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Frailty Syndrome and Its Associated Factors Among Elderly Patients (Frailty)

21 de julho de 2026 atualizado por: Asma Ahmed Rafat Najeeb, Assiut University

Frailty Syndrome and Its Associated Factors Among Elderly Patients Attending Assiut University Hospitals

This is a cross-sectional analytical study conducted among elderly patients attending Assiut university hospital.

2.4. 2- Study Setting:The study will be conducted in Assiut University hospital, including outpatients and inpatients who fulfill inclusion criteria.

2.4. 3- Study subjects:

  • a. Inclusion criteria:
  • Age ≥ 60 years
  • Patient attending Assiut university hospital during the study period, regardless primary diagnosis.
  • Ability to provide informed consent and agreed to participate in the study.
  • Ability to communicate and answer the study questionnaire.
  • b. Exclusion criteria:
  • Age < 60 years
  • Patients admitted for elective surgical procedures or transferred from surgical wards
  • Patients with a terminal illness or those receiving palliative/end-of-life care only
  • Patients with incomplete medical records or inability to complete the assessment due to severe aphasia or critical hemodynamic instability
  • Patients with severe cognitive impairment or psychiatric disorders affecting communication.
  • Patients who refused to participate

    c. Sample Size Calculation: Based on determining the main outcome variable, the estimated minimum required sample size is 175 patients.

The sample size was calculated using Epi-Info version 7 software, based on the following assumptions:

Based on a previous study by Perez-Zepeda et al. (2023)(3), which reported a frailty prevalence of approximately 42% among hospitalized elderly patients using the Frailty Index with a deficit accumulation approach, Based on a confidence level of 90% and an absolute precision (confidence limit) of 5%.

2.4.4 Study tools:

The study will be done by using a semi structured questionnaire that will include four sections as follows:

Section I: Sociodemographic and Clinical Data Sheet:

A structured interviewer-administered data collection form will be used to record baseline sociodemographic and clinical characteristics of all enrolled patients. This will include age, sex, level of education, marital status, and place of residence. Clinical data will encompass the primary diagnosis on admission, all documented comorbidities, total number of regular medications (polypharmacy defined as the concurrent use of five or more medications), smoking history, and the number of hospital admissions within the preceding 12 months.

Section II: The 30-Item Frailty Index (FI):

Frailty will be assessed using a 30-item Frailty Index (FI) constructed in accordance with the deficit accumulation model originally proposed by Rockwood and Mitnitski. This model conceptualizes frailty as the cumulative burden of age-related health deficits across multiple physiological domains. Each deficit is coded as 0 (absent) or 1 (present); where a deficit is gradable in severity, an intermediate score of 0.5 is assigned. The FI is calculated by the following formula:

FI="Number of deficits present" /30

Participants are subsequently classified into three frailty categories according to their FI score:

FI Score Frailty Category < 0.10 Robust 0.10 - 0.24 Pre-frail

≥ 0.25 Frail

Section III. Physical examination and Anthropometric Measurements:

All participants will undergo a comprehensive physical examination including assessment of vital signs (blood pressure, pulse rate, respiratory rate, and body temperature), anthropometric measurements (weight, height and body mass index), and a systematic clinical examination relevant to the study objectives.

  • Body weight will be measured using calibrated digital scales, with the patient wearing light clothing and no shoes
  • Height will be measured using a wall-mounted stadiometer
  • BMI will be calculated accordingly Findings will be recorded in a standardized data collection sheet.

Section IV. Laboratory Investigations:

The following investigations will be collected from the routine admission workup or ordered as part of the study protocol:

  • Complete blood count (CBC) for hemoglobin and hematocrit
  • Serum albumin measured by colorimetric bromocresol green (BCG) method
  • Random blood glucose for diabetes assessment

Visão geral do estudo

Status

Ainda não está recrutando

Descrição detalhada

The 30-Item Frailty Index (FI):

Frailty will be assessed using a 30-item Frailty Index (FI) constructed in accordance with the deficit accumulation model originally proposed by Rockwood and Mitnitski. This model conceptualizes frailty as the cumulative burden of age-related health deficits across multiple physiological domains. Each deficit is coded as 0 (absent) or 1 (present); where a deficit is gradable in severity, an intermediate score of 0.5 is assigned. The FI is calculated by the following formula:

FI="Number of deficits present" /30

Participants are subsequently classified into three frailty categories according to their FI score:

FI Score Frailty Category < 0.10 Robust 0.10 - 0.24 Pre-frail

≥ 0.25 Frail

The 30 deficits are distributed across six sections as follows:

Section A: Chronic Diseases (10 items) The presence of each chronic disease is confirmed through a combination of patient interview, review of medical records, and available investigation results. The ten items are: hypertension (diagnosed and/or on antihypertensive therapy); diabetes mellitus (diagnosed and/or on antidiabetic treatment); ischemic heart disease (confirmed by electrocardiography, echocardiography, or documented medical history); heart failure (diagnosed clinically and/or by echocardiographic assessment of ejection fraction); atrial fibrillation (confirmed on 12-lead ECG or Holter monitoring); prior stroke or transient ischemic attack (documented cerebrovascular event in the medical record); chronic obstructive pulmonary disease or chronic lung disease (diagnosed by spirometry or clinical assessment); chronic kidney disease (estimated glomerular filtration rate below 60 mL/min/1.73m² for more than three months); chronic liver disease (confirmed by clinical, laboratory, or imaging findings); and active or prior malignancy (confirmed by histopathological report or documented in the clinical record).

