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Holistic Needs Assessment in Outpatient Cancer Care

Not Applicable
Conditions
Oncology [See Also, Affected System]
Interventions
Other: Holistic Needs Assessment
Registration Number
NCT02274701
Lead Sponsor
University of the West of Scotland
Brief Summary

This study evaluates the impact of holistic needs assessment (HNA) on patient/clinician communication in outpatient cancer care. Half of the participants will complete a HNA prior to their clinical consultation. They will then take it into the consultation and it will inform a discussion around any identified areas of need. Half of the participants will be in the control group meaning there will be no additional intervention they will receive care as normal. The consultations will be audio-recorded. The patient will complete two outcome measures following the consultation.

Detailed Description

Holistic needs assessment is a checklist completed by the patient prior to consultation. It signposts issues of emotional, practical, financial and clinical concern. The purpose of a HNA is to identify patient's individual needs in order to facilitate better collaboration. During consultation the HNA facilitates a dialogue that will have the patient's concerns at the centre. In conjunction with a subsequent care plan the process supports timely intervention based on a collaborative, person centred discussion. However, there is little evidence on how HNA impacts upon the dynamics of the clinical consultation. This study aims to establish a) how HNA affects the type of conversation that goes on during a clinical consultation and b) how these putative changes impact on shared decision-making and self-efficacy.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
156
Inclusion Criteria
  • Over 18, capable of informed consent and expresses a wish to participate.
  • Diagnosed with cancer and attending a post-treatment out-patient oncology clinic.
Exclusion Criteria
  • Individuals not diagnosed with cancer.
  • Non English speaker
  • Person deemed incapable of consenting to participate as defined by the Adults with Incapacity Act (2000)
  • Any reason which in the opinion of the clinician/investigator interferes with the ability of the patient to participate in the study

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Holistic Needs AssessmentHolistic Needs AssessmentParticipants (patients) complete a self-reported paper assessment that asks them to indicate whether they have any emotional, practical, financial and/or clinical concerns. The patient then takes this completed assessment into their consultation. It is then given to the clinician where it informs a discussion based on the patient's needs and concerns as identified by them. A care plan is then written based on this assessment.
Primary Outcome Measures
NameTimeMethod
Patient participationThis outcome measure will be collected during the patients first clinic appointment after treatment for their cancer. The consultation will last approximately 15 minutes.

Measured through analysis of the audio-recordings from each recorded consultation between a clinician and patient. Specifically, through measuring dialogue ratio and preponderance of initiative. These two measures indicate who is speaking, when and for how long.

Secondary Outcome Measures
NameTimeMethod
Shared decision makingThis outcome measure will be collected following the patients first clinic appointment after treatment. The patient will return to the researcher and complete this measure. It is expected to take no more than 1 minute to complete.

Measured through patient self-report using the measure CollaboRATE. CollaboRATE is a survey-based validated tool designed to create a fast way to measure how much effort clinicians make to explain their patients' health issues; how much effort they make to listen to the issues that matter most to their patients and how much effort they make to integrate the patients' views and health beliefs.

Self-efficacyThis outcome measure will be collected following the patients first clinic appointment after treatment. The patient will return to the researcher and complete this measure. It is expected to take no more than 5 minutes..

Measured through self-report using The Lorig Self-Efficacy for Managing Chronic Disease 6-Item Scale.

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