Long Term Effects of Inspiratory Muscle Training in Cerebral Palsy

Study design The study was a controlled, randomised, double-blind trial and with allocation concealment. The Bioethics Committee of the University of Salamanca affirms that the study meets ethical requirements for its execution (registry number 678)

Participants Institutionalized adults with CP aged between 35 and 64 years were included in the study, they were all members of ASPACE Salamanca. 38 patients with CP were selected to participate in the study. 27 participants were voluntarily recruited to participate in respiratory training and randomly distributed in the High Intensity Training Group (HIT) or Low Intensity Training Group (LIT).

Exclusion criteria

the presence of a respiratory disease in the previous month, inability to understand assessment tests or intervention or hemodynamic alterations (heart rate > 150 beats per minute (bpm), systolic blood pressure > 140 millimeters mercury (mmHg) or diastolic blood pressure > 90 mmHg).

The sample size was established by sampling calculation done from collected during a pilot study with 10 volunteers, which determined a minimum of 10 patients for each group to perceive differences of 12 cmH2O for MIP, power of 80%, security of 95%.

Procedures and Measures of Outcomes Elderly people with cerebral palsy were randomly allocated, via computerized random assignment, to either a high intensity intervention group or a low intensity intervention group. The professional that collected the data and the participants were unaware of group assignment. Before (pre-intervention) and after (post-intervention) inspiratory muscle training, respiratory muscle strength and pulmonary function were evaluated. Once the intervention period phase ended, 3 more evaluations of the same parameters were mare, the first at 4 weeks, the second at 12 weeks and the third at 24 weeks after finishing IMT.

Primary outcome The primary outcome was respiratory muscle strength, measured pre-IMT, post-IMT and 4, 12 and 24 weeks after finishing IMT intervention. It was evaluated through maximum inspiratory pressure (MIP) and maximum expiratory pressure (MEP) using a pressure measurer (Elka PM-15, Laboliser, S.A., Barcelona, Spain), from residual volume and total lung capacity, severally. Each measure was expressed in millibars and turned into centimeter of water, reference unit, (cm H2O) (1 mbar = 1.01973 cm H2O), according to recommendations of the American Thoracic Society/European Respiratory Society (ATS / ERS) [24]. Each test was repeated 3 times or until 2 valid results were obtained (difference less than 5%). A rest time of 1 minute was respected between efforts to prevent short-term respiratory muscle fatigue. The highest value was selected. MIP was evaluated every 2 weeks to graduate the load of the device training.

Secondary outcome The secondary outcome was pulmonary function, measured pre-IMT, post-IMT and 4, 12 and 24 weeks after finishing IMT intervention. The data collected were forced expiratory volume in 1 second (FEV1) and peak expiratory flow (PEF). It was measured using the peak flow device (Asma-1, Vitalograph Ltd, Buckingham, England) that expresses the results of FEV1 in liters (L) and PEF in liters per minute (L/min), according to the guidelines of the ATS/ERS.

Experimental Protocol Inspiratory muscle training was carried out with a pressure threshold device (Treshold IMT, Philips-Respironics, Pittsburg, PA, USA). Threshold IMT provides consistent and specific pressure for inspiratory muscle strength and endurance training, regardless of how quickly or slowly patients breathe. This device incorporates a flow-independent one-way valve to ensure consistent resistance and features an adjustable specific pressure setting (in cm H2O) to be set by a healthcare professional. When patients inhale through Threshold IMT, a spring-loaded valve provides resistance. Before training began, the participants and primary caregivers completed one-session familiarization with a specialist to learn how to operate the device.

Adult people with cerebral palsy carried out the training program for 8 weeks, 1 session every day, 5 days a week. The participants performed 10 series of 1 minute with 1-minute rest between them.

The High Intensity Training Group (HIT) received IMT at 40% of MIP, the training load was set each 2 weeks to keep 40% of MIP. The Low Intensity Training Group (LIT) received IMT at 20% of MIP, following the same rules as HIT.

The training protocols of the two groups were developed by a specialist in respiratory therapy and all sessions with IMT were supervised by their main caregiver, therefore adherence to the program was controlled, as well as possible unwanted effects (increased fatigue, breathing problems, dizziness or sickness).

During the intervention period, both groups continued with their usual activity, receiving physiotherapy treatment for 45 minutes per day, 2 days per week. No participants received any other treatments.

After finishing the 8-week intervention period with IMT, CP patients stopped training with IMT and continued with their daily normal activities. During the following 24 weeks (without IMT), three evaluations of the respiratory parameters analyzed in the trial were made (MIP, MEP, FEV1, PEF). The first evaluation was made 4 weeks after the intervention was completed, the second 12 weeks and the third 24 weeks after finishing IMT.

Inclusion criteria

• Institutionalized adults with cerebral palsy

Exclusion criteria

• The presence of a respiratory disease in the previous month
• Inability to understand assessment tests or intervention
• Hemodynamic alterations (heart rate > 150 beats per minute (bpm), systolic blood pressure > 140 millimeters mercury (mmHg) or diastolic blood pressure > 90 mmHg).