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Hubungan Lama Hemodialisa Dengan Care Dependency Pada Pasien Gagal Ginjal Kronik Yang Menjalani Terapi Hemodialisis Di Rsud Dr. Abdoer Rahem Wahyuni, Ida; Tri Nili Sulayfiyah; Mery Eka Yaya Fujianti; Rohman, Atiqur; Bergita Dumar
Indonesian Health Science Journal Vol. 4 No. 2 (2024): Oktober
Publisher : Universitas Nazhatut Thullab Al- Muafa Sampang

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.52298/ihsj.v4i2.60

Abstract

Background: Chronic kidney failure can cause psychological, physical and social activity disorders. Therapy that can preserve the kidneys is hemodialysis. Purpose: This study aims to determine the relationship between duration of hemodialysis and care dependency in CKD patients undergoing hemodialysis therapy. Care dependency was measured using the Care Dependency Scale (CDS). Method: The design of this research is descriptive quantitative with a cross sectional approach. The variables in this study are duration of hemodilsis and care dependency. The research sample was 109 respondents taken using a consecutive sampling technique. Data were analyzed using the Chi Square test. Results: The research results show that there is no relationship between the length of hemodialysis and care dependency with a p value > 0.05, which means there is no relationship between care dependency and the length of hemodialysis. Conclusions: Patients who have been undergoing hemodialysis for a long time will tend to have mild or moderate levels of stress, because of the length of time undergoing hemodialysis, patients are able to adapt themselves to the dialysis equipment and hemodialysis patients will find it easier to manage physical limitations in their daily lives.
Shame and Burden: Family Stigma in Caring for Shackled Individuals with Mental Disorders Holis, Willi; Rohman, Atiqur; Yaya, Mery Eka
Genius Journal Vol. 5 No. 2 (2024): GENIUS JOURNAL
Publisher : Inspirasi Foundation

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.56359/gj.v5i2.541

Abstract

Introduction: Mental disorders remain a significant public health concern, often leading to stigma and social discrimination, particularly for families caring for affected individuals. In some cases, shackling (physical restraint) is still practiced due to limited access to mental health services, further intensifying the burden on caregivers. Objective: This study aims to explore the family experiences of stigma and emotional burden in providing care for shackled individuals with mental disorders. Method: A qualitative research design with a phenomenological approach was employed. The study was conducted within the scope of the Pamekasan District Health Office, involving families of mentally ill patients as participants. Inclusion criteria included participants who had cared for restrained family members for over a year, were above 20 years old, willing to participate, and able to communicate verbally. A snowball sampling technique was used, where key informants assisted in identifying additional participants. Results: Participants reported experiencing stigma related to their role in caring for family members with mental disorders who had been restrained. The findings highlight psychological and emotional reactions, as well as how participants navigate daily life amid societal stigma. A key subtheme, "Emotions," describes their emotional responses, which include sadness, anger, shame, and guilt—common experiences among participants. Conclusion: This study concludes that family caregivers of individuals with mental illness face significant psychological distress due to stigma, primarily manifesting as sadness, anger, shame, and guilt. These emotional responses stem from discrimination, stereotyping, and societal labeling. Effective emotional management is crucial in helping caregivers cope and respond constructively to stigma. The findings emphasize the need for supportive interventions to enhance caregivers' emotional resilience and overall well-being.
Community Stigma toward Leprosy Patients Hidayat, Mukhlish; Hakim, Arif Rahman; Khalilah, Nur; Nur, Mohamad; Dewi, Novela Eka Candra; Rohman, Atiqur
TRILOGI: Jurnal Ilmu Teknologi, Kesehatan, dan Humaniora Vol 6, No 1 (2025)
Publisher : Universitas Nurul Jadid

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.33650/trilogi.v6i1.10814

Abstract

Leprosy is a chronic disease that rarely causes death but often causes disability. This disability leads to different opinions in the community, which disrupts the social life of leprosy sufferers and the surrounding community. In this study, the researcher wanted to examine more deeply the opinions of people with leprosy. This research design uses qualitative research that focuses on a phenomenological approach. The participants taken in this study were 11 people who had criteria where the location of the participant's house was not more than 100 meters from the leprosy patient. Participants were selected through purposive sampling and data collection techniques using in-depth interviews with the main instrument, namely the researcher himself and assisted by other instruments in the form of field notes, interview guidelines and sound recording devices. The results of this study resulted in three themes: (1) Factors that influence stigma towards leprosy patients (2) Perceptions of Leprosy Patients (3) Forms of Stigma towards Leprosy Patients. Community stigma still occurs against leprosy patients, this is due to the low level of education and knowledge of the community about leprosy, so there needs to be intervention by health workers to increase community knowledge so that the stigma felt by leprosy patients can be reduced.
Dampak Sosial Jetlag terhadap Kesehatan Remaja: A Scoping Review Rohman, Atiqur; Wahyuni, Ida; Sulayfiyah, Tri Nili
Jurnal Penelitian Perawat Profesional Vol 7 No 1 (2025): Februari 2025, Jurnal Penelitian Perawat Profesional
Publisher : Global Health Science Group

