Copenhagen University Hospital, Amager
Copenhagen, 2300, Denmark
NCT Number: NCT06242301
The aim of this mixed methods trial is to investigate the feasibility of a collective person-centred dialogue (COPE-D) intervention delivered by an interdisciplinary team for a population of patients hospitalised and diagnosed with COPD and their relatives.
The main questions it aims to answer are:
* The clinical uncertainties: What components of the COPE-D intervention are delivered to the included patients? (The data will be collected from the patient's journal record) * The clinical uncertainties: How acceptable is the COPE-D intervention for the patients, relatives, and the interdisciplinary team? (Answered by patient and relative interviews with a structured interview guide before discharge and 14 days after hospitalisation, and by the interdisciplinary team using focus-group interviews after the intervention enrolment). * The procedural uncertainties: Are the patients willing to engage in the trial? (Estimated by the inclusion rate).
The interdisciplinary team will be instructed to deliver and document the COPE-D intervention. The primary focus of COPE-D intervention is to prepare and enhance the patient's and relative's ability to regain their everyday life after discharge. The COPE-D intervention includes a dialogue tool based on a needs assessment, an action plan template, and a patient guide that prepares for discharge.
The interdisciplinary team will collaborate with COPD patients and their relatives to:
1. Assess the patient's need for nutrition and physical activity support, both during and after hospitalisation using the dialogue tool. 2. Develop an action plan for nutrition and physical activity support using the action plan template. 3. The interdisciplinary team will provide, adjust, and document the nutritional and physical activity support provided by the action plan. 4. Prior to discharge, patients and their relatives are given a discharge guide with pre-defined questions to ask healthcare professionals, a contact telephone number to the outpatient clinic for follow-up if needed, and information about prescriptions for oral nutritional supplementation.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Copenhagen, 2300, Denmark
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: Measurements will be taken at one time point for each participant prior to discharge. Measurements will be taken four weeks after the beginning of the intervention.
Following criteria are considered to evaluate the delivery of the needs assessment and the action plan:
Time frame: Measurements will be taken at one time point for each participant prior to discharge. Measurements will be taken four weeks after the beginning of the intervention.
Following criteria are considered to evaluate the delivery of the provision actions from the action plan:
The modification of the intervention will be based on the completed feasibility test.
Time frame: Measurements will be taken at one time point for each participant prior to discharge. Measurements will be taken four weeks after the beginning of the intervention.
Following criteria are considered to evaluate the patients and their relative acceptability of the intervention.
Any decision to modify the intervention will be based on the completed analysis of the feasibility.
Time frame: The measurement will be assessed after the intervention at week six
The assessment will be measured qualitatively. Focus group interviews will be conducted using a semi-structured interview guide.
Time frame: .Measurement will be taken during recruitment. Measurements will be taken four weeks after the beginning of the intervention.
Following criteria are considered to evaluate the recruitment for paricipation in the intervention:
Determine contextual factors that may influence the recruitment process. Discuss in the focus group interviews with the interdisciplinary team and with the department managers about potential contextual factors that may influence the low recruitment rate.
Hvidovre University Hospital
Other
Feasibility Assessment of a Collective Person-centered Dialogue (COPE-D) Intervention for Patients Hospitalised with COPD Exacerbation
Acronym: COPE-D
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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