Resistance Training and Nutritional Supplementation in Older Adults with Sarcopenia after Acute Disease: A Feasibility Study

Author:

Meza-Valderrama Delky1234ORCID,Sánchez-Rodríguez Dolores15ORCID,Peña Yulibeth Curbelo16,Ramírez-Fuentes Cindry16,Muñoz-Redondo Elena16ORCID,Morgado-Pérez Andrea16,Ortíz-Agurto Norma27,Finis-Gallardo Paola2,Marco Ester168ORCID

Affiliation:

1. Rehabilitation Research Group, Hospital del Mar Medical Research Institute, 08024 Barcelona, Catalonia, Spain

2. Physical Medicine and Rehabilitation Department, National Institute of Physical Medicine and Rehabilitation, Panama City 0819, Panama

3. Physical Medicine and Rehabilitation Center, Ciudad de la Salud, Caja de Seguro Social, Panama City 0819, Panama

4. Sistema Nacional de Investigación (SENACYT), Panama City 0824, Panama

5. Geriatrics Department, Brugmann University Hospital, Université Libre de Bruxelles, 1050 Brussels, Belgium

6. Physical Medicine and Rehabilitation Department, Parc de Salut Mar (Hospital del Mar, Hospital de l’Esperança), 08024 Barcelona, Catalonia, Spain

7. Faculty of Health and Life Sciences, Metropolitan University of Education, Science and Technology (UMECIT), Panama City 0819, Panama

8. Faculty of Health and Life Sciences, Universitat Pompeu Fabra, Dr. Aiguader Building (Mar Campus), Dr. Aiguader 80, 08003 Barcelona, Catalonia, Spain

Abstract

Resistance exercise and protein supplementation are recognized as effective treatment strategies for age-related sarcopenia; however, there are limited data on their feasibility, tolerability, and safety. The primary outcome of this study was feasibility, evaluated through the 15-item TELOS (Technological, Economics, Legal, Operational, and Scheduling) feasibility components and by recruitment, retention, and consent rates. Tolerability was measured by examining permanent treatment discontinuation, treatment interruption, exercise dose modification, early termination, rescheduling of missed sessions, losses to follow-up, attendance, and nutritional compliance. Safety was evaluated using the parameters provided by the European Medicines Agency, adapted for exercise interventions. Thirty-two subjects were recruited (average age 81.6 [SD 9.3] years). The TELOS components were assessed before the intervention; out of 15 questions relevant for successful implementation, 4 operational needs answers required specific actions to prevent potential barriers. The recruitment rate was 74%. Eleven patients (34.4%) had permanent treatment interruption (retention rate = 65.6%). Patients attended a mean of 23 (SD 12.0) exercise sessions, with a mean of 56 (SD 32.6) nutritional compliances. A total of 21 patients (65.6%) experienced adverse events unrelated to the intervention, while 7 patients (21.9%) presented adverse reactions to strength exercise. The main barriers to feasibility were operational components and recruitment challenges. Although the intervention was generally safe, the high rate of probable adverse effects, unrelated to the intervention but associated with the individual’s baseline health condition, may affect adherence to treatment programs of this kind.

Funder

Nutricia Research Foundation

Publisher

MDPI AG

Reference65 articles.

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