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Published in: BMC Medicine 1/2014

Open Access 01-12-2014 | Research article

Adaptation and validation of the Treatment Burden Questionnaire (TBQ) in English using an internet platform

Authors: Viet-Thi Tran, Magdalena Harrington, Victor M Montori, Caroline Barnes, Paul Wicks, Philippe Ravaud

Published in: BMC Medicine | Issue 1/2014

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Abstract

Background

Treatment burden refers to the workload imposed by healthcare on patients, and the effect this has on quality of life. The Treatment Burden Questionnaire (TBQ) aims to assess treatment burden in different condition and treatment contexts. Here, we aimed to evaluate the validity and reliability of an English version of the TBQ, a scale that was originally developed in French.

Methods

The TBQ was translated into English by a forward-backward translation method. Wording and possible missing items were assessed during a pretest involving 200 patients with chronic conditions. Measurement properties of the instrument were assessed online with a patient network, using the PatientsLikeMe website. Dimensional structure of the questionnaire was assessed by factor analysis. Construct validity was assessed by associating TBQ global score wıth clinical variables, adherence to medication assessed by Morisky’s Medication Adherence Scale (MMAS-8), quality of life (QOL) assessed by the PatientsLikeMe Quality of Life Scale (PLMQOL), and patients’ confidence in their knowledge of their conditions and treatments. Reliability was determined by a test–retest method.

Results

In total, 610 patients with chronic conditions, mainly from the USA, UK, Canada, Australia, or New Zealand, completed the TBQ between September and October 2013. The English TBQ showed a unidimensional structure with Cronbach α of 0.90. The TBQ global score was negatively correlated with the PLMQOL score (rs = −0.50; p < 0.0001). Low rather than moderate or high adherence to medication was associated with high TBQ score (mean [SD] TBQ score 61.8 [30.5] vs. 37.7 [27.5]; P < 0.0001). The treatment burden was higher for patients who had insufficient knowledge compared with those who had sufficient knowledge about their treatments (mean ± SD TBQ score 62.3 ± 31.3 vs. 47.8 ± 30.4; P < 0.0001) and conditions (63.0 ± 31.6 vs. 49.3 ± 30.7; P < 0.0001). The intraclass correlation coefficient for the retest (n = 282) was 0.77 (95% CI 0.70 to 0.82).

