Male and female adults were recruited to participate in this study from a University staff population of approximately 1700 individuals. Inclusion criteria required that participants were sedentary (<1 h of moderate-intensity exercise/week), did not smoke, had no current or recent (within 3 months) musculoskeletal injury or recent URT infection. Recruited participants were also classified in the BMI range of 27-35 kg.m-2 (overweight: 25-29.9; obesity: 30+) and had not been exposed to hypoxic conditions within the previous 6 months prior to the start of the study (see Table 1 for anthropometric data of the sample). Written informed consent was obtained from all participants. This study was carried out in accordance with the Declaration of Helsinki. Ethical approval was received from the School of Applied Sciences Ethics Committee (SAS1822). This study compared two separate groups of adults who were classified as overweight or obese, whereby, half of the participants completed their sessions in hypoxic conditions (FiO2 = 13.0%, equivalent to ~3500 m elevation above sea level, HYP; n = 8), and the other half completed their sessions in normoxic conditions (sea level, NOR; n = 8). Participants were randomly allocated to training conditions through simple randomization. Participants completed eleven separate visits across three consecutive weeks and were instructed to maintain their normal daily habits in terms of activity, diet, social interactions and sleep patterns. The first session (visit 1) consisted of eligibility determination, familiarisation with the measures and treadmill walking (Pulsar, h/p/cosmos, Germany), and identification of the walking velocity associated with a RPE of 14, as described previously (Hobbins et al. 2019). Within 72 h, participants returned to the lab for pre-testing (visit 2), which consisted of assessment of anthropometrics (body mass and stature), physiological responses (blood pressure), exercise-related sensations (perceived mood change and exercise self-efficacy) and functional fitness (6-min walk test). After 24-72 h, participants undertook the first of eight supervised 60-min self-paced interval-walking training interventions. Visits 4–10 involved the remainder of the 8 training sessions, which were completed within a 2-week period. Within 72 h of the final perceptually regulated interval walking session, participants returned to the lab (visit 11) for post-intervention testing. Testing and training environments were maintained at 23iC and 45% relative humidity. The eight supervised 60-min perceptually regulated interval-walk sessions were completed across two consecutive weeks in a commercial gym (Academy of Sport, London South Bank University). Each session began with a 5-min warm up at 3.0 km·h-1 on the treadmill (Fusion Run Series3, Pulse Fitness, UK). A facemask connected to a portable hypoxic generator (see below) was then attached and remained in place for the entire session. During all sessions, the first 30 s of each 2-min interval began at the participants’ perceptually regulated walking velocity (RPE = 14) identified at visit 1. Following this, participants were able, every 30 s, to decide if and how treadmill velocity needed to be altered (i.e., increased or decreased by 0.5, 1.0 or 1.5 km·h-1, or maintained) to ensure maintenance of an RPE of 14 whilst walking. The facemask (Altitude Training Mask, Hypoxico Altitude Training Systems, USA) was connected via corrugated plastic tubing to a hypoxic generator (Everest Training Summit II, Hypoxico Altitude Training Systems, USA) to create hypoxic conditions. The hypoxic level provided in this study was an FiO2 13.0% (simulated altitude of ~3500 m), while the total hypoxic exposure corresponded to exactly 480 min for those in the HYP group. Participants in the normoxic group were blinded to the condition by being connect to the same hypoxicator system set at sea level equivalent FiO2 (21%). Treadmill velocity, HR (M400, Polar, Finland) and arterial oxygen saturation (SpO2) (iHealth Air, iHealthLabs, USA) were recorded every 30 s during interval walking. Before each session, perceived recovery was assessed in response to a numeric scale, ranging from 0 being ‘very poorly recovered’ to 10 being ‘very well recovered’ (Laurent et al. 2011). Perceived motivation was assessed via a 20 cm visual analog scale, with 0 being ‘not very motivated’ (white colored) and 20 being ‘very motivated’ (black colored) (Crewther et al. 2016). Immediately after each training session, perceived breathlessness and limb comfort were determined in response to a numeric scale ranging from 0 being ‘nothing at all’ to 10 being ‘very, very severe’ (Ward and Whipp, 1989), whilst perceived pleasure was assessed via a 20-cm visual analog scale ranging from 0 being ‘not very pleasant’ (white colored) and 20 being ‘very pleasant’ (black colored). Participants arrived at the lab following an 8-h fasting period (water exempt). Stature and body mass, and subsequently BMI, were assessed using an electric stadiometer (220, Seca GmbH, USA). After 10 min of rest, participants were asked ‘how are you feeling right now?’ and instructed to verbally specify a number on an 11-point scale anchored ‘very bad’ (-5) up to ‘very good’ (+5) for perceived mood state (Hardy and Rejeski, 1989). Exercise self-efficacy was determined by participants completing a six item, 11-point Likert scales (Smith et al. 2012). Blood pressure (systolic and diastolic) was assessed via an automated pressure cuff (Omron M4, Omron, Japan) attached, secured and inflated around the upper arm, level with the heart. Participants completed a standardised warm up (5 min at 3 km·h-1) before a functional fitness test involving 6 min of perceptually regulated continuous walking in normoxic conditions. The treadmill velocity was set at 50% of their self-selected walking velocity, and participants stepped on whilst the velocity was increased to their velocity associated with an RPE of 14 within 10 s. Participants were instructed to ‘walk as far as possible in six minutes without running or jogging’. They were able to maintain the velocity or increase/decrease it by 0.5, 1.0 or 1.5 km·h-1 every 30 s. Following completion of the 6-min period the total distance covered was recorded (Gibson et al. 2015). Preliminary analysis (paired-sample, equal variance t-test) was carried out to determine whether pre-tests measurements were statistically significantly different between HYP and NOR. If statistical differences were found, data collected during and post-training were normalized to the pre-training measurement. Velocity, HR and SpO2 were averaged across each 60-min session. Velocity, HR and exercise-related sensations recorded during sessions 2-8 were calculated as a percentage change from session 1 (100%) due to differences in the initial velocity deemed equal to RPE 14 between HYP and NOR. Data are presented as mean ± standard deviation. A t-test was used to determine any statistically significant differences in the absolute velocity, HR, SpO2, perceived recovery, motivation, breathlessness, limb discomfort and pleasure values (averaged across the session) during session 1. A two-way repeated-measures ANOVA was used to investigate the main effect of condition (hypoxia vs. normoxia), time (pre-training vs. post-training or session 1 vs. 2, 3, 4, 5, 6, 7 and 8) and the condition × time interaction. A Bonferroni post hoc multiple comparison was performed if a significant main effect was observed. Effect sizes were described in terms of partial eta-squared (ηp2, with ηp2 ≥ 0.06 representing a moderate effect and ηp2 ≥ 0.14 a large effect). All statistical calculations were performed using SPSS statistical software (IBM Corp., Armonk, NY, USA). The significance level was set at p < 0.05. |