The Effect of Memory-Based Exercise and Planned Training Applied to Epilepsy Patients on Quality of Life
NCT ID: NCT06954922
Last Updated: 2025-05-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
NOT_YET_RECRUITING
NA
50 participants
INTERVENTIONAL
2025-05-31
2026-01-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
The patient introduction form and the Quality of Life in Epilepsy Scale will be administered to the patients in both groups by the researcher using the face-to-face interview technique (pre-test). Patients in the experimental group will be informed about memory-based exercise and planned training.
Patients in the control group will only be informed about the planned training to be given.
The experimental group will be given memory-based exercises that will last approximately 15-20 minutes every day for 2 months. Four sessions of epilepsy training will be given, one session per week.
The control group will receive 4 sessions of epilepsy training, one session per week.
At the end of two months, the Quality of Life in Epilepsy Scale (posttest) will be applied to both groups.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
The Effect of Progressive Relaxation Exercises Applied to Patients With Epilepsy
NCT05127499
Physical Exercise in Subjects With Juvenile Myoclonic Epilepsy
NCT01450423
Sensory Modulation in Children With Epilepsy
NCT06818344
Examining the Effect of Metaverse-Based Epilepsy Education
NCT06195020
Impact of Educational Actions on the Quality Of Life of Epileptic Patients
NCT02832349
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
SEQUENTIAL
HEALTH_SERVICES_RESEARCH
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
memory-based exercise and training group
memory-based exercise and training intervention
The experimental group will be given memory-based exercises that will last approximately 15-20 minutes every day for 2 months. Four sessions of epilepsy training will be given, one session per week.
training group
educational initiative about epilepsy
This group will be given 4 sessions of epilepsy training, one session per week.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
memory-based exercise and training intervention
The experimental group will be given memory-based exercises that will last approximately 15-20 minutes every day for 2 months. Four sessions of epilepsy training will be given, one session per week.
educational initiative about epilepsy
This group will be given 4 sessions of epilepsy training, one session per week.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. Being over the age of 18,
3. Having sufficient communication skills to answer oral and written questions and follow instructions,
4. Being at a cognitive level to be able to use a mobile phone and perform the memory exercise.
5. Not having severe vision problems,
6. Having been diagnosed with epilepsy for at least 6 months
Exclusion Criteria
2. Residing outside Bilecik Province
3. Having psychiatric diagnoses such as Bipolar Disorder and Schizophrenia
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Ataturk University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
AHMET ŞİMŞEK
PhD student
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
ATAÜNİ-SBE-AS-02
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.