Faculty of Nursing, Khon Kaen University, Muang District, Khon Kaen 40002, Thailand
*Corresponding Author’s Email: khanitta@kku.ac.th
Keywords: Community Health Services; Health Service Access; People with Disabilities (PWD); Self-Care; Supportive Systems
Globally, 1.3 billion people (16%) have disabilities, and this number is increasing due to genetic factors, illness, aging, or accidents (WHO, 2022). Disabilities are classified by type in accordance with the International Classification of Functioning, Disability, and Health (ICF). People with disabilities (PWD) face a higher risk of dying up to 20 years earlier than the general population and are more vulnerable to health problems. They encounter up to 15 times more restrictions due to limited healthcare access and financial burdens. Their daily lives are further affected by health inequities, discrimination, stigmatization, poverty, exclusion from education and employment, unmet healthcare needs, and poor- quality care (WHO, 2024; Umucu et al., 2025). Persistent disparities in healthcare access leave many behind, resulting in lower life expectancy, poorer health outcomes, and increased vulnerability during health emergencies (WHO, 2022).
In Thailand, 2.22 million people are living with disabilities (Department of Empowerment of Persons with Disabilities, 2025). The proportion of individuals experiencing severe health difficulties increased from 4.1% in 2017 to 4.7% in 2022. Among them, 2% face significant health issues, live in poverty, and lack educational opportunities (National Statistical Office, 2023). Additionally, many experience domestic or community-based violence, and some have attempted suicide (Seesaet et al., 2020). Thailand has adopted measures to ensure a service package for PWD (Department of Empowerment of Persons with Disabilities, 2023). However, many PWD still face substantial barriers to accessing these services due to personal, financial, attitudinal, communication, and other factors (Said et al., 2024; Phutthisrimethi & Lowatcharin, 2020).
The literature review found that Health Promotion Hospitals play a key role in delivering participatory health services within communities (National Health Security Office, 2024). Local Administrative Organizations (LAO) also contribute to improving residents’ quality of life (Ministry of Interior, 2024), but each organization operates within its own defined roles and responsibilities. Thailand’s healthcare policies aim to ensure equitable access to care, including free medical services and a decentralization policy that transfers the management of Health Promotion Hospitals to provincial administrative organizations to strengthen community-level services. Although various types of health services exist, none are directed specifically toward PWD (Ministry of Public Health, 2025).
Culture significantly influences healthcare practices (Duangwises, 2017), and traditional medicine is widely used for rehabilitation and treatment (Department of Medical Services, Ministry of Public Health, 2020). The role of culture is essential in shaping the effectiveness and accessibility of health services for PWD (Hashemi et al., 2022). However, traditional beliefs about illness and the importance of spiritual healing may lead some PWD and their families to delay or avoid seeking formal health services (Pavasuthipaisit et al., 2018).
Cultural stigma surrounding disability can further discourage individuals from utilizing formal care. In addition, family-centered caregiving—a hallmark of Thai culture—while offering emotional support, may inadvertently limit engagement with structured healthcare systems. However, gaps remain in the comprehensive understanding and integration of these practices within the formal healthcare system. This indicates a critical research gap in developing a model that integrates health services. Existing studies provide limited insight into how health services are specifically delivered to PWD. Nurses play a central role in bridging these gaps by coordinating community resources, health services, and relevant policies (Nursing Council of Thailand, 2005).
The complexity of this issue, shaped by social and cultural contexts, aligns with Postmodernist philosophy, which emphasizes interpreting phenomena within their lived environments. Ethnographic research, rooted in anthropology, is designed to examine and understand behaviors within their sociocultural context (Alotaibi, 2018; Creswell & Poth, 2007). It is effective in capturing patient experiences and informing the development of nursing knowledge (Strudwick, 2020). Therefore, an ethnographic qualitative approach can identify disparities and guide improvements in community health services for PWD. This study aims to explore these services to address existing service gaps and contribute to a more inclusive community health system for PWD.
This study employed an ethnographic approach to explore the research phenomenon in depth (Hardcastle et al., 2006). The Consolidated Criteria for Reporting Qualitative Research (COREQ) guidelines were followed to ensure methodological rigor and transparency throughout the study (Tong et al., 2007).
The study was conducted in a sub-district in northern Thailand, consisting of 12 villages with a total population of 9,384, including 344 individuals with disabilities (3.66%). Most residents work in agriculture, and the primary languages spoken are Lao Wiang and Thai. The community has strong social capital, supported by more than one hundred community-based resources and participatory activities that help reduce health disparities within the local context.