Conclusions

We found that the English TBQ is a reliable instrument in this population, and provide evidence supporting the construct validity for its use to assess treatment burden for patients with one or more chronic conditions in English-speaking countries.
Appendix
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Literature
1.
go back to reference May C, Montori VM, Mair FS: We need minimally disruptive medicine. BMJ. 2009, 339: b2803-10.1136/bmj.b2803.CrossRefPubMed May C, Montori VM, Mair FS: We need minimally disruptive medicine. BMJ. 2009, 339: b2803-10.1136/bmj.b2803.CrossRefPubMed
2.
go back to reference Eton DT, Ramalho de Oliveira D, Egginton JS, Ridgeway JL, Odell L, May CR, Montori VM: Building a measurement framework of burden of treatment in complex patients with chronic conditions: a qualitative study. Patient Relat Outcome Meas. 2012, 3: 39-49.CrossRefPubMedPubMedCentral Eton DT, Ramalho de Oliveira D, Egginton JS, Ridgeway JL, Odell L, May CR, Montori VM: Building a measurement framework of burden of treatment in complex patients with chronic conditions: a qualitative study. Patient Relat Outcome Meas. 2012, 3: 39-49.CrossRefPubMedPubMedCentral
3.
go back to reference Eton DT, Elraiyah TA, Yost KJ, Ridgeway JL, Johnson A, Egginton JS, Mullan RJ, Murad MH, Erwin PJ, Montori VM: A systematic review of patient-reported measures of burden of treatment in three chronic diseases. Patient Relat Outcome Meas. 2013, 4: 7-20.CrossRefPubMedPubMedCentral Eton DT, Elraiyah TA, Yost KJ, Ridgeway JL, Johnson A, Egginton JS, Mullan RJ, Murad MH, Erwin PJ, Montori VM: A systematic review of patient-reported measures of burden of treatment in three chronic diseases. Patient Relat Outcome Meas. 2013, 4: 7-20.CrossRefPubMedPubMedCentral
4.
go back to reference Jowsey T, Yen L, PM W: Time spent on health related activities associated with chronic illness: a scoping literature review. BMC Public Health. 2012, 12: 1044-10.1186/1471-2458-12-1044.CrossRefPubMedPubMedCentral Jowsey T, Yen L, PM W: Time spent on health related activities associated with chronic illness: a scoping literature review. BMC Public Health. 2012, 12: 1044-10.1186/1471-2458-12-1044.CrossRefPubMedPubMedCentral
5.
go back to reference Boyd CM, Darer J, Boult C, Fried LP, Boult L, Wu AW: Clinical practice guidelines and quality of care for older patients with multiple comorbid diseases: implications for pay for performance. JAMA. 2005, 294: 716-724. 10.1001/jama.294.6.716.CrossRefPubMed Boyd CM, Darer J, Boult C, Fried LP, Boult L, Wu AW: Clinical practice guidelines and quality of care for older patients with multiple comorbid diseases: implications for pay for performance. JAMA. 2005, 294: 716-724. 10.1001/jama.294.6.716.CrossRefPubMed
6.
go back to reference Guthrie B, Payne K, Alderson P, McMurdo ME, Mercer SW: Adapting clinical guidelines to take account of multimorbidity. BMJ. 2012, 345: e6341-10.1136/bmj.e6341.CrossRefPubMed Guthrie B, Payne K, Alderson P, McMurdo ME, Mercer SW: Adapting clinical guidelines to take account of multimorbidity. BMJ. 2012, 345: e6341-10.1136/bmj.e6341.CrossRefPubMed
7.
go back to reference Montori VM, Brito JP, Murad MH: The optimal practice of evidence-based medicine: incorporating patient preferences in practice guidelines. JAMA. 2013, 310: 2503-2504. 10.1001/jama.2013.281422.CrossRefPubMed Montori VM, Brito JP, Murad MH: The optimal practice of evidence-based medicine: incorporating patient preferences in practice guidelines. JAMA. 2013, 310: 2503-2504. 10.1001/jama.2013.281422.CrossRefPubMed
8.
go back to reference Bohlen K, Scoville E, Shippee ND, May CR, Montori VM: Overwhelmed patients: a videographic analysis of how patients with type 2 diabetes and clinicians articulate and address treatment burden during clinical encounters. Diabetes Care. 2012, 35: 47-49. 10.2337/dc11-1082.CrossRefPubMed Bohlen K, Scoville E, Shippee ND, May CR, Montori VM: Overwhelmed patients: a videographic analysis of how patients with type 2 diabetes and clinicians articulate and address treatment burden during clinical encounters. Diabetes Care. 2012, 35: 47-49. 10.2337/dc11-1082.CrossRefPubMed
