Young AdultsNCT05243095
Computer-Assisted, Game-Based Cognitive Training on Attention
A study testing Computer assited, game-based cognitive training in people with Young Adults and Attention, run by Pamukkale University at 1 site in Turkey (Türkiye).
Trial summary
The aim of this study was to investigate the effect of 8 weeks of cognitive training on attention function in healthy young people. Read more about this study
- Who is it for?
- Ages 21 to 24 yearsHealthy volunteers can take part
- Conditions the study is for
- Young Adults, Attention
- What is being tested?
- Computer assited, game-based cognitive training
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 60 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 15 Feb 2022to 10 May 2022
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 21 to 24 years
- All sexes
- Healthy volunteers accepted
- Adult
Who may be able to join
- Those between the ages of 21-24,
- No communication problem,
- Not continuing any exercise program for the last 1 year,
- Having a smart phone, tablet or computer required to participate in the training program,
- Individuals who volunteered to participate in the study.
Who cannot join
- Having vision and hearing problems,
- Individuals who continued the physical exercise program and/or had hobbies such as puzzles and jigsaw puzzles that could affect the cognitive level.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: The Effect of Computer-Assisted, Game-Based Cognitive Training on Attention: A Randomized Controlled Study
The aim of this study was to investigate the effect of 8 weeks of cognitive training on attention function in healthy young people.
- Conditions
- Young Adults, Attention
- Being tested
- Computer assited, game-based cognitive training
- Keywords
- Cognitive-training
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Computer assited, game-based cognitive trainingOther
After recording the demographic information of the participants, the Stroop Test was applied to evaluate attention. After the stages of the test were explained to the participants in detail, they were shown once in practice.
The training group received 20 minutes of cognitive training every day for 8 weeks. No training was applied to the control group. Groups were evaluated at baseline and after 8 weeks.
| Study group | Role | What they receive |
|---|---|---|
| Cognitive training group | Experimental | The training group received 20 minutes of cognitive training every day for 8 weeks Receives: Other: Computer assited, game-based cognitive training |
| Control group | No intervention | No training was applied to the control group. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Stroop test
The Stroop Test is a test that evaluates frontal lobe functions and cognitive processes such as attention and information processing.
The Stroop Test TBAG Form consists of four white cards measuring 14.0 x 21.5 cm.
The performance of the participants was scored according to three separate criteria for each section: These criteria are: the time taken until the last item of the section is answered with the "start" command, the number of errors, the number of corrected responses.
Measured: 10 minutes
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted16 Feb 2022
- Study start15 Feb 2022
- Primary completion20 Apr 2022
- Study completion10 May 2022
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Young AdultsStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 60 participants (actual)
Sponsor and investigators
- Lead sponsor
- Pamukkale University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Ayşe Ünal, Pamukkale University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05243095
- Sponsor's protocol ID
- 27.01.2022/Attention
- Status last verified
- Oct 2022
- First submitted
- 27 Jan 2022
- Last updated
- 21 Oct 2022
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 21 Oct 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effect of Computer-Assisted, Game-Based Cognitive Training on Attention: A Randomized Controlled Study
- ClinicalTrials.gov ID
- NCT05243095
- Acronym / sponsor ID
- 27.01.2022/Attention
- Conditions
- Young Adults, Attention
- Keywords
- Cognitive-training
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 60 participants (actual)
- Lead sponsor
- Pamukkale UniversityUniversity, hospital or other
- Study start
- 15 Feb 2022 (actual)
- Primary completion
- 20 Apr 2022 (actual)
- Study completion
- 10 May 2022 (actual)
- First posted
- 16 Feb 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The aim of this study was to investigate the effect of 8 weeks of cognitive training on attention function in healthy young people.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Cognitive training group | Experimental | Other: Computer assited, game-based cognitive trainingThe training group received 20 minutes of cognitive training every day for 8 weeks |
| Control group | No intervention | –No training was applied to the control group. |
Who may qualify
- Ages
- 21 to 24 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (5 listed)
- Those between the ages of 21-24,
- No communication problem,
- Not continuing any exercise program for the last 1 year,
- Having a smart phone, tablet or computer required to participate in the training program,
- Individuals who volunteered to participate in the study.
Key exclusion criteria (2 listed)
- Having vision and hearing problems,
- Individuals who continued the physical exercise program and/or had hobbies such as puzzles and jigsaw puzzles that could affect the cognitive level.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Computer assited, game-based cognitive trainingAfter recording the demographic information of the participants, the Stroop Test was applied to evaluate attention. After the stages of the test were explained to the participants in detail, they were shown once in practice. The training group received 20 minutes of cognitive training every day for 8 weeks. No training was applied to the control group. Groups were evaluated at baseline and after 8 weeks. | Other | Cognitive training group |
Primary outcome
Stroop test
Time frame: 10 minutes
The Stroop Test is a test that evaluates frontal lobe functions and cognitive processes such as attention and information processing. The Stroop Test TBAG Form consists of four white cards measuring 14.0 x 21.5 cm. The performance of the participants was scored according to three separate criteria for each section: These criteria are: the time taken until the last item of the section is answered with the "start" command, the number of errors, the number of corrected responses.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 21 Oct 2022.
- Individual participant dataSharing planned: No
Related trials for Young Adults
RecruitingPhase 2
Trastuzumab Deruxtecan (DS-8201a) for the Treatment of Recurrent or Refractory Osteosarcoma, Wilms Tumor, and Desmoplastic Small Round Cell Tumor
Desmoplastic Small Round Cell Tumor, Osteosarcoma
RecruitingPhase 2
Illuminate: A Clinical Study Evaluating CAR T Immune Cell Therapy (BCB-276) for Patients With Diffuse Intrinsic Pontine Glioma (DIPG).
Diffuse Intrinsic Pontine Glioma, DIPG
Recruiting
The Young Adults' Experiences With Virtual Reality (YAES VR) Study
Population Health
RecruitingObservational study
NCI Childhood Cancer Data Initiative (CCDI) Led Pediatric, Adolescent, and Young Adult Rare Cancer Registry for Very Rare Solid Tumors
Very Rare Tumors, Very Rare Cancers
Not yet recruiting
Using Virtual Reality to Augment Brief Interventions for Heavy Drinking Young Adults
Alcohol Misuse
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Computer assited, game-based cognitive training in people with Young Adults and Attention, run by Pamukkale University at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 21 Oct 2022. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Stroop test (time frame: 10 minutes). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Oct 2022.