Psychological Counseling Program for Alzheimer's Patients' Caregivers

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorAydan Akkurt Yalçıntürk

About this trial

Purpose: To investigate the effects of a psychological counseling program (PsychoCP) applied to caregivers of Alzheimer's patients on perceived stress, psychological well-being and care burden.

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Providing informal care to an individual with mild or moderate Alzheimer's disease

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

Disqualifiers

Not being able to understand questions and express ideas

Having a psychiatric disorder

Not receiving any therapy services during the study

Trial design

Design model

Parallel

Treatments tested in this trial

  • Psychological Counseling Program

    Other intervention

    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.

Treatment groups

80 Participants
are divided into 2 treatment groups
Group A: PsychoCPExperimental treatment 1 intervention
Group B: ControlNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Perceived Stress Level

Perceived Stress Scale: It was developed to measure the stress level of specific situations in individuals' lives. This scale consists of 14 items and is evaluated by participants on a 5-point Likert-type scale ranging from "never (0)" to "very often (4)". The score range of the scale is 0-56. High scores obtained from the scale indicate that the individual's perceived stress level is high.

Time frame
Two months
2

Psychological Well-being Level

Psychological Well-being Scale: It is a scale that evaluates the psychological well-being of an individual. The items of the scale are rated between 1 and 7 as strongly disagree (1) and strongly agree (7). The minimum score is 8 and the maximum score is 56. An increase in the score value indicates that the person has many psychological resources and strengths.

Time frame
Two months
3

The Burden of Caregiving

Zarit Caregiver Burden Scale: The scale is used to measure the stress of caregivers. It contains 22 Likert-type statements. The statements range from zero to four as never (0), rarely (1), sometimes (2), quite often (3), almost always (4). A minimum of 0 and a maximum of 88 points can be obtained from the scale. As the score value increases, the stress experienced by the caregiver also increases.

Time frame
Two months

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Aydan Akkurt Yalçıntürk

Lead sponsor

Uskudar University

Sponsor institution

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