The goal of this descriptive non-randomized feasibility study is to assess aspects of feasibility of the intervention arm in a planned full-scale randomized controlled trial testing the effectiveness of a self-management program for persons who have sustained a moderate to severe traumatic injury. All outcomes will be evaluated based on pre-defined success criteria. The main outcomes in the feasibility study are: * Consent rate of eligible patients * Drop-out rate * Attendance rate in the program sessions Secondary outcomes are the participants' acceptance, reception, and perceived usefulness. Other outcomes are fidelity and protocol adherence, as well as the feasibility of a telehealth version of the program and the data collection methods. The participants will receive a group-based self-management program consisting of eight weekly 2.5-hour sessions delivered by a multidisciplinary team. The self-management program is manualized and includes psychoeducation, training in self-management skills and strategies, setting goals, action planning, and sharing of experiences. The participants will also complete the pre- and post-intervention assessments.
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Consent rate of eligible
Timeframe: Will be evaluated after the intervention period, i.e. 2-3 months after inclusion
Drop-out rate
Timeframe: Will be evaluated after the intervention period, i.e. 2-3 months after inclusion
Attendance rate
Timeframe: Will be evaluated after the intervention period, i.e. 2-3 months after inclusion