Sample size calculations were performed using the G*Power 3.1.9.4 software (Kiel University, Kiel, Germany), selecting the statistical test to compare the difference between two independent means (two groups). Thus, accepting an alpha risk of 0.05 and a beta risk of 0.2 in a bilateral contrast and assuming a moderate effect size of 0.5, a total of 160 participants (80 subjects in the experimental group and 80 in the control group) were sufficient to reach a minimum potency of 90%.
2.4. Randomisation and BlindingParticipants will be randomly assigned to the experimental (active retirement programme) or control groups. To assign participants to each group (1:1), Research Randomizer software (version 4.0, Geof-frey C. Urbaniak and Scott Plous, Middletown, CT, USA; http://www.randomizer.org, accessed 12 June 2022) will be used to create a randomisation sequence. A member of the research team, who will not participate in the intervention, will carry out this process. Group assignment will be hidden in a password-protected computer file. Participants will know their group assignment, but outcome assessors and data analysts will not know the participants’ group assignment. 2.5. ParticipantsParticipants must meet the following inclusion criteria: (1) be retired; (2) be aged between 55 and 80; (3) show their agreement to participate in the study by providing a signed consent form; (4) be individuals without dentures (except dental prosthesis); and (4) not have undergone surgery for less than six months. Exclusion criteria will be individuals with (1) musculoskeletal diseases; (2) locomotion issues; (3) psychiatric disorders; (4) neurological disorders; and (5) cardiovascular diseases.
2.6. InterventionExperimental group: This sensorimotor training programme will be carried out for six months, twice per week. As shown in Figure 1, as the programme progresses the load will be progressively increased.Sessions will be divided into three intensity levels: easy (no external load during the first eight weeks), intermediate (application of external load: elastic bands, shin guards, and free weights, from the 9th week to the 16th week) and advanced (increase in external load for the previous level, from the 17th week to the 24th week). Each month, a different type of session will be developed (Figure 2). Each session will last 45 min and will be divided into three phases: an initial one, consisting of a 5 min walk followed by a joint warm-up (10 min); a fundamental phase (25 min), working on exercises circuits consisting of four cycles, with eight exercises each (50 s on and 15 s off); and a return to calm with muscle stretching (10 min). Additionally, at the end of every session, the intensity will be assessed using the Borg Rating of Perceived Exertion Scale, and the level of satisfaction of the participants will be assessed employing the Physical Activity Enjoyment Scale (PACES) [24].Control group: Individuals will continue with their normal daily routine, only participating in the assessments. They will be offered to perform the exercise programme when the study ends.
Moreover, to guarantee participants’ safety, different strategies will be applied:
-Anamnesis of all participants;
-Hygiene of the material to be used during the sessions;
-Breaks between exercises;
-More than one researcher assisting with the sessions;
-Application of the effort scale.
2.7. MeasuresA variety of tools will be used. All measures will be undertaken at baseline, at the end of the intervention, and one year after the end of the intervention (follow-up). Before the first measurement, all participants will go through a familiarisation phase to familiarise themselves with the different instruments and assessments included in this project.
a. Anthropometrics and body composition. Bodyweight and height will be assessed. Before the measurements, participants will be asked to remove their shoes, socks, and heavy clothing (coats, sweaters, coats, etc.). They will also be asked to empty their pockets and remove belts and other accessories (bands, pendants, etc.). Height will be measured using a stadiometer (Seca 22, Hamburg, Germany). This instrument must be placed on a vertical surface with the measuring scale perpendicular to the ground. Participants will be positioned in a standing position, with their shoulders balanced, and their arms relaxed along their body. Height will be taken in cm and rounded to the nearest mm. Body weight will be measured using a scale. Body weight will be recorded in kg. and the body mass index (BMI) will be determined using the formula: weight × height2.