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.37287/jppp.v7i1.5857

Abstract

Remaja mengalami gangguan pola tidur/bangun yang disebut social jetlag. Gangguan ini merupakan gangguan ritme sirkadian yang melibatkan ketidakselarasan antara waktu biologis dan program sosial hal tersebut berdampak pada kesehatan dan proses perkembangan remaja. Berdasarkan hasil identifikasi sampai saat ini belum ada review yang mensintesis secara spesifik mengidentifikasi bukti-bukti studi tentang dampak risiko kesehatan yang terkait dengan social jetlag pada remaja. Tujuan dari penelitian ini untuk mengidentifikasi bukti-bukti terbaru mengenai dampak kesehatan terkait social jetlag pada remaja. Penelitian ini menggunakan pendekatan scoping review. Sumber literatur diperoleh melalui pencarian dengan menggunakan database yang terdiri dari PUBMED, Science Direct dan Scopus dari 2019-2023. Kriteria inklusi dalam pemilihan artikel yaitu 1) rentang publikasi artikel 5 tahun terakhir; 2) Bahasa inggris; 3) tema artikel terkait dengan dampak kronotipe pada remaja, 4) tersedia full teks, original artikel dan dapat diakses. Pada metode ini menggunakan framework yang dikembangkan oleh Arksey dn O’Malley dengan beberapa tapahan yaitu: 1. Mengidentifikasi pertanyaan penelitian; 2. Mengidentifikasi study yang relevan; 3. Melakukan seleksi artikel penelitian; 4. Melakukan charting data; 5. Selanjutnya menyusun, meringkas dan melaporkan hasil dari literatur yang didapat sejumlah 11 artikel dari 213 artikel yang didapat. Berdasarkan artikel yang didapatkan, peneliti mengklasifikasikan dampak social jetlag pada kesehatan remaja dalam 2 aspek yaitu aspek fisik seperti obesitas, ganguan metabolik dan kardiovaskuler. Serta gangguan dan psikologis seperti kecemasan, keadaan suasana hati yang negatif serta ketahan yang lebih rendah. Social jetlag berdampak pada seluruh aspek dalam proses perkembangan remaja.
The Impact of Chronotype on Adolescent Health and Behavior: A Scoping Review Rohman, Atiqur; Nur Setiawati Dewi; Meira Erawati
Dunia Keperawatan: Jurnal Keperawatan dan Kesehatan Vol 12 No 2 (2024): Dunia Keperawatan: Jurnal Keperawatan dan Kesehatan
Publisher : School of Nursing, Faculty of Medicine and Health Science, Universitas Lambung Mangkurat

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.20527/jdk.v12i2.500

Abstract

Adolescents exhibit varying sleep-wake behaviors influenced by a range of biological, social, and psychological characteristics. Many adolescents today tend to follow an evening chronotype, which has implications for their health and developmental processes. To date, there has been no specific review synthesizing evidence from studies on the health and behavioral risks associated with chronotype in adolescents. This study aims to identify recent evidence on the health and behavioral impacts of chronotype in adolescents. A scoping review approach was used. Literature sources were obtained through database searches including PUBMED, ScienceDirect, and Scopus. The inclusion criteria for article selection were: (1) articles published within the last 5 years; (2) written in English; (3) article topics related to the impact of chronotype on adolescents; and (4) full-text availability, original articles, and accessible sources. This study employed the framework developed by Arksey and O’Malley, consisting of the following steps: 1. Identifying the research question; 2. Identifying relevant studies; 3. Selecting research articles; 4. Charting the data; and 5. Collating, summarizing, and reporting the results. Based on the selected articles, the researchers classified the impacts of chronotype on adolescent health into three main aspects: physical, psychological, and health-related and social behaviors. Chronotype affects all dimensions of adolescent developmental processes.