Effects of an Aerobic Exercise Intervention on Core Symptoms, Executive Functioning, and Quality of Life in Children With Attention Deficit Hyperactivity Disorder

NCT ID: NCT06553430

Last Updated: 2024-08-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-11-28

Study Completion Date

2024-11-30

Brief Summary

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Selecting a maternal and child healthcare hospital in Shenzhen City, Guangdong Province, 50 cases of ADHD children as the study subjects, according to the inclusion and exclusion criteria to screen the eligible study subjects, introduction of the purpose and process of the study, informed consent to enrolment, the children were divided into the intervention group and the control group. The experimental group used aerobic exercise, while the control group was given daily physical activity, and general information questionnaires, Conners Parental Symptom Questionnaire, SNAP-IV scale, Stroop Colour Word Test, Rey Complex Graphics Test, Connection Test, Children's Depressive Disorder Self-assessment Scale, Children's Anxious Mood Disorder Screening Scale, Children's Quality of Life Universal Core Scale, and Children's Executive Functioning Questionnaire were assessed.

Detailed Description

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Purposive sampling method was used to select a maternal and child healthcare hospital in Shenzhen City, Guangdong Province, 50 cases of ADHD children as the study subjects, according to the inclusion and exclusion criteria to screen the eligible study subjects, introduction of the purpose and process of the study, informed consent to enrolment, the children were divided into age, gender, clinical typing, medication use, family proximity, Conners scores and SNAP-IV scores matching the intervention group and the control group. The experimental group used aerobic exercise, while the control group was given daily physical activity, and general information questionnaires, Conners Parental Symptom Questionnaire, SNAP-IV scale, Stroop Colour Word Test, Rey Complex Graphics Test, Connection Test, Children's Depressive Disorder Self-assessment Scale, Children's Anxious Mood Disorder Screening Scale, Children's Quality of Life Universal Core Scale, and Children's Executive Functioning Questionnaire were assessed.

Conditions

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ADHD

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Intervention group

Moderate-intensity aerobic exercise for 30-60 min 3 times per week for 12 weeks and daily physical activity

Group Type EXPERIMENTAL

aerobics exercises

Intervention Type BEHAVIORAL

Moderate-intensity aerobic exercise for 30-60 min 3 times per week for 12 weeks

Control group

daily physical activity

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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aerobics exercises

Moderate-intensity aerobic exercise for 30-60 min 3 times per week for 12 weeks

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Children clinically diagnosed with ADHD;
* 7-14 years old;
* Combined Raven's Test ≥ 80;
* Not participating in any treatment other than drug therapy;
* The body can participate in sports training;
* The type of family intimacy is intimate or above;
* Voluntarily participate and sign an informed consent form

Exclusion Criteria

* Children with a history of epileptic seizures;
* Children with other mental or motor disorders;
* Children with visual impairments;
* Using other psychotropic drugs;
* Have other comorbidities;
* Merge other serious chronic diseases (such as severe heart, brain, kidney, lung, etc.), tumors, etc
Minimum Eligible Age

7 Years

Maximum Eligible Age

14 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Harbin Medical University

OTHER

Sponsor Role lead

Responsible Party

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Lingrong Xiao

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Nanshan Maternal and Child Health Hospital

Guangzhou, Shenzhen, China

Site Status RECRUITING

Countries

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China

Facility Contacts

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Gang Zhao

Role: primary

17382797561

Other Identifiers

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LXiao

Identifier Type: -

Identifier Source: org_study_id

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