Electronic Confirmed Versus Conventional Consenting Process: A Randomized Controlled Trial

Study group I (e-confirmed consent only) will receive an electronic invitation to complete the consent process electronically.The COMRADE questionnaire (our primary outcome) will be obtained prior to the initiation of the traditional consent (as in control group).

The study group II will undergo the same intervention as group II but the COMRADE survey questionnaire will be obtained after the paper consent

Subject will go through the consenting process at the day of surgery at the preop visit as standard in our institution only.