# Frailty and disability among older adults residing in Rohingya refugee camp in Bangladesh

**Authors:** Afsana Anwar, Mahmood Parvez, Farhan Azim, Uday Narayan Yadav, Saruna Ghimire, Ateeb Ahmad Parray, Shovon Bhattacharjee, ARM Mehrab Ali, Rashidul Alam Mahumud, Md Irteja Islam, Md Nazmul Huda, Mohammad Enamul Hoque, Probal Kumar Mondal, Abu Ansar Md Rizwan, Suvasish Das Shuvo, Sabuj Kanti Mistry

PMC · DOI: 10.1371/journal.pone.0341499 · PLOS One · 2026-01-23

## TL;DR

This study examines frailty and disability among older Rohingya refugees in Bangladesh, finding high prevalence linked to age, gender, education, and health conditions.

## Contribution

The study identifies key risk factors for frailty and disability in a vulnerable refugee population using multinomial logistic regression.

## Key findings

- Frailty and disability prevalence were 36.92% and 55.21% respectively among Rohingya older adults.
- Older age, being female, lack of education, and non-communicable diseases significantly increased disability risk.
- Frailty was strongly associated with female gender, non-communicable diseases, and loneliness.

## Abstract

Frailty and disability often emerge with ageing and affect quality of life. Older adults residing in Rohingya refugee camp in Bangladesh are particularly susceptible to frailty and disability due to adverse physical and social environment along with limited health and social care services available in the camp. This study aimed to investigate the prevalence and factors associated with frailty and disability among Rohingya older adults living in Bangladesh.

This cross-sectional study was conducted among older adults aged ≥60 years residing in the Rohingya refugee settlement in Bangladesh. The primary outcomes were frailty and disability, explored using the ‘Frail Non-Disabled (FiND) questionnaire. Data were collected face-to-face during November-December 2021, using a semi-structured questionnaire. A multinomial logistic regression model was used to identify the factors associated with frailty and disability.

The majority of participants (n = 864) were aged 60–69 years (72.34%), male (56.25%), married (79.05%), and without formal education (89.0%). The study revealed a high prevalence of frailty (36.92%) and disability (55.21%) among the participants. The multinomial regression analysis showed that the likelihood of experiencing disability was significantly higher among participants who were aged 70–79 years (RRR = 2.65, 95% CI: 1.25, 5.66) and ≥80 years (RRR = 8.06, 95% CI: 1.05, 61.80), were female (RRR = 3.93, 95% CI: 1.88, 8.1.9), had no formal education (RRR = 4.34, 95% CI: 2.19, 8.63), were living in a large family (RRR = 1.82, 95% CI: 1.05, 3.18) and were suffering from non-communicable diseases (RRR = 2.36, 95% CI: 1.32, 4.22) compared to their respective counterparts. The regression analysis also revealed that frailty was significantly higher among participants who were female (RRR = 2.82, 95% CI: 1.34, 5.94), were suffering from non-communicable diseases (RRR = 2.28, 95% CI: 1.27, 4.09), and had feeling of loneliness (RRR = 2.16, 95% CI: 1.11, 4.22).

The findings underscore the need for long-term care and health promotion activities to alleviate the burden of frailty and disability among older adults in humanitarian settings. Efforts should particularly target the most vulnerable groups- older individuals (≥80 years), women, those without formal education, those living in large families, and those with non-communicable diseases.

## Full-text entities

- **Diseases:** dementia (MESH:D003704), Disability (MESH:D009069), communicable diseases (MESH:D003141), cancer (MESH:D009369), human rights violations (MESH:C535682), schizophrenia (MESH:D012559), FiND (MESH:D000073496), infection (MESH:D007239), slow gait speed (MESH:D020234), stroke (MESH:D020521), concentration problems (MESH:C567712), hypertension (MESH:D006973), chronic kidney disease (MESH:D051436), arthritis (MESH:D001168), hypercholesterolemia (MESH:D006937), heart disease (MESH:D006331), diabetes (MESH:D003920), Non (MESH:C580335), non-communicable diseases (MESH:D000073296), weakness (MESH:D018908), cognitive decline (MESH:D003072), bipolar mood disorder (MESH:D001714), geriatric malnutrition (MESH:D044342), chronic respiratory diseases (MESH:D012140), weight loss (MESH:D015431), inactivity (MESH:C564765), functional disabilities (MESH:D003291)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

85 references — full list in the complete paper: https://tomesphere.com/paper/PMC12829860/full.md

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Source: https://tomesphere.com/paper/PMC12829860