Chittagong Medical College Hospital
Chittagong, Bangladesh
NCT Number: NCT07232901
The goal of this trial is to evaluate whether a family participation training intervention can reduce caregiver strain and health worker workload, and improve patient outcomes and collaboration in the medicine wards of Chittagong Medical College Hospital (CMCH).
General objectives:
* To assess the effect of a family participation training intervention on the medicine wards of CMCH. (Stepped-wedge) * To examine how, for whom and under what circumstances a family participation training intervention works. (Realist evaluation)
Specific objectives:
* To examine the implementation of a family participation training intervention. * To investigate the acceptability and feasibility of a family participation training intervention.
The study will use a step-by-step roll-out, introducing training at different times in three wards, to see if it improves care compared to usual practice.
Study participants will include adult patients, their family caregivers, nurses, doctors, ward assistants, and hospital administrators. Health workers will be trained to deliver sessions to family caregivers of hospitalised patients on hospital introduction, basic care tasks, warning sign detection, oral medication administration, caregiver handover, and discharge preparedness.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Chittagong, Bangladesh
Background:
In many resource-limited settings, understaffed hospitals rely on the families of patients to provide care during admission. Family participation in hospital care may include washing, toileting, feeding, administering medication, and detecting warning signs. Family participation in hospital care is commonplace at Chittagong Medical College Hospital (CMCH) and other hospitals in Bangladesh. These care tasks are often performed informally, untrained, and unsupported, resulting in a high mental and physical burden of care for family caregivers, unknown effects on patient outcomes and potentially an even higher workload for health workers. This study proposes to implement and evaluate a family participation training intervention in the general medicine wards of CMCH. Building on prior preparatory research, the intervention aims to reduce family caregiver strain, lower health workers' workloads, enhance patient outcomes and improve collaboration between family caregivers and health workers.
Objective The primary objectives of the study are to assess the effect of a family participation training intervention on the medicine wards of CMCH and to examine how, for whom and under what circumstances a family participation training intervention works.
Methods The study employs a stepped-wedge realist trial over six months in the CMCH medicine wards (13, 14, and 16). It involves adult patients, family caregivers, health workers (nurses, doctors, and ward assistants), and hospital administrators. Family caregivers will receive training to support their participation in hospital care, while nurses and doctors will be trained to deliver these sessions. The training will include an introduction to the hospital, basic hospital care, oral medication administration, detection of warning signs, handover between family caregivers, and discharge preparation. The primary outcomes are reduced family caregiver strain and lower health worker workload. Patient-family caregiver dyads will be followed daily for up to five days during admission and one call after discharge. Health workers will be followed throughout the study period. In addition, ward-level, implementation, feasibility, and acceptability outcomes will be collected. Some patients, family caregivers, health workers, and hospital administrators will be included in realist interviews or focus group discussions. The analysis will integrate mixed-effects modelling with a realist evaluation approach.
Discussion This study will add a foundational piece of research to the family participation field, in resource-limited and -rich settings. It builds on the shared journey of this growing international research collaboration. No such previous research has been performed. It will be the first to test a co-created family participation training intervention in hospital care. In addition, it suggests new research methods by integrating a stepped-wedge design with a realist evaluation.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
All study parts
Population
Adult
Data collection specific Patient and family caregiver data collection - Patient & family caregiver dyad: admitted for ≤24 hours on the medicine wards
Health worker data collection
Interviews, focus group discussions and observations
During the intervention period
Exclusion criteria
All
Language - Unable to speak Bengali, Chittagonian or English
Consent
Data collection specific Patient and family caregiver data collection
This study will test a family participation training intervention. Family caregivers will receive training on participating in hospital care while nurses and doctors receive training to train family caregivers. The family caregiver training sessions will be delivered during the intervention period in three wards to all family caregivers willing to attend the training session. The intervention has been co-created and piloted with patients, family caregivers, health workers, and hospital administrators. The content of the training will include an introduction to the hospital environment, basic care tasks, warning sign detection, oral medication administration, caregiver handover, and discharge preparedness. The content of the family caregiver training will be bundled in a visual poster. These posters will be hung on the walls across the medicine wards at the patients' bedsides.
Time frame: During 5 day hospital follow-up
Measured with Care-related Quality of Life (CarerQOL), ranging from 0 (worst care situation) to 100 (best care situation)
Time frame: Assessed from inclusion till study end for at least once per study period across four periods, spanning five months in total
Nasa Task Load Index, ranging from 0 (low workload) to 10 (high workload)
Time frame: Continuous refinement from start of the intervention till end of the study, spanning four months in total
The refined programme theories will be developed through iterative analysis of qualitative and quantitative data, outlining what works in the intervention, for whom, and under what circumstances.
Time frame: During 5 day hospital follow-up
Nasa Task Load Index, ranging from 0 (low workload) to 10 (high workload)
Time frame: During 5 day hospital follow-up
Daily collection of which caregiving tasks were performed in the past 24 hours by the main family caregiver, other family caregivers and the patient themselves.
Time frame: During 5 day hospital follow-up
The caregiver is asked daily how ready they would be to provide care at home if their relative would be discharged today.
Time frame: During 5 day hospital follow-up and at 14 day call
Adapted and shortened HCAHPS (Hospital Consumer Assessment of Healthcare Providers and Systems) Survey, measured on a four and ten point scale
Time frame: Assessed from inclusion till study end for at least once per study period across four periods, spanning five months in total
Using the Families' Importance in Nursing Care - Nurses' Attitudes (FINC-NA), measured on a five point scale
Time frame: Assessed from inclusion till study end for at least once per study period across four periods, spanning five months in total
Health workers are asked about their perceived increase or decrease in interruptions during work by family caregivers
Time frame: During 5 day hospital follow-up
Adapted and shortened HCAHPS (Hospital Consumer Assessment of Healthcare Providers and Systems) Survey, measured on a four and ten point scale
Time frame: During 5 day hospital follow-up
Patient Health Questionnaire-4 (PHQ-4), measured on a four point scale
Time frame: During 5 day hospital follow-up
Patient Readiness for Discharge Scale, measured from 0 (worst) to 10 (best) readiness
Time frame: During 5 day hospital follow-up
Pill counts
Time frame: During 5 day hospital follow-up and 14 day call
Outcome of hospital admission: discharged home alive, left against medical advice, in another hospital, died in hospital, discharged home to die, in ICU, in another ward, still in the medicine ward, lost to follow-up.
Time frame: Continuous data collection from the start of the intervention until the end of the study (four months in total).
Training logs recording all family caregivers and patients trained
Time frame: Continuous data collection from the start of the intervention until the end of the study (four months in total).
Uptake of the intervention by health workers and the ward.
Time frame: Continuous data collection from the start of the intervention until the end of the study (four months in total).
Fidelity sheets of the training sessions
Time frame: Continuous data collection from the start of the intervention until the end of the study (four months in total).
Modifications made during implementation of the intervention
Time frame: Continuous data collection from the start of the intervention until the end of the study (four months in total).
Resources required to deliver the intervention
Time frame: Continuous data collection from the start of the intervention until the end of the study (four months in total).
Qualitative assessment of integration of the training intervention into the health worker and ward workflow, resource feasibility of the intervention, buy-in from stakeholders and feasibility of the research methods for this intervention type.
Michele van Vugt
Other
Implementing Family Participation Training in Tertiary Hospital Care in Bangladesh: a Stepped-wedge Realist Trial
Acronym: FAMCARE
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