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Psycho-educational Program to Enhance Alerting Consciousness and Seeking Support Among Family Caregivers Having Children With Autism

18 maja 2026 zaktualizowane przez: nora said, Ain Shams University

The goal of this study is to evaluate the effect of a psycho-educational program to enhance alert consciousness and seeking support among family caregivers having children with autism. In a purposive sample of male participants diagnosed with autism. Aged from 6 to 12 years old (school age). Hypothesis:

A psycho-educational program will have a positive effect after implementation on enhancing alerting consciousness and seeking support among family caregivers having children with autism.

A quasi-experimental one-group pretest-post-test design was used

Przegląd badań

Status

Zakończony

Szczegółowy opis

  1. Introduction and Rationale According to the World Health Organization (WHO), the prevalence of ASD worldwide is 1 in every 100 children. The prevalence of ASD in Egypt is estimated at 5.4/1000 among Egyptian children. Children with ASD impose distinct challenges on their family caregivers due to being unable to cope effectively, including financial, physical, and psychological challenges, which can lead to significant stress, burden, and pessimism. So, it's important for a psychoeducational program to support caregivers who have children with ASD to deal with their psychological problems as well as find alerting consciousness and seek support that increases their life satisfaction and quality of life that enables caregivers to deal with their children suffering.

    Caregivers can employ both sorts of coping strategies concurrently, and their efficacy can impact the overall welfare of the family. These include seeking guidance and assistance from healthcare professionals and support groups, establishing regular routines and structures in daily life, and engaging in mindfulness and relaxation techniques. In addition, certain caregivers may employ alerting consciousness. It is crucial to acknowledge that the efficacy of coping methods might differ among parents, and the selection of coping strategy may be influenced by the individual's personal traits, the intensity of the child's symptoms, and the presence of social support.

    This study aimed to evaluate the effect of a psycho-educational program to enhance alert consciousness and seeking support among family caregivers having children with autism.

  2. Study Objectives and Hypothesis

    Primary Aim: evaluate the effect of a psycho-educational program to enhance alert consciousness and seeking support among family caregivers having children with autism.

    Primary Hypothesis: A psycho-educational program will have a positive effect after implementation on enhancing alerting consciousness and seeking support among family caregivers having children with autism.

  3. Methods 3.1. Study Design: A quasi-experimental, one-group pre-test/post-test design was employed.

3.2. Setting: at an autistic center affiliated to El-Abbasia psychiatric and mental Hospital in Cairo, Egypt.

3.3. Participants: A purposive sample of family caregivers of children with autism registered in the previously mentioned setting was recruited. Inclusion criteria were related to the child: Age from 6 to 12 years old (school age) and No neurological or physical disorders or disability. Also, regarding to family caregivers: Be the primary caregiver at the same home and provide direct care for the children at least 1 year, and don't have other children with special needs or disabilities.

Sample size was determined via power analysis (α=0.05, β=0.15) based on a previous study.

3.4. Intervention (a psycho-educational program): The researcher-developed program, reviewed by supervisors and grounded in literature, comprised 11 core sessions (4 theoretical, 7 practical) plus orientation and closure sessions, delivered over 45 to 60 minutes each.

Theoretical Component (Sessions 1-4): Covered autism, management plans, challenges confronting family caregivers

Practical Component (Sessions 5-11): Focused on applied across three domains:

Optimism (Sessions 5): Optimism, definitions, concepts, and strategies for enhancement

Coping patterns (Sessions 6-11): Stress management, meditation, problem solving, relaxation techniques, and mindfulness.

Pedagogy: Interactive methods were used, including open discussions, brainstorming, role-playing, demonstrations, videos, and handouts. Each session included homework review, feedback, objective setting, and a Q&A period.

3.5. Data Collection Tools:

Tool I: Interview Questionnaire Collected socio-demographic and clinical data For the child: age in years, gender, number of siblings, child order, and level of education.

For family caregivers: Age, gender, marital status, level of education, degree of contingency, occupation, residence, and income.

Tool II: Clinical data tool: : assesses clinical data for children with autism such as enrollment in the behavioral modification program and onset of diagnosis. And family history of psychiatric or mental illness.

Tool III: Brief-COPE inventoryIt was used to assess alerting consciousness and seeking support among family caregivers of children with ASD. It consists of 28 items presented in the form of a coping statement, and the responses ranged from: I have not been doing this at all (1), to I have been doing this a lot (4). scoring system: ;The alerting consciousness and seeking support of the caregivers of children with autism were considered ineffective if the score was < 50% and effective if the percent score was ≥ 50%.Demonstrated high reliability in this study (Cronbach's α = 0.968).

3.6. Data Collection Procedure: The 6-month study (Feb-June 2025) followed stages: ethical approvals, baseline (pre-test) data collection using Tools I and II, program implementation n=50 post-test) 3.7. Statistical Analysis: Data were analyzed using SPSS v26. Descriptive statistics (frequencies, percentages, means, standard deviations) described the sample. A paired t-test was used to compare pre- and post-intervention self-efficacy scores, with a significance level of p < 0.05.

