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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02274701
Other study ID # 14/WS/0126
Secondary ID
Status Not yet recruiting
Phase N/A
First received October 16, 2014
Last updated October 24, 2014
Start date October 2014
Est. completion date February 2016

Study information

Verified date October 2014
Source University of the West of Scotland
Contact Austyn Snowden
Email Austyn.Snowden@uws.ac.uk
Is FDA regulated No
Health authority United Kingdom: National Health Service
Study type Interventional

Clinical Trial 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.


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 information / eligibility

Status Not yet recruiting
Enrollment 156
Est. completion date February 2016
Est. primary completion date October 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility 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

Allocation: Randomized, Intervention Model: Parallel Assignment, Primary Purpose: Supportive Care


Related Conditions & MeSH terms

  • Oncology [See Also, Affected System]

Intervention

Other:
Holistic Needs Assessment
An assessment completed by the patient in cancer care. It is recommended that this assessment is completed at key points in the care pathway, such as at diagnosis, post treatment and beginning of end of life care. The aim of this assessment is to allow the patient to discuss their most important needs as identified by them. The clinician will take any appropriate action. This may range from listening to the patient to referring to another member of the multi-disciplinary team.

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
University of the West of Scotland Macmillan Cancer Support

References & Publications (2)

Snowden A, White CA, Christie Z, Murray E, McGowan C, Scott R. Helping the clinician help me: towards listening in cancer care. Br J Nurs. 2012 May 24-Jun 13;21(10):S18, S20-6. — View Citation

Snowden A, White CA, Christie Z, Murray E, McGowan C, Scott R. The clinical utility of the distress thermometer: a review. Br J Nurs. 2011 Feb 24-Mar 9;20(4):220-7. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Patient participation 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. This outcome measure will be collected during the patients first clinic appointment after treatment for their cancer. The consultation will last approximately 15 minutes. No
Secondary Shared decision making 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. This 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. No
Secondary Self-efficacy Measured through self-report using The Lorig Self-Efficacy for Managing Chronic Disease 6-Item Scale. This 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.. No
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