9.
go back to reference Tran VT, Montori VM, Eton DT, Baruch D, Falissard B, Ravaud P: Development and description of measurement properties of an instrument to assess Treatment Burden among patients with multiple chronic conditions. BMC Med. 2012, 10: 68-10.1186/1741-7015-10-68.CrossRefPubMedPubMedCentral Tran VT, Montori VM, Eton DT, Baruch D, Falissard B, Ravaud P: Development and description of measurement properties of an instrument to assess Treatment Burden among patients with multiple chronic conditions. BMC Med. 2012, 10: 68-10.1186/1741-7015-10-68.CrossRefPubMedPubMedCentral
10.
go back to reference Eton DT, Oliveira DR, Egginton J, Mair FS, May C, Montori VM: Understanding the burden of treatment in patients with multiple chronic conditions: Evidence from exploratory interviews. Qual Life Res. 2010, 19: ab-1673CrossRef Eton DT, Oliveira DR, Egginton J, Mair FS, May C, Montori VM: Understanding the burden of treatment in patients with multiple chronic conditions: Evidence from exploratory interviews. Qual Life Res. 2010, 19: ab-1673CrossRef
11.
12.
go back to reference Acquadro C, Conway K, Hareendran A, Aaronson N: Literature review of methods to translate health-related quality of life questionnaires for use in multinational clinical trials. Value Health. 2008, 11: 509-521. 10.1111/j.1524-4733.2007.00292.x.CrossRefPubMed Acquadro C, Conway K, Hareendran A, Aaronson N: Literature review of methods to translate health-related quality of life questionnaires for use in multinational clinical trials. Value Health. 2008, 11: 509-521. 10.1111/j.1524-4733.2007.00292.x.CrossRefPubMed
13.
go back to reference Beaton DE, Bombardier C, Guillemin F, Ferraz MB: Guidelines for the process of cross-cultural adaptation of self-report measures. Spine (Phila Pa 1976). 2000, 25: 3186-3191. 10.1097/00007632-200012150-00014.CrossRef Beaton DE, Bombardier C, Guillemin F, Ferraz MB: Guidelines for the process of cross-cultural adaptation of self-report measures. Spine (Phila Pa 1976). 2000, 25: 3186-3191. 10.1097/00007632-200012150-00014.CrossRef
14.
go back to reference Wild D, Grove A, Martin M, Eremenco S, McElroy S, Verjee-Lorenz A, Erikson P: Principles of good practice for the translation and cultural adaptation process for patient-reported outcomes (PRO) measures: report of the ISPOR Task Force for Translation and Cultural Adaptation. Value Health. 2005, 8: 94-104. 10.1111/j.1524-4733.2005.04054.x.CrossRefPubMed Wild D, Grove A, Martin M, Eremenco S, McElroy S, Verjee-Lorenz A, Erikson P: Principles of good practice for the translation and cultural adaptation process for patient-reported outcomes (PRO) measures: report of the ISPOR Task Force for Translation and Cultural Adaptation. Value Health. 2005, 8: 94-104. 10.1111/j.1524-4733.2005.04054.x.CrossRefPubMed
15.
go back to reference Gallacher K, May CR, Montori VM, Mair FS: Understanding patients’ experiences of treatment burden in chronic heart failure using normalization process theory. Ann Fam Med. 2011, 9: 235-243. 10.1370/afm.1249.CrossRefPubMedPubMedCentral Gallacher K, May CR, Montori VM, Mair FS: Understanding patients’ experiences of treatment burden in chronic heart failure using normalization process theory. Ann Fam Med. 2011, 9: 235-243. 10.1370/afm.1249.CrossRefPubMedPubMedCentral
16.
go back to reference Gallacher K, Morrison D, Jani B, Macdonald S, May CR, Montori VM, Erwin PJ, Batty GD, Eton DT, Langhorne P, Mair FS: Uncovering treatment burden as a key concept for stroke care: a systematic review of qualitative research. PLoS Med. 2013, 10: e1001473-10.1371/journal.pmed.1001473.CrossRefPubMedPubMedCentral Gallacher K, Morrison D, Jani B, Macdonald S, May CR, Montori VM, Erwin PJ, Batty GD, Eton DT, Langhorne P, Mair FS: Uncovering treatment burden as a key concept for stroke care: a systematic review of qualitative research. PLoS Med. 2013, 10: e1001473-10.1371/journal.pmed.1001473.CrossRefPubMedPubMedCentral
