Literature DB >> 9780528

The role of pilot studies in the economic evaluation of health technologies.

M Drummond1, D Coyle.   

Abstract

An increasing number of economic evaluations are being conducted alongside clinical trials. While this practice offers the prospect of collecting comprehensive and accurate cost data, it requires considerable time and effort. In the case of clinical data, key analytic decisions such as which data to collect and sample size are often made with reference to smaller (pilot) trials. However, this approach is not normally followed in the case of economic evaluation. This study was based on a recently completed health technology assessment comparing conventional radiotherapy with continuous hyperfractionated accelerated radiotherapy (CHART) for patients with head and neck cancer or carcinoma of the bronchus. In the full health technology assessment, cost data were available for 526 head and neck patients (314 CHART and 212 conventional therapy) and 286 bronchus patients (175 CHART and 109 conventional therapy). In order to simulate a pilot study, data were extracted for the patients recruited to both trials in the first 3 months. These were then compared with the full data set in order to assess whether such a pilot study would have given useful guidance on: a) the usefulness of undertaking a full study; b) the sample size required; and c) the important resource items for which comprehensive data collection would be required. Pilot studies can be helpful in determining the likely advantages of undertaking full economic evaluations and in identifying important resource items. Therefore, it is important that clinical researchers and research funding bodies create the necessary time window to enable such studies to take place. However, formal sample size calculations are more difficult to perform on limited data, since they also require knowledge of the unit cost (or prices) to be attached to the resource items and the correlation between costs and clinical effects.

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Year:  1998        PMID: 9780528     DOI: 10.1017/s0266462300011399

Source DB:  PubMed          Journal:  Int J Technol Assess Health Care        ISSN: 0266-4623            Impact factor:   2.188


  4 in total

1.  Describing the characteristics, treatment pathways, outcomes, and costs of people with persistent noncancer pain managed by community pain clinics and generating an indicative estimate of cost-effectiveness: feasibility study protocol.

Authors:  Shiekha AlAujan; Saja AlMazrou; Roger D Knaggs; Rachel A Elliott
Journal:  J Multidiscip Healthc       Date:  2016-05-18

2.  Effectiveness of a tailored rehabilitation versus standard strengthening programme for patients with shoulder pain: a protocol for a feasibility randomised controlled trial (the Otago MASTER trial).

Authors:  Daniel C Ribeiro; Zohreh Jafarian Tangrood; Gisela Sole; J Haxby Abbott
Journal:  BMJ Open       Date:  2019-07-30       Impact factor: 2.692

3.  Michigan Model for HealthTM Learning to Enhance and Adapt for Prevention (Mi-LEAP): protocol of a pilot randomized trial comparing Enhanced Replicating Effective Programs versus standard implementation to deliver an evidence-based drug use prevention curriculum.

Authors:  Andria B Eisman; Lawrence A Palinkas; Christine Koffkey; Todd I Herrenkohl; Umaima Abbasi; Judy Fridline; Leslie Lundahl; Amy M Kilbourne
Journal:  Pilot Feasibility Stud       Date:  2022-09-10

4.  Palliative long-term abdominal drains versus repeated drainage in individuals with untreatable ascites due to advanced cirrhosis: study protocol for a feasibility randomised controlled trial.

Authors:  Lucia Macken; Louise Mason; Catherine Evans; Heather Gage; Jake Jordan; Mark Austin; Nick Parnell; Max Cooper; Shani Steer; Justine Boles; Stephen Bremner; Debbie Lambert; David Crook; Gemma Earl; Jean Timeyin; Sumita Verma
Journal:  Trials       Date:  2018-07-27       Impact factor: 2.279

  4 in total

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