). ADHD in adults is associated with impairments in executive function, attention regulation, and motor coordination, which significantly impact daily functioning and quality of life. While pharmacological and behavioral therapies are commonly used, non-pharmacological interventions such as structured exercise and motor learning approaches have shown potential benefits. A total of 44 participants aged 18-30 years with clinically diagnosed ADHD will be recruited and randomly allocated into two groups. Group A will receive multi-component training including aerobic, resistance, balance, and flexibility exercises, while Group B will receive motor learning techniques focusing on task-oriented and cognitive-motor dual-task training. Both interventions will be administered three times per week for eight weeks. Outcome measures will include standardized tools assessing attention, executive function, and cognitive performance, including ADHD rating scales and cognitive assessments. Data will be analyzed pre- and post-intervention to determine within-group and between-group differences. This study aims to identify effective, non-pharmacological rehabilitation strategies for improving cognitive and motor outcomes in adults with ADHD.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Sep 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 1, 2026
CompletedStudy Start
First participant enrolled
September 10, 2026
CompletedFirst Posted
Study publicly available on registry
September 29, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 10, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 10, 2026
September 29, 2026
September 1, 2026
3 months
June 1, 2026
September 27, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Conners' Adult ADHD Rating Scale
Adult ADHD symptom severity will be assessed using the Conners' Adult ADHD Rating Scales (CAARS).
8 weeks of treatment (Pre & Post)
Secondary Outcomes (2)
Purdue Pegboard Test
Baseline and immediately after completion of the 8-week intervention
Trial Making Test
8 weeks of intervention (Pre & Post)
Study Arms (2)
Multi-Component Training Group
EXPERIMENTALParticipants in this group will receive multi-component training including warm-up, aerobic training, resistance training, balance and flexibility exercises, breathing exercises, and cool-down. Sessions will be conducted three times per week for 8 weeks, with each session lasting approximately 30-40 minutes.
Motor Learning Techniques Group
ACTIVE COMPARATORParticipants in this group will receive motor learning techniques including warm-up, task-oriented training, cognitive-motor dual-task activities, feedback-based learning, and cool-down. Sessions will be conducted three times per week for 8 weeks, with each session lasting approximately 30-40 minutes.
Interventions
Multi-component training will include warm-up, moderate-intensity aerobic exercise, resistance training using light weights or resistance bands, balance and flexibility exercises, breathing exercises, and cool-down. Sessions will be supervised three times per week for 8 weeks, with each session lasting approximately 30-40 minutes.
Motor learning techniques will include warm-up, task-oriented functional motor activities, cognitive-motor dual-task exercises, feedback-based learning, and cool-down. Sessions will be supervised three times per week for 8 weeks, with each session lasting approximately 30-40 minutes.
Eligibility Criteria
You may qualify if:
- Male and female adults aged 18 to 30 years.
- Clinically diagnosed with Attention Deficit Hyperactivity Disorder.
- Adult ADHD Self-Report Scale score indicating ADHD symptoms.
- Montreal Cognitive Assessment score less than 26 out of 30.
- Medically stable and able to participate in moderate physical activity.
- Not currently participating in any other structured cognitive or physical intervention program.
- Able to attend supervised sessions three times per week for 8 weeks.
- Willing to provide written informed consent.
You may not qualify if:
- History of systemic or neurological disorders.
- Currently undergoing treatment for ADHD or participating in similar interventions.
- Physical limitations preventing participation in physical activity.
- Severe psychiatric conditions such as schizophrenia or bipolar disorder.
- Uncontrolled cardiovascular conditions or medical contraindications to moderate physical activity.
- Taking medications that significantly alter cognitive or motor performance unless stabilized for at least 3 months.
- History of substance abuse within the past 12 months.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Shalamar Hospital and Ali Hospital
Lahore, Punjab Province, 54000, Pakistan
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Wajeeha zia
Riphah International University Role
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Masking Details
- The outcome assessor will be blinded to group allocation. Participants and care providers will not be blinded due to the nature of the rehabilitation interventions.
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 1, 2026
First Posted
September 29, 2026
Study Start
September 10, 2026
Primary Completion (Estimated)
December 10, 2026
Study Completion (Estimated)
December 10, 2026
Last Updated
September 29, 2026
Record last verified: 2026-09
Data Sharing
- IPD Sharing
- Will not share