17.
go back to reference Sav A, Kendall E, McMillan SS, Kelly F, Whitty JA, King MA, Wheeler AJ: ‘You say treatment, I say hard work’: treatment burden among people with chronic illness and their carers in Australia. Health Soc Care Community. 2013, 21: 665-674.PubMed Sav A, Kendall E, McMillan SS, Kelly F, Whitty JA, King MA, Wheeler AJ: ‘You say treatment, I say hard work’: treatment burden among people with chronic illness and their carers in Australia. Health Soc Care Community. 2013, 21: 665-674.PubMed
19.
go back to reference Wicks P, Heywood B, Heywood J: Online platform to accelerate patient involvement in open instrument development. Qual Life Res. 2013, 22: 55. Wicks P, Heywood B, Heywood J: Online platform to accelerate patient involvement in open instrument development. Qual Life Res. 2013, 22: 55.
21.
go back to reference Cronbach L: Coefficient alpha and the internal structure of tests. Psychometrika. 1951, 16: 297-334. 10.1007/BF02310555.CrossRef Cronbach L: Coefficient alpha and the internal structure of tests. Psychometrika. 1951, 16: 297-334. 10.1007/BF02310555.CrossRef
22.
go back to reference Nunnaly J, Bernstein I: Psychometric theory. 1994, New York: McGraw-Hill, 3 Nunnaly J, Bernstein I: Psychometric theory. 1994, New York: McGraw-Hill, 3
23.
go back to reference Slawsky K, Massagli M, Wicks P: PRM30 a comparison of the PatientsLikeMe Quality of Life Questionnaire (PLMQOL) with the RAND SF-36. Value Health. 2011, 14: A426.CrossRef Slawsky K, Massagli M, Wicks P: PRM30 a comparison of the PatientsLikeMe Quality of Life Questionnaire (PLMQOL) with the RAND SF-36. Value Health. 2011, 14: A426.CrossRef
24.
go back to reference Morisky DE, Ang A, Krousel-Wood M, Ward HJ: Predictive validity of a medication adherence measure in an outpatient setting. J ClinHypertens (Greenwich). 2008, 10: 348-354. 10.1111/j.1751-7176.2008.07572.x.CrossRef Morisky DE, Ang A, Krousel-Wood M, Ward HJ: Predictive validity of a medication adherence measure in an outpatient setting. J ClinHypertens (Greenwich). 2008, 10: 348-354. 10.1111/j.1751-7176.2008.07572.x.CrossRef
25.
go back to reference Morisky DE, Green LW, Levine DM: Concurrent and predictive validity of a self-reported measure of medication adherence. Med Care. 1986, 24: 67-74. 10.1097/00005650-198601000-00007.CrossRefPubMed Morisky DE, Green LW, Levine DM: Concurrent and predictive validity of a self-reported measure of medication adherence. Med Care. 1986, 24: 67-74. 10.1097/00005650-198601000-00007.CrossRefPubMed
26.
go back to reference Diederichs C, Berger K, Bartels DB: The measurement of multiple chronic diseases–a systematic review on existing multimorbidity indices. J Gerontol A BiolSci Med Sci. 2011, 66: 301-311.CrossRef Diederichs C, Berger K, Bartels DB: The measurement of multiple chronic diseases–a systematic review on existing multimorbidity indices. J Gerontol A BiolSci Med Sci. 2011, 66: 301-311.CrossRef
27.
go back to reference Juniper E, Guyatt G, Jaeschke R: How to develop and validate a new health-related quality of life instrument. Quality of life and pharmacoeconomics in clinical trials. Edited by: Spilker B. 1996, Philadelphia - New York: Lippincott - Raven, 49-56. Juniper E, Guyatt G, Jaeschke R: How to develop and validate a new health-related quality of life instrument. Quality of life and pharmacoeconomics in clinical trials. Edited by: Spilker B. 1996, Philadelphia - New York: Lippincott - Raven, 49-56.
28.
go back to reference Shrout PE, Fleiss JL: Intraclass correlations: uses in assessing rater reliability. Psychol Bull. 1979, 86: 420-428.CrossRefPubMed Shrout PE, Fleiss JL: Intraclass correlations: uses in assessing rater reliability. Psychol Bull. 1979, 86: 420-428.CrossRefPubMed
29.
