Psychological Counseling Program for Alzheimer's Patients' Caregivers
NCT ID: NCT06755476
Last Updated: 2025-01-01
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
80 participants
INTERVENTIONAL
2025-02-15
2025-08-15
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Design: The study will be conducted in a pre-test post-test control group, randomized controlled experimental research design.
Method: The study is planned to be carried out in Bağcılar Municipality Vefahâne Life Center, Antalya Alzheimer Patients and Patient Relatives Meeting Center and Osmaniye Family and Social Policies Directorate. The sample of the study will consist of 80 caregivers. They will be assigned to intervention (n=40) and control groups (n=40) by randomization.
Hypotheses Hypothesis1: The perceived stress level of caregivers who received PsychoDP is lower than those who did not receive PsychoCP.
Hypothesis2: The psychological well-being levels of caregivers who received PsychoDP are higher than those who did not receive PsychoCP.
Hypothesis3: The care burden of caregivers who received PsychoDP is lower than those who did not receive PsychoCP.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Evaluation of the Structured Caregiver Support Program (SCSP) in Terms of Various Parameters
NCT05990114
The Effect of Person-Centered Care Applied to Patients With Dementia on Nutritional Status
NCT06191172
Early Counseling and Support for Alzheimer's Disease Caregivers
NCT02685787
The Progressively Lowered Stress Threshold Model
NCT04305652
THE EFFECT OF REMOTE NURSING INTERVENTIONS BASED ON THE EMPOWERMENT PROCESS MODEL ON PEOPLE WITH DEMENTIA AND THEIR FAMILY CAREGIVERS
NCT07010874
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
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
PsychoCP
Psychological Counseling Program
The Psychological Counseling Program consists of 8 sessions for caregivers of individuals diagnosed with Alzheimer's.
Aims of the sessions:
Session 1: Introduction, Collection of pretest data Session 2: It is aimed to inform Alzheimer's caregivers about the disease and its symptoms.
Session 3: It is aimed to strengthen caregivers' coping skills. Session 4: It is aimed to inform Alzheimer's patients about daily care practices.
Session 5: It is aimed to provide information to Alzheimer's caregivers about coping with stress.
Session 6: It is aimed to provide information about medical and financial support that individuals diagnosed with Alzheimer's and their relatives can receive in the region they live.
Session 7: It is aimed to conduct Q\&A sessions on the problems that caregivers bring.
Session 8: Collection of posttest data Sessions will be completed in 8 weeks, one day a week. Each session is planned to last approximately 60 minutes.
Control
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Psychological Counseling Program
The Psychological Counseling Program consists of 8 sessions for caregivers of individuals diagnosed with Alzheimer's.
Aims of the sessions:
Session 1: Introduction, Collection of pretest data Session 2: It is aimed to inform Alzheimer's caregivers about the disease and its symptoms.
Session 3: It is aimed to strengthen caregivers' coping skills. Session 4: It is aimed to inform Alzheimer's patients about daily care practices.
Session 5: It is aimed to provide information to Alzheimer's caregivers about coping with stress.
Session 6: It is aimed to provide information about medical and financial support that individuals diagnosed with Alzheimer's and their relatives can receive in the region they live.
Session 7: It is aimed to conduct Q\&A sessions on the problems that caregivers bring.
Session 8: Collection of posttest data Sessions will be completed in 8 weeks, one day a week. Each session is planned to last approximately 60 minutes.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Being a primary caregiver
* Providing care to the patient for at least six months
* Providing care to the patient for at least six hours per day
* Being literate
* Being able to speak and understand Turkish
* Being 18 years of age or older
* Being willing and able to participate in the study
Exclusion Criteria
* Having a psychiatric disorder
* Not receiving any therapy services during the study
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Aydan Akkurt Yalçıntürk
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Aydan Akkurt Yalçıntürk
Asst. Prof.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
20122024
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.