Effectiveness of photobiomodulation therapy on pain intensity in postpartum women with nipple or perineal trauma: protocol for a multicentre, double-blinded, parallel-group, randomised controlled trial.

Autor:	Gondim EJL; Universidade Estadual de Campinas, Campinas, Brazil., Nascimento SL; Federal University of Ceara, Fortaleza, Brazil., Gaitero MVC; Universidade Estadual de Campinas, Campinas, Brazil., Mira TAA; Universidade Estadual de Campinas, Campinas, Brazil., Gonçalves AV; Universidade Estadual de Campinas, Campinas, Brazil., Surita FG; Obstetrics & Gynecology, State University of Campinas, Campinas, Brazil surita@unicamp.br.
Jazyk:	angličtina
Zdroj:	BMJ open [BMJ Open] 2023 Dec 14; Vol. 13 (12), pp. e072042. Date of Electronic Publication: 2023 Dec 14.
DOI:	10.1136/bmjopen-2023-072042
Abstrakt:	Introduction: Photobiomodulation (PBM) using low-level laser can affect tissue repair mechanisms and seems promising in reducing pain intensity. However, few studies support the effectiveness of PBM on postpartum period complications, such as nipple and/or perineal trauma and pain, probably due to the low doses used. The primary objective of this study is to analyse the effectiveness of PBM on pain intensity in the nipple and perineal trauma in women in the immediate postpartum period. Secondary objectives are to evaluate the effect on tissue healing and the women's satisfaction. Methods and Analysis: A double-blind, multicentre, parallel-group, randomised controlled trial will be performed in two public referral maternity hospitals in Brazil with 120 participants, divided into two arms: 60 participants in the nipple trauma arm and 60 participants in the perineal trauma arm. Participants will be women in the immediate postpartum period, who present with nipple trauma or perineal trauma and report pain intensity greater than or equal to 4 points on the Numerical Rating Scale for Pain. Block randomisation will be performed, followed by blinding allocation. In the experimental group, one application of PBM will be performed between 6 hours and 36 hours after birth. For the sham group, the simulation will be carried out without triggering energy. Both participants and the research evaluator will be blinded to the allocation group. Intention-to-treat method and the between-group and within-group outcome measures analysis will be performed. Ethics and Dissemination: This research protocol was approved by the Research Ethics Committees of the University of Campinas, Brazil, and of the School Maternity Assis Chateaubriand, Brazil (numbers CAAE: 59400922.1.1001.5404; 59400922.1.3001.5050). Participants will be required to sign the informed consent form to participate. Results will be disseminated to the health science community. Trial Registration Number: Brazilian Registry of Clinical Trials (RBR-2qm8jrp). Competing Interests: Competing interests: None declared. (© Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.)
Databáze:	MEDLINE
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