A total of 65 participants were selected through purposive sampling based on their experience in providing health services, including PWD, family members, healthcare providers, community leaders, LAO officers, volunteers, neighbors, and relatives. Recruitment continued until data saturation was reached. Inclusion criteria required participants to have experience in delivering health services for PWD and to have the ability to communicate. Participants were informed of their right to withdraw from the study at any time, particularly if they felt unwell or unable to continue.
After receiving approval from the Institutional Review Board, data were collected over a 13-month period (July 2023–August 2024). A data collection guideline was developed to ensure consistency throughout the process. Access to data sources was facilitated by a community gatekeeper.
The researcher encompassed both etic and emic perspectives in accordance with the ethnographic method used to comprehensively investigate the values, beliefs, and cultural practices of PWD. The study utilized an ethnographic approach to data collection (Hardcastle et al., 2006).
The study utilized an ethnographic approach (Hardcastle et al., 2006). Thematic analysis was conducted following the framework proposed by Braun and Clarke (Braun & Clarke, 2006). Interviews were transcribed verbatim and reviewed multiple times to ensure familiarity with the content. Data were coded, and similar codes were grouped into categories. Subcategories were refined and merged into broader themes representing participants lived experiences with community health services for PWD. To enhance accuracy and credibility, themes were cross validated by comparing data from interviews, observations, and documents. Findings were confirmed through member checking with local informants and reviewed in consultation with a research advisor.
To ensure rigor throughout the research process, the study strictly adhered to four criteria for trustworthiness: credibility, transferability, dependability, and confirmability (Ahmed, 2024). Credibility was established through prolonged engagement in community activities, persistent observation, and triangulation of data sources (interviews, observations, and documents). Transferability was supported by providing detailed descriptions of participant selection, including participant types and demographic characteristics, allowing the findings to be applied to similar contexts. Dependability was maintained by using multiple data collection methods and clearly outlining the research questions, procedures, and participant details to ensure transparency. Confirmability was achieved through informant feedback, field notes, and expert consultation, helping to minimize potential researcher bias.
This research received ethical approval from the Human Research Ethics Committee of Khon Kaen University, Thailand, with reference number HE662114 on 23rd June, 2023.
Throughout this study, data was collected from 65 informants who had experience in providing health services. The characteristics of the participants are shown in Table 1.
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Table 1: Characteristics of the Participants (N=65)
Participants | Code | Characteristics | Quantity |
PWD (n=19) | P1-19 | Age | X = 54.52 (SD = 22.66) |
Sex | |||
Male | 9 (47.36%) | ||
Female | 10 (52.63%) | ||
Living | |||
Alone | 6 (31.57%) | ||
Family | 13 (68.42%) | ||
Income (THB/month) | X = 1.716 (SD = 2,149) | ||
Education | |||
No formal education | 10 (52.63%) | ||
Primary school | 6 (31.58%) | ||
High-school | 3 (15.79%) | ||
ADL (Activities of Daily Life) | |||
0-4 (total-dependence) | 5 (26.32%) | ||
5-11(moderately-dependence) | 2 (10.53%) | ||
≥12 (independence) | 12 (63.16%) | ||
Disease | |||
No underlying disease | 9 (47.37%) | ||
Hypertension | 6 (31.58%) | ||
Colon cancer (CA) | 1 (5.26%) | ||
HIV+ | 2 (10.53%) | ||
Seize | 1 (5.26%) | ||
Family-Caregiver (n=19) | PF1-19 | Age | X = 54.22 (SD = 12.83) |
Sex | |||
Male | 5 (26.32%) | ||
Female | 14 (73.68%) | ||
Income | X = 7.379 (SD = 5,446) | ||
Volunteers (n=9) | PV1-9 | Age | X = 59.36 (SD = 13.57) |
Sex | |||
Male | 2 (22.22%) | ||
Female | 7 (77.78%) | ||
Healthcare providers (n=6) | PP1-6 | Age | X = 38.16 (SD = 9.32) |
Professional Roles of Healthcare Providers | |||
PP1-2 | Nurse | 2 (33.33%) | |
PP3 | Public-health officers | 1 (16.67%) | |
PP4 | Dentist | 1 (16.67%) | |
PP5 | Director | 1 (16.67%) | |
PP6 | Physiotherapist | 1 (16.67%) | |
LAO and Leaders (n=5) | PO1-5 | Age | X =53 (SD = 4.14) |
Leadership and Administrative Positions | |||
PO1 | Head of LAO | 1 (20.00%) | |
PO2-3 | Director of division | 2 (40.00%) | |
PO4 | Officer | 1 (20.00%) | |
PO5 | Head of community | 1 (20.00%) | |
Related people (n=7) | PG1-7 | Age | X =55.9 (SD = 18.07) |
Community Representatives | |||
PG1-3 | Neighbors | 3 (42.86%) | |
PG4 | Monk | 1 (14.29%) | |
PG5 | Business-owner | 1 (14.29%) | |
PG6 | Teacher | 1 (14.29%) | |
PG7 | Officer | 1 (14.29%) | |
The ethnographic study identified three main themes and 14 sub-themes, highlighting issues related to community health services for PWD (Table 2). The findings are presented in detail, with selected quotes from observations and interviews shown in italics.
