Healthy Volunteers Clinical Trial
Official title:
Effectiveness of Mixed Reality With the Hololens System Versus Conventional Cervical Exercise Program for Asymptomatic Subjects. Crossover Pilot Study
The study design is a cross-over pilot study with 15 asymptomatic subjects. There will be 2 groups, mixed reality group and conventional cervical exercise program. Both groups received 2 sessions per week with an interval of 48 hours between them during 3 consecutive weeks.
The study design is a cross-over pilot study. The study was approved by the ethical committee
of the Centro Superior de Estudios Universitarios La Salle. People were recruited by referral
from different places of the local community of Madrid according to the CONSORT statement
(Consolidated Standards of Reporting Trials). Three assessors were trained during 300 minutes
about how to perform the measurements (Investigator A) and the concerned intervention to each
group (Investigator B and C). The whole procedure was conducted in the Centro Superior de
Estudios Universitarios La Salle. After meeting the eligibility criteria for the study,
participants were randomly allocated by an external investigator to one of the two groups:
- Mixed reality group
- Conventional Exercise group
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