Assessing decision regret in caregivers of deceased German people with cancer—A psychometric validation of the Decision Regret Scale for Caregivers. (31st July 2019)
- Record Type:
- Journal Article
- Title:
- Assessing decision regret in caregivers of deceased German people with cancer—A psychometric validation of the Decision Regret Scale for Caregivers. (31st July 2019)
- Main Title:
- Assessing decision regret in caregivers of deceased German people with cancer—A psychometric validation of the Decision Regret Scale for Caregivers
- Authors:
- Haun, Markus W.
Schakowski, Alexander
Preibsch, Ariane
Friederich, Hans‐Christoph
Hartmann, Mechthild - Abstract:
- Abstract: Background: Decisional regret during or after medical treatments is linked to significant distress. Regret affects not only patients but also caregivers having an active or passive role during decision making. The Decision Regret Scale (DRS) is a self‐report measure for regret in patients after treatment decisions. However, practical and psychometrically robust instruments assessing regret in caregivers are lacking. Objective: To develop and validate a caregiver version of the DRS (Decision Regret Scale for Caregivers [DRS‐C]). Design: Psychometric validation based on a web survey. Setting and participants: 361 caregivers of deceased German people/patients with cancer. Main variables studied: Besides structural validity and test‐retest reliability, we evaluated measurement invariance accounting for gender, age and closeness of relationship, and tested hypotheses on convergent/discriminant validity. Results: Forty‐five per cent of all caregivers demonstrated decision regret. Confirmatory factor analyses strongly supported the unidimensional structure of the DRS‐C and pointed to strict invariance. The DRS‐C demonstrated very good internal consistency ( α = 0.83, 95% CI [0.81, 0.86]) and test‐retest reliability (ICC [A, 1] = 0.73, 95% CI [0.59, 0.83]) along with sound convergent/discriminant validity. Concerning responsiveness, DRS‐C scores remained stable over a 12‐week period in 83.3% of all caregivers. Receiver operating characteristic analysis yielded a cut pointAbstract: Background: Decisional regret during or after medical treatments is linked to significant distress. Regret affects not only patients but also caregivers having an active or passive role during decision making. The Decision Regret Scale (DRS) is a self‐report measure for regret in patients after treatment decisions. However, practical and psychometrically robust instruments assessing regret in caregivers are lacking. Objective: To develop and validate a caregiver version of the DRS (Decision Regret Scale for Caregivers [DRS‐C]). Design: Psychometric validation based on a web survey. Setting and participants: 361 caregivers of deceased German people/patients with cancer. Main variables studied: Besides structural validity and test‐retest reliability, we evaluated measurement invariance accounting for gender, age and closeness of relationship, and tested hypotheses on convergent/discriminant validity. Results: Forty‐five per cent of all caregivers demonstrated decision regret. Confirmatory factor analyses strongly supported the unidimensional structure of the DRS‐C and pointed to strict invariance. The DRS‐C demonstrated very good internal consistency ( α = 0.83, 95% CI [0.81, 0.86]) and test‐retest reliability (ICC [A, 1] = 0.73, 95% CI [0.59, 0.83]) along with sound convergent/discriminant validity. Concerning responsiveness, DRS‐C scores remained stable over a 12‐week period in 83.3% of all caregivers. Receiver operating characteristic analysis yielded a cut point of 43 for the identification of significant decision regret (AUC = 0.62, 95% CI [0.56, 0.68]). Discussion and conclusions: The lack of a gold standard instrument prevented us from examining the criterion validity and determining a minimally important difference. Nevertheless, the DRS‐C provides valid and reliable information regarding caregiver regret following medical decisions. Above all, it captures a crucial aspect of the treatment experience in caregivers. … (more)
- Is Part Of:
- Health expectations. Volume 22:Number 5(2019)
- Journal:
- Health expectations
- Issue:
- Volume 22:Number 5(2019)
- Issue Display:
- Volume 22, Issue 5 (2019)
- Year:
- 2019
- Volume:
- 22
- Issue:
- 5
- Issue Sort Value:
- 2019-0022-0005-0000
- Page Start:
- 1089
- Page End:
- 1099
- Publication Date:
- 2019-07-31
- Subjects:
- aggressiveness of care -- cancer -- caregiver -- confirmatory factor analysis -- decision regret -- measurement invariance
Medical policy -- Periodicals
Public health -- Periodicals
Health planning -- Periodicals
362.105 - Journal URLs:
- http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=hex ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1369-7625 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/hex.12941 ↗
- Languages:
- English
- ISSNs:
- 1369-6513
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4275.015545
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 12006.xml