ABSTRACT
Background
Traumatic brain injury significantly impacts survivors and their families. Rehabilitation following traumatic brain injury is often complex due to the physical, psychological, and socio-economic problems survivors face. Life goals are considered a motivational factor in rehabilitation.
Objective
The aim was to explore expectations, problems, and strategies for goal setting in survivors of traumatic brain injury and their family caregivers for one-year during rehabilitation.
Methods
A longitudinal qualitative study using dyadic interviews with survivors and family caregivers was carried out at three time points during the first year following traumatic brain injury. Data was analyzed according to Braun and Clarke’s thematic analysis.
Results
Eight survivors of traumatic brain injury and their family caregivers completed 24 interviews. Three themes and one sub-theme were identified: 1) life goals as a driving force (subtheme: dyadic discrepancies and conflicts); 2) conflicts between specific, measurable, achievable, realistic, and timed (SMART) goals and life goals; and 3) changing perceptions of the impact of impairments.
Conclusions
Life goals are important motivation in the rehabilitation process. Health care professionals must integrate life goals and rehabilitation goals (i.e. SMART goals) to decrease barriers and survivor ambivalence about rehabilitation. Involving both survivors and family caregivers in goal setting increases rehabilitation success.
Acknowledgments
We sincerely thank all participants who gave of their time and shared their personal stories. The authors also indebted to the International Workshop for Academic Writing that took place in September 2019 led by Niels Sandholm, Bjørg Christiansen, and Helle Mather at the Inter-University Center, Dubrovnik, Croatia.
Disclosure statement
No potential conflict of interest was reported by the author(s).
Consent
All participants gave informed consent to participate in the research.
Ethical considerations
The Danish Data Protection Agency (file no. 2012-41-1420) approved the study, which complies the Helsinki Declaration in terms of anonymity, informed consent, and data security (32). Participants were informed that participation was voluntary, that data would be anonymized, and that withdrawal was possible at any time, with no impact on their treatment or care. Neither interviewer worked at the hospital or municipalities involved and were not involved in patient care.