b. Physical fitness. Participants will wear tracksuit bottoms and will be asked to remove accessories and any objects in their pockets. The following measures will be carried out (Figure 3): (I) agility and execution speed will be assessed through the Timed Up and Go (TUG) test, which consists of getting up from a chair, walking in a straight line three meters away, and walking back and sitting down again [25]; (II and III) postural control will be tested through a force platform (Ber-tec4060-Columbus; USA). The assessment will consist of measuring the oscillations in a static bipedal position, with eyes open (two minutes) and with eyes closed (two minutes) [26]; (IV) gait will be assessed using the mobile application “Phyphox” on the surface of the skin, at the inner edge of the tibia, to quantify the number of steps and time. Participants will be asked to walk a pre-established route, without slopes or obstacles, for 10 min, at their natural cadence and, later, walk the same route at a pace determined by complex stimuli (auditory metronome—loudspeakers, which allow for hearing beats that correspond to steps) [27]; (V) muscular endurance will be assessed by rising up from the chair or bending and straightening for 30 s, during which the strength of the lower limbs involving the vastus medialis obliquus (VMO) and the vastus lateralis (VL) will also be calculated [28]; (VI) upper limb strength will be determined by the number of times that a weight can be lifted by performing a flexion–extension of the arms for 30 s [28]; (VII and VIII) flexibility will be evaluated by two tests: “the sit and reach” for lower limb flexibility, where participants, from a seated position with one leg extended, will slowly bend down, sliding their hands down the extended leg until they touch (or pass) their toes [28]; and “the behind the back reach” test for upper limbs, assessing the shoulder’s full range of motion, which will consist of measuring with a ruler the distance between (or the overlap of) the middle fingers behind the back [28].c. HRQoL. This will be assessed using the 36-Item Short-Form Survey (SF-36) [29] in its Portuguese version [30,31], a 36-question tool, which results in 8 dimensions of health status (physical function, physical role, bodily pain, general health, vitality, social function, emotional role, and mental health) and 2 summary components (physical and mental). Dimensions and components are scored from 0 to 100, where 0 is the worst state, and 100 is the best.d. PAL. This will be assessed using the International Physical Activity Questionnaire Short Form (IPAQ-SF) [32]. This instrument consists of four questions informing on the frequency (days/week) and duration (minutes/day) of daily walks and activities requiring moderate to vigorous physical exertion, as well as the time (minutes/day) spent on sitting activities on weekdays and weekends. PA will be classified into three categories according to the IPAQ consensus group: sedentary (33].e. Subjective Perception of Effort. This will be assessed through the Borg Rating of Perceived Exertion Scale [34] during the sessions, consisting of 10 items for which participants rate their effort from “not at all” (1) to “maximum” (10).f. Adherence rate. This will be controlled. For this purpose, following previous studies [35,36] the following parameters will be monitored: proportion of participants completing exercise programmes, proportion of exercise sessions attended, average number of exercise sessions completed per week, class attendance expressed as a proportion of participants reaching certain cutoffs, number of weeks in which exercise was undertaken, and proportion of days on which exercise was undertaken. In addition, recommendations from previous studies will be followed to encourage adherence to the programme, including making instructions to subjects simpler and less demanding, addressing cognitive motivational factors such as self-efficacy and health beliefs, offering social support and reinforcement, and providing reminders [37,38].g. Level of satisfaction. This will be evaluated through the Physical Activity Enjoyment Scale (PACES) survey, which consists of 8 items that are scored from 1 to 7 points (where 1 = “I enjoy it”, 7 = “I hate it”, and 4 = “neutral”). The total score will be calculated from the sum of the items, with a maximum possible score of 56 points and a minimum of 8; the higher the score is, the greater the enjoyment is. The Portuguese version will be completed by the participants [24]. 2.8. Statistical AnalysisDescriptive statistics and computations will be performed with SPSS (version 25.0; IBM SPSS Inc., Armonk, IL, USA). Personal data will be kept anonymous.
The normality and homogeneity of data will be checked by applying Kolmogorov– Smirnov and Levene’s tests, respectively. Data will be presented as means and standard deviation (SD) (parametric variables) or median and interquartile range (IR) (nonparametric variables). The independent samples t-test (parametric variables) or the Mann–Whitney U test (non-parametric variables) will be used to determine whether the experimental and control groups were comparable at baseline in terms of participant characteristics. Then, repeated measures of ANCOVA will be applied to analyse the intervention effects on the different dependent variables, adjusted by age and baseline outcomes. Cohen’s d (with a 95% confidence interval) will also be included in the results as the effect size. Effect size thresholds will be interpreted as follows: >0.2, small; >0.5, moderate; >0.8, large [36]. Statistical significance will be computed for the effect of time and the interaction group × time. The alpha level will be fixed at p ≤ 0.05. 3. DiscussionThis project will be the first conducted developing a sensorimotor training programme for 24 weeks using different sensorimotor skills in Portuguese older adults, to test this programme’s effects on HRQoL and fall prevention compared to usual care. Different difficulty levels will be included, facilitating individualisation. This training programme can be applied by multiple agents who might be interested in reaping the benefits of these types of activities, since this training method does not require any specific installation and can be completed indoors or outdoors.
