Funding for this research was provided by:
ZonMW, Netherlands Organisation for Health Care Research and Development (520001001)
Received: 7 June 2018
Accepted: 23 November 2018
First Online: 12 December 2018
Ethics approval and consent to participate
: Individuals who were referred to the IMR-programme were informed about the trial by their case manager. The researcher contacted those who expressed an interest individually and explained the trial and research activities. If they were still interested and eligible, the written consent to participate was signed. No incentives were provided. The ethical approval for conducting the e-IMR trial was provided by the Committee on Research Involving Human Subjects, Arnhem-Nijmegen (NL49693.091.14).
: Not applicable.
: The authors declare that they have no competing interests.
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