Section B: General Symptoms (5 items):

These items are assessed through a structured patient interview. They include: unintentional weight loss, defined as a loss of more than 4.5 kg or more than 5% of body weight over the preceding year; persistent fatigue, defined as self-reported fatigue present most of the time for a duration of three or more months; chronic pain, defined as pain persisting beyond three months and requiring regular analgesia or limiting daily activity; dyspnea on exertion, graded using the Modified Medical Research Council (mMRC) Dyspnea Scale with a score of 2 or above considered positive; and poor appetite, defined as self-reported reduction in food intake over the preceding month.

Section C: Basic Activities of Daily Living - ADL (5 items):

Functional status with respect to basic self-care activities will be assessed using the Katz Activities of Daily Living (ADL) Scale. Dependency in any of the following activities will be coded as 1 (dependent) versus 0 (independent): bathing, dressing, toileting, transferring from bed to chair, and feeding. Pre-admission functional status will be recorded based on patient or caregiver recall to reflect the patient's baseline prior to the acute illness.

Section D: Instrumental Activities of Daily Living - IADL (4 items):

Higher-order functional independence will be assessed using the Lawton Instrumental Activities of Daily Living (IADL) Scale. The four items assessed are: ability to use a telephone, ability to shop, ability to prepare meals, and ability to manage medications. Each item is coded as 0 (independent) or 1 (dependent).

Section E: Cognition and Mood (3 items):

Cognitive status will be evaluated using the Mini-Mental State Examination (MMSE); a score below 24 will be coded as cognitive impairment (1). Depressive symptoms will be screened using the 15-item Geriatric Depression Scale (GDS-15); a score of 6 or above will be coded as depression (1). Subjective memory complaint, defined as self-reported difficulty with memory not fully captured by formal cognitive testing, will be recorded separately and coded as 0 (absent) or 1 (present).

Section F: Physical and Laboratory Indicators (3 items):

Three objectively measured indicators will be included. Anemia is defined according to World Health Organization (WHO) criteria as a hemoglobin level below 13 g/dL in men and below 12 g/dL in women, determined from the admission complete blood count. Hypoalbuminemia is defined as a serum albumin level below 3.5 g/dL, measured using the colorimetric bromocresol green (BCG) method on the admission blood sample. Abnormal body mass index (BMI) is defined as BMI below 18.5 kg/m² (underweight) or 30 kg/m² and above (obese); body weight will be measured using a calibrated digital scale with the patient in light clothing and without footwear, and height will be measured using a wall-mounted stadiometer.

Tipo de estudo

Observacional

Inscrição (Estimado)

175

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

  • Nome: Asma Ahmed Rafat, specialist
  • Número de telefone: +201030533071
  • E-mail: asmaacc@yahoo.com

Estude backup de contato

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Método de amostragem

Amostra Não Probabilística

População do estudo

elderly patients attending Assiut university hospital, including outpatients and inpatients who fulfill inclusion criteria.

Descrição

  • a. Inclusion criteria:
  • Age ≥ 60 years
  • Patient attending Assiut university hospital during the study period, regardless primary diagnosis.
  • Ability to provide informed consent and agreed to participate in the study.
  • Ability to communicate and answer the study questionnaire.
  • b. Exclusion criteria:
  • Age < 60 years
  • Patients admitted for elective surgical procedures or transferred from surgical wards
  • Patients with a terminal illness or those receiving palliative/end-of-life care only
  • Patients with incomplete medical records or inability to complete the assessment due to severe aphasia or critical hemodynamic instability
  • Patients with severe cognitive impairment or psychiatric disorders affecting communication.
  • Patients who refused to participate

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

Coortes e Intervenções

Grupo / Coorte
• Patient attending Assiut university hospital during the study period aged above 60 years
  • a. Inclusion criteria:
  • Age ≥ 60 years
  • Patient attending Assiut university hospital during the study period, regardless primary diagnosis.
  • Ability to provide informed consent and agreed to participate in the study.
  • Ability to communicate and answer the study questionnaire.
  • b. Exclusion criteria:
  • Age < 60 years
  • Patients admitted for elective surgical procedures or transferred from surgical wards
  • Patients with a terminal illness or those receiving palliative/end-of-life care only
  • Patients with incomplete medical records or inability to complete the assessment due to severe aphasia or critical hemodynamic instability
  • Patients with severe cognitive impairment or psychiatric disorders affecting communication.
  • Patients who refused to participate

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
• Prevalence of frailty syndrome
Prazo: Baseline
• Prevalence of frailty syndrome among elderly patients attending Assiut university hospital, defined as FI ≥ 0.25
Baseline

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Socio-demographic characteristics associated with frailty syndrome
Prazo: Baseline
Assessment of age, gender, education level, living arrangement, and marital status collected via a structured questionnaire
Baseline

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Patrocinador

Investigadores

  • Diretor de estudo: Dalia Galal Mahran, professor, Professor at Public Health and community medicine Department, Head of Family medicine department

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

20 de julho de 2026

Conclusão Primária (Estimado)

20 de julho de 2027

Conclusão do estudo (Estimado)

20 de julho de 2027

Datas de inscrição no estudo

Enviado pela primeira vez

2 de julho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

21 de julho de 2026

Primeira postagem (Real)

27 de julho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

27 de julho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

21 de julho de 2026

Última verificação

1 de julho de 2026

Mais Informações

Termos relacionados a este estudo

Palavras-chave

Outros números de identificação do estudo

  • Frailty Syndrome

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

INDECISO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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