In this sense, Avelar et al. [21] carried out a similar quasi-experimental study, with a similar training period composed of exercise circuits to improve strength, gait, functional reach, and static and dynamic balance, among others. Positive responses in lower limb strength, power, mobility, and static and dynamic balance were found, although the sample was small [20,21,27], compared to the 160 participants expected for our study. Other research [17,18,39] used sensorimotor training programmes on functional capacity and balance for a short time, from two to six weeks. Despite the short period, positive results were obtained concerning balance, mobility, activities of daily living performance, and fall risk. Thus, by improving physical capabilities, fall risk could be lower. Other studies [19,20,21] have applied 12–13 weeks of sensorimotor training, half of what is proposed in this protocol. There were positive results for mobility and balance and an improved ability to produce the maximum and explosive force of leg extensors. Several of these studies developed a short-time practical application [39], had a small size [21], or assessed only one or two sensorimotor abilities [17,18,19,20]. For all these reasons, no studies with consistent results have produced an advance on this topic, bearing in mind that the percentage of old people practising PA is very low [40], so it is essential to promote PA practise, as sensorimotor skills may be deficient.The application of this study is expected to obtain an increase in physical capacities such as strength, flexibility, gait, postural control, balance, and agility. In addition, we are also aiming to improve the participants’ HRQoL and reduce their fall risk. The programme could be applied to public and private entities. In the public sector, the application of active retirement programmes within the services offered by public health programmes exists at a regional level, as is the case of the “Alma Senior” programme, developed in the Municipality of Almada, Portugal, or the “The Exercise Looks After You” programme, developed in Extremadura, Spain, which increases its cost–benefit ratio for all aspects related to HRQoL and fall prevention in this sector. Likewise, the possibility of implementing this training system in different associations can be studied. In the private sector, a focus group study can include the heads of health and sports centres, focusing on the applicability of sensorimotor training in their centres, with the results of the study able to highlight the potential advantages of private sector application.
The Portuguese population has experienced a substantial increase in average life expectancy in the last four decades. During the same period, there has been a progressive increase in health expenditure [41]. Regarding the relationship between ageing and health expenditure, there does not seem to be a consensus in the literature on the effects of ageing on health expenditure. The literature refutes that population age is a major determinant of health expenditure and other factors, thus considering a strong positive correlation between the two variables. This correlation is not confirmed in the majority of econometric analyses that have been developed in the last two decades in the area of health economics [42]. Thus, PA should be considered an essential item for public health, since, if performed regularly, it is considered an important condition for health promotion and the prevention/remediation of chronic diseases, for different age groups [43].Regarding limitations, one of the limitations that will exist for the application of this study is being after/during the COVID-19 pandemic. We must take extra care, by adding space and material for the hygienists, to give greater security to the programme. Travel to the space where the programme will be carried out may also be a limitation, considering that the population under study involves people who no longer travel by car; it may be too far away for them to travel on foot, so there will be increased costs due to the necessity of using public transport.
In the future, it would be interesting to evaluate all age groups, in addition to this age group, such as those who are still actively employed, to have a better perception of what happens throughout life in terms of sensorimotor behaviour, not just during the ageing process. This could result in people being able to act from an early age, to improve the capacities analysed in this study. In addition, it would be interesting to add other clinical variables more related to health, such as blood pressure and cholesterol, because, as reported in other studies [44], there were improvements in these variables in the physical condition of participants. We can also analyse the effects of the programme on the number of medical appointments. Finally, applying a pre-participation physical assessment of the participants by a sports physician would be beneficial.The added value of this study will be the acquired knowledge about sensorimotor training for the elderly, which will present a scientific advancement for PA, HRQoL, and sedentary behaviour prevention. Finally, it will be innovative in creating an intervention manual and a digital library with specific exercises for sensorimotor training, which allow for better adaptation and motor coordination.
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