Abstract
Background
Telehealth is one of the ways in which the UK health service is seeking to improve the care of people living with a long-term condition. One of the aims of its “3 million lives” program is to achieve more effective self care. A lot of the research into telehealth has focused on cost effectiveness, effective working practices, and barriers to adoption. Patient experience is frequently discussed in terms of the reassurance experienced from the support offered through telehealth systems.
Objective
This study reports the qualitative findings of an evaluation of a local telehealth program introduced by the Dorset Clinical Commissioning Group for patients with chronic obstructive pulmonary disease or chronic heart failure.
Methods
Twenty-nine patients participated in telephone interviews, held at the start of their telehealth experience and after they had been using the system for 3 months. Interviewees included people who had graduated from the telehealth system or had asked to come off it. Healthcare professionals, mainly nurses, involved in the management of patients using the system were also interviewed.
Results
The evaluation found that patients were using the telehealth equipment, often beyond the parameters of the formal telehealth scheme, to develop effective self-management techniques.
Conclusion
These results have implications for policy makers, as removing the equipment when patients graduate as being self managing may mean removing the very tools that make that self management possible.
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Acknowledgments
This service evaluation was carried out on behalf of the Dorset Clinical Commissioning Group, who funded the project.
Carol Bond was responsible for the design and management of the evaluation and for drafting the paper, and is the guarantor for the study.
Louise Worswick was responsible for conducting interviews and data analysis, and contributed to the drafting of the paper.
Conflicts of interest
There are no conflicts of interest for either author.
The funder had no direct involvement in carrying out the evaluation or in the preparation of the paper.
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Appendix
Appendix
1.1 Patient Interviews
1.1.1 Semistructured Interview Schedule
(Confirm consent for recording.)
(Check length of time on telehealth.)
“Tell me about how you’ve been getting on with using telehealth.” (Explore successes and problems.)
“How does it fit into your daily routine?” (Comfortable fit or disruptive?)
“What happens to your results?” (Explore feedback and communications.)
“How has your care changed since going onto telehealth?” (Explore satisfaction with changes.)
“When you were discussing going onto telehealth, were the reasons discussed with you?” (Explore how was goal setting was done.)
“Can you sum up how you feel about telehealth so far?”
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Bond, C.S., Worswick, L. Self Management and Telehealth: Lessons Learnt from the Evaluation of a Dorset Telehealth Program. Patient 8, 311–316 (2015). https://doi.org/10.1007/s40271-014-0091-y
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DOI: https://doi.org/10.1007/s40271-014-0091-y