| Literature DB >> 29186070 |
Sabine C Koch1,2, Helena Rautner3.
Abstract
In the context of embodiment research, there has been a growing interest in phenomena of interpersonal resonance. Given that haptic communication is particularly under-researched, we focused on the phenomenon of embracing. When we embrace a dear friend to say good-bye at the end of a great evening, we typically first employ smooth and yielding movements with round transitions between muscular tensing and relaxing (smooth, indulging rhythms), and when the embrace is getting too long, we start to use slight patting (sharp, fighting rhythms with sharp transitions) on the back or the shoulders of the partner in order to indicate that we now want to end the embrace. On the ground of interpersonal resonance, most persons (per-sonare, latin = to sound through) understand these implicit nonverbal signals, expressed in haptic tension-flow changes, and will react accordingly. To experimentally test the hypothesis that smooth, indulgent rhythms signal the wish to continue, and sharp, fighting rhythms signal the wish to separate from an embrace, we randomly assigned 64 participants, all students at the University of Heidelberg, to two differently sequenced embrace conditions: (a) with the fighting rhythm at the end of the sequence of two indulgent rhythms (Sequence A: smooth-smooth-sharp); and (b) with the fighting rhythm between two indulgent rhythms (Sequence B: smooth-sharp-smooth). Participants were embraced for 30 s by a female confe-derate with their eyes blindfolded to focus on haptic and kinesthetic cues without being distracted by visual cues. They were instructed to let go of a handkerchief that they held between the fingers of their dominant hand during the embrace, when they felt that the embracer signaled the wish to finish the embrace. Participants significantly more often dropped the handkerchief in the phase of the fighting rhythm, no matter in which location it occurred in the embrace sequence. We assume that we learn such rhythmic behaviors and their meaning from the beginning of life in the communication with caregivers and meaningful others. Some are universal and some are quite idiosyncratic. Infants seem to be highly sensitive to the dynamic nuances presented to them, demonstrating a high capacity for embodied resonance and a high behavioral plasticity. Such adaptive mechanisms are assumed to lay the foundations of family culture (including the degree to which nonverbal cues are attended to, the communication of taboos, etc.) and larger culture, and may also play an important role in interpersonal attraction and aesthetic experience.Entities:
Keywords: Kestenberg Movement Profile (KMP); embodiment; haptic communication; interpersonal resonance; movement analysis; movement qualities; movement rhythms; musicality; rhythmicity; vitality affects
Year: 2017 PMID: 29186070 PMCID: PMC5746689 DOI: 10.3390/bs7040080
Source DB: PubMed Journal: Behav Sci (Basel) ISSN: 2076-328X
Figure 1Prototypic Tension-Flow Rhythms of the Kestenberg Movement Profile (KMP; Kestenberg, 1975/95) [2]. Note: Tension-flow rhythms are the rhythmic changes between tension and relaxation in the body of an individual; they are notated on paper, yielding a continuous tension-flow line on a timeline from left to right; downward writing indicates moving into higher tension; upward into lower tension (by convention); they are similar to Stern’s concept of vitality affects (2012) [45], but more on the active side (and thus more directly connected to control, self-efficacy, and self-regulation); in the embrace study, we used the sucking, swaying, and biting rhythm (figure adapted from Koch & Sossin, 2012) [5].
Figure 2The two embrace conditions (the first rhythm was a sucking rhythm in both sequences, the second either a swaying (A) or a biting rhythm (B); and the last either a biting (A) or a swaying-rhythm (B); the biting rhythm was employed, because it was the most natural sharp rhythm in embraces, according to our naturalistic pre-study); each sequence lasted 30 s and consisted of three rhythms; each phase lasted 10 s.
Descriptive Statistics of Time of Signal, Phase of Drop, and Affect Change (N = 60).
| Sequence | Mean | SD | N | |
|---|---|---|---|---|
| A: sm-sm-sh | 23.13 | 4.85 | 31 | |
| B: sm-sh-sm | 17.17 | 5.72 | 29 | |
| A: sm-sm-sh | 2.74 | 0.51 | 31 | |
| B: sm-sh-sm | 2.24 | 0.43 | 29 | |
| A: sm-sm-sh | 0.28 | 0.52 | 31 | |
| B: sm-sh-sm | 0.28 | 0.57 | 29 |
Note: SD = Standard Deviation; N = Number of participants; Time of Signal: time measured from onset of embrace to drop of the handkerchief; Phase of Signal: 1 = Phase 1 (smooth rhythm), 2 = Phase 2 (smooth in Sequence A; sharp in Sequence B); 3 = Phase 3 (sharp in Sequence A, smooth in Sequence B), means low, because of error drops (e.g., in Phase 1); Affect Change = Posttest-Pretest on MBAS-Scale (Koch & Müller, 2007) [72]; sm = smooth rhythm; sh = sharp rhythm; Degrees of freedom = 1.
Crosstab for Phase of Signal.
| Rhythms Sequence | ||||
|---|---|---|---|---|
| Sequence A | Sequence B | Total | ||
| Phase of Signal | Phase 2 (s 10–20) | 6 | 22 | 28 |
| Phase 3 (s 20–30) | 24 | 7 | 31 | |
| Total | 30 | 29 | 59 | |
Note: There was one participant in both trials that already signaled in the first phase and one participant that signaled only after the last phase; these two participants (both in the condition Sequence A) were taken out of the analysis, resulting in N = 59 (30 vs. 29), from these 46 persons (78%) understood the signal, and 13 did not, according to the results for phase of signal.
Inferential Statistics of Time of Signal (Drop of Handkerchief) and Affect Change (N = 60).
| Sequence | ||||
|---|---|---|---|---|
| A: sm-sm-sh | 18.90 | 0.000 | 0.25 | |
| B: sm-sh-sm | ||||
|
| A: sm-sm-sh | 0.007 | 0.934 | 0.00 |
| B: sm-sh-sm |
Note: SD = Standard Deviation; N = Number of participants; Time of Signal: measured from onset of embrace to drop of the handkerchief; Affect Change = Posttest-Pretest on MBAS-Scale (Koch & Müller, 2007) [72]; sm = smooth rhythm; sh = sharp rhythm; Degrees of freedom = 1.
Figure 3Times from Onset of Embrace to Signal Detection by Gender (N = 60). Note. Sequence A: smoot-smoot-sharp; Sequence B: smooth-sharp-smooth; the difference for time of signal was significant with F(1, 60) = 18.90, p = 0.000, eta2 = 0.25; the difference in time of signal between men M = 20.21 (SD = 5.84) and women M = 20.29 (SD = 6.16) was not significant, F(1, 59) = 0.07, p = 0.789, eta2 = 0.00.
F-, p- and eta2-values for the three possible computational ways for the effect of rhythm sequence on the time in which the handkerchief was dropped.
| Signal I (preliminary trail) | 48 (26/22) | 21.31 vs. 15.73 | 4.28 vs. 5.48 | 17.70 | 0.000 | 0.29 |
| Signal II (main trail) | 51 (29/22) | 23.72 vs. 18.09 | 4.39 vs. 6.05 | 14.06 | 0.000 | 0.23 |
| Signal III (n = 8 from I, and n = 52 from II) | 60 (31/29) | 23.13 vs. 17.17 | 4.85 vs. 5.72 | 18.53 | 0.000 | 0.25 |
Note. N = number of participants; A = Sequence A (smooth-smooth-sharp); B = Sequence B (smooth-sharp-smooth sequence); M = mean; SD = Standard Deviation; F = F-value (statistics of group differences); p = p-value (probability/significance level) and eta2 = effect size; Signal I = time of drop of handkerchief in preliminary trial (first embrace); Signal II = time of drop of handkerchief in main trial (second embrace); Signal III = 52 times of drop of handkerchief from Signal II, & eight replaced by time of drop of handkerchief from Signal I; final analysis with the data from Signal III.