Feasibility of a comprehensive supervised exercise program during and after treatment of head and neck cancer: a mixed-methods study

被引:0
作者
Van Aperen, Kaat [1 ,2 ]
De Groef, An [2 ,3 ]
Troosters, Thierry [2 ,4 ]
Elshout, Pascalle [5 ]
Nuyts, Sandra [1 ,6 ]
机构
[1] Univ Leuven, Dept Oncol, Lab Expt Radiotherapy, Louvain, Belgium
[2] Univ Leuven, Dept Rehabil Sci & Physiotherapy, Louvain, Belgium
[3] Univ Antwerp, Dept Rehabil Sci & Physiotherapy, MOVANT Res Grp, Antwerp, Belgium
[4] Univ Hosp Leuven, Resp Rehabil & Resp Div, Louvain, Belgium
[5] Berekuyl Acad, Hierden, Netherlands
[6] Univ Hosp Leuven, Leuven Canc Inst, Dept Radiat Oncol, Louvain, Belgium
关键词
Feasibility; Exercise program; Head and neck cancer; Focus groups; QUALITY-OF-LIFE; PHYSICAL-ACTIVITY; SEDENTARY BEHAVIOR; SURVIVORS; ADHERENCE; PREDICTORS; PREVENTION; PATIENT; PILOT; TRIAL;
D O I
10.1007/s00520-024-09112-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PurposeThis study evaluates the feasibility of a comprehensive supervised exercise program (CSEP) for head and neck cancer (HNC) patients during and after (chemo)radiotherapy, integrating quantitative and qualitative data to identify participation barriers and facilitators.MethodsTo investigate the feasibility of the CSEP, a mixed-method study was performed. For the quantitative part, first, adherence to and safety of the CSEP were considered as quantitative feasibility outcome measures. Second, two questionnaires evaluated acceptability, adherence, feasibility, therapeutic support, and overall evaluation at 12 weeks and 6 months after the start of the radiotherapy. Additionally, focus groups were held to discuss acceptability, adherence, expectations, feasibility, therapeutic support, and overall evaluation. The quantitative and qualitative data were integrated and discussed via a joint display table.ResultsQuantitative data were available from 32 participants. Three focus groups with in total 11 participants were organized. Overall adherence to the CSEP was 72%, and no serious adverse events were reported, confirming the program's safety. Adherence and feasibility posed challenges; hospital sessions had higher adherence due to better motivation and guidance, whereas home sessions faced issues like lack of motivation and time constraints. Participants highlighted the program's individualization as a significant strength.ConclusionThe CSEP was positively received, deemed safe, and feasible during and after HNC treatment, with participants recommending it to other HNC patients.Trial registrationTrial Registration: ClinicalTrials.gov Identifier: NCT05256238 (Registered on February 25, 2022).
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页数:27
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