A cluster randomised trial of a Needs Assessment Tool for adult Cancer patients and their carers (NAT-C) in primary care: A feasibility study.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2021
Historique:
received: 19 08 2020
accepted: 05 01 2021
entrez: 28 1 2021
pubmed: 29 1 2021
medline: 16 6 2021
Statut: epublish

Résumé

People with cancer often have unidentified symptoms and social care needs. The Needs Assessment Tool-Cancer (NAT-C) is a validated, structured method of assessing patient/carer concerns and prompting action, to address unmet need. Assess feasibility and acceptability of a definitive two-armed cluster randomised trial of NAT-C in primary care by evaluating: recruitment of GP practices, patients and carers; most effective approach of ensuring NAT-C appointments, acceptability of study measures and follow-up. Non-blinded, feasibility study in four General Practices, with cluster randomisation to method of NAT-C appointment delivery, and process evaluation. Adults with active cancer were invited to participate with or without carer. Practices cluster randomised (1:1) to Arm I: promotion and use of NAT-C with a NAT-C trained clinician or Arm II: clinician of choice irrespective of training status. Participants completed study questionnaires at: baseline, 1, 3 and 6 months. Patients booked a 20 minute needs-assessment appointment post-baseline. Patients, carers and GP practice staff views regarding the study sought through interviews/focus groups. Quantitative data were analysed descriptively. Qualitative data were analysed thematically, informed by Normalisation Process Theory. Progression to a definitive trial was assessed against feasibility outcomes, relating to: recruitment rate, uptake and delivery of the NAT-C, data collection and quality. Five GP practices approached, four recruited and trained to use the NAT-C. Forty-seven participants and 17 carers recruited. At baseline, 34/47 (72%) participants reported at least one moderate-severe unmet need, confirming study rationale. 32/47 (68%) participants received a NAT-C-guided consultation, 19 of which on Arm I. Study attrition at one month (n = 44 (94%), n = 16 (94%)), three months (n = 38 (81%), n = 14 (82%)) and six months (n = 32 (68%), n = 10 (59%)). Fifteen patient interviews conducted across the whole study and one focus group at each GP practice. Participants supported a definitive study and found measures acceptable. The feasibility trial indicated that recruitment rate, intervention uptake and data collection were appropriate, with refinements, for a definitive multi-centre cluster randomised controlled trial. Feasibility outcomes informed the design of a 2-armed cluster randomised controlled trial to test the effectiveness and cost-effectiveness of the NAT-C compared with usual care.

Sections du résumé

BACKGROUND
People with cancer often have unidentified symptoms and social care needs. The Needs Assessment Tool-Cancer (NAT-C) is a validated, structured method of assessing patient/carer concerns and prompting action, to address unmet need.
AIMS
Assess feasibility and acceptability of a definitive two-armed cluster randomised trial of NAT-C in primary care by evaluating: recruitment of GP practices, patients and carers; most effective approach of ensuring NAT-C appointments, acceptability of study measures and follow-up.
METHODS
Non-blinded, feasibility study in four General Practices, with cluster randomisation to method of NAT-C appointment delivery, and process evaluation. Adults with active cancer were invited to participate with or without carer. Practices cluster randomised (1:1) to Arm I: promotion and use of NAT-C with a NAT-C trained clinician or Arm II: clinician of choice irrespective of training status. Participants completed study questionnaires at: baseline, 1, 3 and 6 months. Patients booked a 20 minute needs-assessment appointment post-baseline. Patients, carers and GP practice staff views regarding the study sought through interviews/focus groups. Quantitative data were analysed descriptively. Qualitative data were analysed thematically, informed by Normalisation Process Theory. Progression to a definitive trial was assessed against feasibility outcomes, relating to: recruitment rate, uptake and delivery of the NAT-C, data collection and quality.
RESULTS
Five GP practices approached, four recruited and trained to use the NAT-C. Forty-seven participants and 17 carers recruited. At baseline, 34/47 (72%) participants reported at least one moderate-severe unmet need, confirming study rationale. 32/47 (68%) participants received a NAT-C-guided consultation, 19 of which on Arm I. Study attrition at one month (n = 44 (94%), n = 16 (94%)), three months (n = 38 (81%), n = 14 (82%)) and six months (n = 32 (68%), n = 10 (59%)). Fifteen patient interviews conducted across the whole study and one focus group at each GP practice. Participants supported a definitive study and found measures acceptable.
CONCLUSION
The feasibility trial indicated that recruitment rate, intervention uptake and data collection were appropriate, with refinements, for a definitive multi-centre cluster randomised controlled trial. Feasibility outcomes informed the design of a 2-armed cluster randomised controlled trial to test the effectiveness and cost-effectiveness of the NAT-C compared with usual care.