Table 2: Thematic Finding
Theme | Sub-themes |
Self-Care System | Belief |
Thai-traditional-medicine | |
Cultural wisdom | |
Health-services-system | Primary care services |
Rehabilitation | |
Emergency medicine and referrals | |
Long-term care (LTC) | |
Palliative-care | |
Thai-traditional-medicine | |
Volunteers | |
Supportive-System | Data-utilization |
Public services | |
Government Welfare | |
Mutual assistance |
“There was a spirit father who performed a ritual by blowing and bathing me with holy water. At that time, I was in pain and had a headache from something unseen. The hospital couldn’t help, so I turned to a healer. If it’s a spirit mother or spirit father, I recover very quickly.” (P10)
“I use turmeric to relieve bloating drying it in the sun, grinding it with lime peel. This recipe was passed down to me. I now teach it at Lamduan Waisai School ( senior school) , where we also make herbal compresses, balms, and inhalers.” (P3)
“My younger brother made a pulley for me to use at work. Sometimes he helps, sometimes he doesn't— but it helps me stay active.” (P4)
“ I joined in playing Mangkala music, which is supported by the Subdistrict Administrative Organization. It’ s a meaningful activity especially for the elderly because it gives us a chance to perform and participate.” (P10)
“...Chronic diseases and common illnesses, like mild sore throats, are managed with medication, often collected by relatives. For blood pressure monitoring, we offer home services, check- ups, in severe cases, referrals are issued, primarily for emergencies requiring further treatment. Every disease follows a Clinical Practice Guideline from the hospital.” (PP1)
“ Rehabilitation programs for PWD are not standardized but are tailored to individual needs, with a strong emphasis on mobility. If patients cannot travel to the hospital, services are provided at the community level, though the frequency varies...” (PP6)
“…He fainted. No one would have noticed at night, but someone saw and called an ambulance to take him to the hospital for treatment.” (P4)
“We raise money to fund projects, buy fuel, provide aid, and keep a reserve fund.” (PO1)
“They come to take care of me—bringing me diapers, cleaning me, and helping with self-care at home. It’ s good. Some use traditional Thai massage and herbal compresses, which make me feel better. ” (P12)
“Cancer patients will receive palliative care. If sent home, a syringe driver is provided, and caregivers manage wound care. In most cases, psychological support is also crucial.” (PP2)
“They teach us how to make compresses and balms, and how to grow and use herbs at home. I soak my feet and apply herbs to my knees.” (P5)
“ Subdistrict Health Promoting Hospital trains us to care for patients, not just those with disabilities but also those needing rehab. I’ve learned a lot and plan to attend more sessions.” (PV4)
“... There is a survey of PWD, but it is not comprehensive. The village community knows who has specific needs, and while we have collected data, it is mainly part of a welfare database. Local records help monitor allowances and support...” (PO2)
“...I get my blood pressure checked regularly. If I need to go to the hospital, I ask my younger brother to notify the Subdistrict Administrative Organization, and they arrange a car for me.” (P7)
“ I receive my disability benefits on time from the Subdistrict Administrative Organization. It really helps—without them, life would be very difficult. I haven’t been able to work since falling ill.” (P4)
“The merit group donated money to help repair houses for PWD, and volunteer technicians also helped with the repairs.” (P6)
Based on the research results, conceptualized the framework of community health services for PWD as presented in Figure 1.
