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Table 1 Treatment sessions

From: Efficacy of capacitive resistive monopolar radiofrequency in the physiotherapeutic treatment of chronic pelvic pain syndrome: study protocol for a randomized controlled trial

 

Intervention group (IG)

Control group (CG)

Session 1

Review of the information sheet and signing of informed consent.

Collection and recording of baseline data (age, sociodemographic data, clinical data, and medical and surgical history). Self-completion of tests (VAS, SF-12, TSK-11, and PCS).

Application of physiotherapeutic techniques with activated CRMRF.

Explanation of the theory of pain and health education.

Application of physiotherapeutic techniques with deactivated CRMRF.

Explanation of the theory of pain and health education.

Session 2–5

Session protocol:

• Registration of possible discomfort or adverse events perceived by the patient.

• Application of physiotherapeutic techniques with activated CRMRF.

• Pain education clarifications

Session protocol:

• Registration of possible discomfort or adverse events perceived by the patient.

• Application of physiotherapeutic techniques with deactivated CRMRF.

• Pain education clarifications

Session 6

Collection of VAS, SF-12, TSK-11, and PCS tests.

Session protocol (as described in session 2–5)

Session 7–9

Session protocol (as described in session 2–5)

Session 10

Session protocol (as described in session 2–5)

Assessment of VAS, SF-12, TSK-11, PCS tests, evolution of the pathology, and referral (if required).