Background: Pediatric palliative care programs aim to improve the quality of life of children with severe life-threatening illnesses, and that of their families. Although rehabilitation and physical therapy provides a valuable tool for the control of symptoms, it has been poorly researched to date. Since the family represents such a fundamental support in these cases, it is important to deepen our understanding regarding the value of implementing rehabilitation programs from the parents' perspective.

Aim: The aim of this paper was to explore parents' experiences regarding the implementation of a physical rehabilitation program in pediatric palliative care.

Design: A qualitative methodology was chosen.

Setting: The unit of pediatric palliative care at the Hospital Niño Jesús (Madrid, Spain).

Population: The inclusion criteria were: 1) parents of children, irrespective of their diagnosis; 2) integrated within the program of palliative care at the time of study; 3) aged between 0-18 years; 4) must be receiving Home-Based Rehabilitation Program by the Pediatric Palliative Care team. Fourteen parents were included.

Methods: Purposeful sampling method was implemented. Data collection consisted of unstructured and semi-structured interviews. A thematic analysis was performed to interpret transcripts. Guidelines for conducting qualitative studies established by the Consolidated Criteria for Reporting Qualitative Research were followed.

Results: Three main themes were identified: 1) the meaning of physical rehabilitation to parents; 2) physical rehabilitation as an opportunity for patients to stay in their home environment; and 3) home-based physical rehabilitation as part of the families' social environment.

Conclusions: The main needs of a home physical rehabilitation program are to decrease pain and suffering, together with improving family education and training.

Clinical Rehabilitation Impact: The experience of rehabilitation programs at home is essential in order to improve both the quality of life and the quality of care of affected children and parents.

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http://dx.doi.org/10.23736/S1973-9087.19.05474-1DOI Listing

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