go back to reference Streiner D, Norman G: Health Measurement Scales: a practical guide to their development and use, Fourth Edition edn. 2008, Oxford: Oxford University PressCrossRef Streiner D, Norman G: Health Measurement Scales: a practical guide to their development and use, Fourth Edition edn. 2008, Oxford: Oxford University PressCrossRef
30.
go back to reference Bland JM, Altman DG: Measuring agreement in method comparison studies. Stat Methods Med Res. 1999, 8: 135-160. 10.1191/096228099673819272.CrossRefPubMed Bland JM, Altman DG: Measuring agreement in method comparison studies. Stat Methods Med Res. 1999, 8: 135-160. 10.1191/096228099673819272.CrossRefPubMed
32.
go back to reference Ubel PA, Abernethy AP, Zafar SY: Full disclosure–out-of-pocket costs as side effects. N Engl J Med. 2013, 369: 1484-1486. 10.1056/NEJMp1306826.CrossRefPubMed Ubel PA, Abernethy AP, Zafar SY: Full disclosure–out-of-pocket costs as side effects. N Engl J Med. 2013, 369: 1484-1486. 10.1056/NEJMp1306826.CrossRefPubMed
33.
go back to reference Ekman A, Litton JE: New times, new needs; e-epidemiology. Eur J Epidemiol. 2007, 22: 285-292. 10.1007/s10654-007-9119-0.CrossRefPubMed Ekman A, Litton JE: New times, new needs; e-epidemiology. Eur J Epidemiol. 2007, 22: 285-292. 10.1007/s10654-007-9119-0.CrossRefPubMed
34.
go back to reference Bove R, Secor E, Healy BC, Musallam A, Vaughan T, Glanz BI, Greeke E, Weiner HL, Chitnis T, Wicks P, De Jager PL: Evaluation of an online platform for multiple sclerosis research: patient description, validation of severity scale, and exploration of BMI effects on disease course. PLoS One. 2013, 8: e59707-10.1371/journal.pone.0059707.CrossRefPubMedPubMedCentral Bove R, Secor E, Healy BC, Musallam A, Vaughan T, Glanz BI, Greeke E, Weiner HL, Chitnis T, Wicks P, De Jager PL: Evaluation of an online platform for multiple sclerosis research: patient description, validation of severity scale, and exploration of BMI effects on disease course. PLoS One. 2013, 8: e59707-10.1371/journal.pone.0059707.CrossRefPubMedPubMedCentral
35.
go back to reference Wicks P, Sulham KA, Gnanasakthy A: Quality of life in organ transplant recipients participating in an online transplant community. Patient. 2014, 7: 73-84. 10.1007/s40271-013-0033-0.CrossRefPubMed Wicks P, Sulham KA, Gnanasakthy A: Quality of life in organ transplant recipients participating in an online transplant community. Patient. 2014, 7: 73-84. 10.1007/s40271-013-0033-0.CrossRefPubMed
36.
go back to reference De la Loge C, Keininger D, Isojärvi J, Massagli MP, Wicks P: Characteristics of users of the epilepsy community of PatientsLikeMe.com and comparison with a representative claims database. 63rd Annual Meeting of the American Academy of Neurology. 2011, Honolulu, USA De la Loge C, Keininger D, Isojärvi J, Massagli MP, Wicks P: Characteristics of users of the epilepsy community of PatientsLikeMe.com and comparison with a representative claims database. 63rd Annual Meeting of the American Academy of Neurology. 2011, Honolulu, USA
37.
go back to reference Bowden A, Fox-Rushby JA: A systematic and critical review of the process of translation and adaptation of generic health-related quality of life measures in Africa, Asia, Eastern Europe, the Middle East, South America. Soc Sci Med. 2003, 57: 1289-1306. 10.1016/S0277-9536(02)00503-8.CrossRefPubMed Bowden A, Fox-Rushby JA: A systematic and critical review of the process of translation and adaptation of generic health-related quality of life measures in Africa, Asia, Eastern Europe, the Middle East, South America. Soc Sci Med. 2003, 57: 1289-1306. 10.1016/S0277-9536(02)00503-8.CrossRefPubMed
Metadata
Title
Adaptation and validation of the Treatment Burden Questionnaire (TBQ) in English using an internet platform
Authors
Viet-Thi Tran
Magdalena Harrington
Victor M Montori
Caroline Barnes
Paul Wicks
Philippe Ravaud
Publication date
01-12-2014
Publisher
BioMed Central
Published in
BMC Medicine / Issue 1/2014
Electronic ISSN: 1741-7015
DOI
https://doi.org/10.1186/1741-7015-12-109

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