Ethics: Approved by the Faculty of Nursing, Ain Shams University IRB (ID: 26.041229). Informed consent was obtained from all participants

Typ studiów

Interwencyjne

Zapisy (Rzeczywisty)

50

Faza

  • Nie dotyczy

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Lokalizacje studiów

    • El Abbasia
      • Cairo, El Abbasia, Egipt, 11511
        • El Abbasia Mental Health Hospital
      • Cairo, El Abbasia, Egipt, 11511
        • faculty of Nursing Ain Shams University

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dziecko
  • Dorosły
  • Starszy dorosły

Akceptuje zdrowych ochotników

Nie

Opis

Inclusion Criteria:

  • Family has a child with characteristics:

    • Age from 6 to 12 years old (school age).

  • Family caregivers with characteristics:

    • Be the primary caregiver at the same home and provide direct care for the children for at least 1 year.

Exclusion Criteria:

  • Family has child with neurological or physical disorders or a disability and doesn't have other children with special needs or disability

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Badania usług zdrowotnych
  • Przydział: Nie dotyczy
  • Model interwencyjny: Zadanie dla jednej grupy
  • Maskowanie: Brak (otwarta etykieta)

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Inny: Quasi-experimental one group Pre-post test

11 core sessions to enhance alerting consciousness and seeking support among family caregivers having children with autism (4 theoretical, 7 practical) plus orientation and closure sessions, delivered over 45 to 60 minutes each.

Theoretical Component (Sessions 1-4): Covered autism, management plans, challenges confronting family caregivers. Practical Component (Sessions 5-11): Focused on application across three domains: Optimism (Session 5): Optimism, definitions, concepts, and strategies for enhancement. Coping patterns (Sessions 6-11): Stress management, meditation, problem-solving, relaxation techniques, and mindfulness.

This study aims to assess the impact of a psychoeducational program on Enhance Alerting Consciousness and Seeking Support among Family Caregivers Having Children with Autism. The program is designed to levels of alert consciousness, seeking support, overcome the challenges.

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Structured interview questionnaire
Ramy czasowe: The assessment period for each participant was 12 weeks from the start of their participation in the study.

For the child: age in years, gender, number of siblings, child order, and level of education.

For family caregivers: age, gender, marital status, level of education, degree of contingency, occupation, residence, and income.

The assessment period for each participant was 12 weeks from the start of their participation in the study.
Clinical data tool
Ramy czasowe: The assessment period for each participant was 12 weeks from the start of their participation in the study.
clinical data for children with autism, such as enrollment in the behavioral modification program and onset of diagnosis. And family history of psychiatric or mental illness.
The assessment period for each participant was 12 weeks from the start of their participation in the study.

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Brief-COPE inventory
Ramy czasowe: The assessment period for each participant was 12 weeks from the start of their participation in the study.
It was used to assess alerting consciousness and seeking support among family caregivers of children with ASD. It consists of 28 items presented in the form of a coping statement, and the responses ranged from "I have not been doing this at all" (1) to "I have been doing this a lot" (4).
The assessment period for each participant was 12 weeks from the start of their participation in the study.

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Śledczy

  • Główny śledczy: Nora Sa Mohamed, Assist/Lec, Psychiatric/ Mental Health Nursing department Faculty of Nursing - Ain Shams University
  • Krzesło do nauki: Omayma Ab Osman, Professor, Psychiatric/ Mental Health Nursing department Faculty of Nursing - Ain Shams University
  • Dyrektor Studium: Afaf Mo Fahmy, Assist/Prof, Psychiatric/Mental Health Nursing , Faculty of Nursing Ain Shams University-Cairo-Egypt.
  • Dyrektor Studium: Hanaa Ez Eldin Prince, Assist/Prof, Psychiatric/Mental Health Nursing , Faculty of Nursing Ain Shams University-Cairo-Egypt.

Publikacje i pomocne linki

Osoba odpowiedzialna za wprowadzenie informacji o badaniu dobrowolnie udostępnia te publikacje. Mogą one dotyczyć wszystkiego, co jest związane z badaniem.

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Rzeczywisty)

11 lutego 2025

Zakończenie podstawowe (Rzeczywisty)

30 kwietnia 2025

Ukończenie studiów (Rzeczywisty)

1 czerwca 2025

Daty rejestracji na studia

Pierwszy przesłany

18 maja 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

18 maja 2026

Pierwszy wysłany (Rzeczywisty)

22 maja 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

22 maja 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

18 maja 2026

Ostatnia weryfikacja

1 maja 2026

Więcej informacji

Terminy związane z tym badaniem

Plan dla danych uczestnika indywidualnego (IPD)

Planujesz udostępniać dane poszczególnych uczestników (IPD)?

TAK

Opis planu IPD

Study Protocol, Informed Consent Form (ICF), all IPD that underlie results in a publication

Ramy czasowe udostępniania IPD

present

Typ informacji pomocniczych dotyczących udostępniania IPD

  • PROTOKÓŁ BADANIA
  • ICF

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Nie

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

Badania kliniczne na Zaburzenia ze spektrum autyzmu

Badania kliniczne na Psycho-educational Program

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