Figure 1: Conceptual Framework of Community Health Services for PWD
The research identified three main themes related to community health services: Self-Care, Health Services, and Support System, which interact with one another (Figure1). Government health services in Thailand provide both reactive and proactive care consistent with public policy frameworks. However, specific programs tailored to the unique needs of PWD are lacking. Although Thailand offers universal health coverage (Ministry of Public Health, 2023; Office of the Decentralization to the Local Government Organization Committee, 2022), it does not include travel costs, accommodation, or essential assistive equipment—barriers that limit actual access to care (Muñoz et al., 2016; Ekakkararungroj et al., 2024). Moreover, healthcare providers often exercise decision-making authority over PWD, such as choosing therapy types or service locations, which further limits autonomy. Therefore, to improve access to health services for PWD, it is necessary to identify individuals and provide care based on their specific problems and needs.
Self-care among PWD reflects a blend of traditional wisdom, spiritual beliefs, and cultural healing practices such as spirit rituals and Thai traditional medicine. While these practices play a valuable role in symptom relief and personal empowerment (Duangwises, 2017), they also present limitations, including slow-acting effects, a lack of formal dosage standards, and limited capacity to treat severe conditions. This imbalance often leads to overreliance on modern medical professionals, who may overlook cultural practices when delivering care (Department of Medical Services, Ministry of Public Health, 2020). To address these issues, nurses play a crucial role as change agents, supporting PWD and caregivers in managing medications, attending appointments, and preventing complications. This approach aligns with Orem’s Self-Care Deficit Nursing Theory, which advocates nurse-led support when individuals are unable to fully care for themselves (Parker & Smith, 2010). However, the shortage of medical personnel remains a challenge for the government sector, though volunteers have been mobilized to help fill this gap.
Improving access to healthcare also requires the strategic use of data systems, public services, and government welfare programs. While data collection is underway in Thailand, it remains fragmented and inconsistent, reducing its effectiveness (Phutthisrimethi & Lowatcharin, 2020). In contrast, countries like Australia have developed national health data systems (e.g., My Health Record) to manage PWD information (Australian Digital Health Agency, 2025). In terms of public services and
welfare, many developed countries apply universal design principles and the welfare state model to ensure comprehensive support for PWD (Gugushvili et al., 2023; European Commission, 2024). Thailand has universal policies, but local infrastructure and budget limitations hinder their implementation. These challenges have led communities to rely on mutual aid efforts, such as fundraising and volunteer networks, to fill service gaps. In response, nurses can foster partnerships with local leaders, government bodies, and civil society organizations to enhance healthcare access. Their role is key in connecting PWD to essential resources such as transportation, financial assistance, and public benefits, thereby ensuring equitable, culturally sensitive, and community-based care (Zulpiani & Rusyani, 2023).
The results highlight that community health services for PWD require the integration of three core components. This model aligns with community- based rehabilitation for older adults’ post- stroke consisting of supportive systems, social and economic support, and administrative and management systems ( Somtua & Nuntaboot, 2025). As supported by systems theory ( Smith- Acuña, 2011), these elements cannot function in isolation but must operate in dynamic interconnection to effectively support vulnerable populations. In alignment with the health commitments of stakeholders for PWD ( International Disability Alliance, 2025) , Thailand has implemented a participatory policy to promote the quality of life for PWD. However, operations remain fragmented; while assistance from the public sector enables implementation at the local level, it is not yet comprehensive.
This study had certain limitations. As it focused on exploring the cultural context of care for PWD within a specific community, the applicability of the findings to other cultural settings requires further investigation.
Community health services for PWD are most effective when built upon the integration of three core components ( figure 1). These components form a comprehensive framework that ensures equitable access to healthcare and promotes the overall well- being of PWD. Effective implementation requires collaboration among key entities: Health Promotion Hospitals, LAOs, community leaders, and etc. Culture need to integrate practices, organizational functions, and community group to ensure the effective and tangible implementation of nursing interventions.
The Implication for nursing practice is to integrate the framework to improve nursing care on culture values. Early intervention and support for PWD should prioritize their culture belief by enhancing specialized healthcare delivery. This includes expanding home- based care, incorporating nursing technologies, and promoting framework with flexible care guidelines tailored to individual needs. For health policy development, there should be collaboration with local governments and community organizations to ensure comprehensive health care. Moreover, local resources should be utilized to ensure the provision of holistic. Further research should focus on developing a culturally adaptive framework of community health services for PWD to enhance nursing care.
The authors declare that there are no conflicts of interest related to this study.
The authors would like to express their heartfelt gratitude to all informants who generously shared their experiences and insights throughout this study.
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