Identifiants

pubmed: 33507949
doi: 10.1371/journal.pone.0245647
pii: PONE-D-20-25507
pmc: PMC7842977
doi:

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0245647

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Références

Support Care Cancer. 2007 Oct;15(10):1125-44
pubmed: 17235503
Eur J Cancer. 2010 Sep;46(13):2381-8
pubmed: 20570138
J Pain Symptom Manage. 2012 Mar;43(3):569-81
pubmed: 22209224
Support Care Cancer. 2006 May;14(5):444-53
pubmed: 16402231
J Pain Symptom Manage. 2018 Oct;56(4):602-612
pubmed: 30009964
Patient Prefer Adherence. 2020 Jul 20;14:1205-1212
pubmed: 32764893
J Eval Clin Pract. 2004 May;10(2):307-12
pubmed: 15189396
BMJ. 2019 Apr 18;365:l1827
pubmed: 31000501
Cochrane Database Syst Rev. 2017 Jun 12;6:CD011129
pubmed: 28603881
BMC Palliat Care. 2018 Jul 23;17(1):96
pubmed: 30037346
BMJ Open. 2019 Aug 15;9(8):e029954
pubmed: 31420394
J Clin Oncol. 2011 Jul 20;29(21):2910-7
pubmed: 21690465
BMJ. 2017 Jul 4;357:j2925
pubmed: 28676557
Oncologist. 2016 Jul;21(7):895-901
pubmed: 27185614
BMJ Open. 2019 May 22;9(5):e020580
pubmed: 31122962
J Patient Rep Outcomes. 2018 Sep 15;2:42
pubmed: 30294712
Psychooncology. 2012 May;21(5):550-7
pubmed: 22517737
BMJ Open. 2016 Dec 9;6(12):e012576
pubmed: 27940628
BMJ. 2014 Mar 07;348:g1687
pubmed: 24609605
Fam Pract. 2007 Dec;24(6):601-3
pubmed: 17872907

Auteurs

Joseph Clark (J)

Wolfson Palliative Care Research Centre, University of Hull, Hull, United Kingdom.

Elvis Amoakwa (E)

Wolfson Palliative Care Research Centre, University of Hull, Hull, United Kingdom.

Alexandra Wright-Hughes (A)

Leeds Institute of Clinical Trials Research, University of Leeds, Leeds, United Kingdom.

John Blenkinsopp (J)

University of Northumbria, Newcastle upon Tyne, United Kingdom.

David C Currow (DC)

Wolfson Palliative Care Research Centre, University of Hull, Hull, United Kingdom.

David Meads (D)

Leeds Institute of Health Sciences, University of Leeds, Leeds, United Kingdom.

Amanda Farrin (A)

Leeds Institute of Clinical Trials Research, University of Leeds, Leeds, United Kingdom.

Victoria Allgar (V)

Hull York Medical School, University of York, York, United Kingdom.

Una Macleod (U)

Hull York Medical School, University of Hull, Hull, United Kingdom.

Miriam Johnson (M)

Wolfson Palliative Care Research Centre, University of Hull, Hull, United Kingdom.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH