GIFT Institute of Integrative Medicine, Pisa, Italy.
Aplysia, Education Programme Partner with University of Pisa, Florence, Padua, MIUR, Pisa, Italy.
Am J Clin Hypn. 2022 Jan;64(3):223-238. doi: 10.1080/00029157.2021.1954872.
The assumption that hypnotic analgesia produces placebo effects is controversial. The cognitive dimension that can distinguish hypnosis from placebo analgesia has been suggested as hypnotic susceptibility. The aim of this study is to investigate the role of the relationship between patient and therapist, assumed to produce the placebo effect, in the clinical context of hypnotic treatment for pain. Seventy subjects were given hypnosis administered by the therapist in person (Group A) and 37 practiced self-hypnosis (Group B) for 8 weeks. The Somatosensory Amplification Scale (SSAS), Stanford hypnotic susceptibility scale type A, Cold pressor test (CPT) and SCL-90 were administered at baseline, and Italian Pain Questionnaire (IPQ) dimensions were used as outcome measures. The SSAS did appear to reflect the efficacy of hypnotic analgesia in all pain variables explored, but only in Group B. An improvement in pain intensity and all IPQ dimensions were found at 8 weeks. In particular, an improvement in the affective dimension of pain, with a medium-high effect size (η2 = .774), was recorded after hypnotic analgesia, with the outcome being better in Group A than in Group B ( = .001). This outcome was independent of hypnotic susceptibility in both groups. Considering our hypothesis that, given the administration of the same suggestions, the therapist could promote the placebo response, contributing to the improvement in the affective dimension of pain outcome, which exhibited a response to the hypnotic treatment independently of hypnotic susceptibility.
认为催眠镇痛产生安慰剂效应是有争议的。被认为能将催眠与安慰剂镇痛区分开来的认知维度被认为是催眠感受性。本研究旨在探讨在催眠治疗疼痛的临床环境中,假设能产生安慰剂效应的医患关系在其中所起的作用。70 名被试接受了由治疗师亲自实施的催眠(A 组),37 名被试接受了 8 周的自我催眠(B 组)。在基线时使用体感放大量表(SSAS)、斯坦福催眠感受性量表 A 型、冷加压试验(CPT)和 SCL-90,使用意大利疼痛问卷(IPQ)的维度作为结果测量。SSAS 似乎确实反映了催眠镇痛在所有探索的疼痛变量中的疗效,但仅在 B 组中如此。在 8 周时,疼痛强度和所有 IPQ 维度均有所改善。特别是,在催眠镇痛后,疼痛的情感维度得到了改善,具有中高强度的效应量(η2=.774),A 组的结果优于 B 组(=.001)。这一结果在两组中均与催眠感受性无关。考虑到我们的假设,即给予相同的暗示,治疗师可以促进安慰剂反应,有助于改善疼痛结果的情感维度,这一反应独立于催眠感受性对催眠治疗产生反应。