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P6 acupuncture for the prevention of postoperative nausea and vomiting (PONV) - A study with focus on the patient perspective

P6 acupuncture for the prevention of postoperative nausea and vomiting (PONV) - A study with focus on the patient perspective - Observational study P6 Acupuncture for PONV prophylaxis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00026696
Enrollment
184
Registered
2021-09-23
Start date
2021-09-23
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

observational study R11

Interventions

Group 1: Patients who are about to undergo surgery and have decided to receive perioperative acupuncture for PONV prophylaxis are interviewed with one questionnaire prior to surgery and one after surg
2) "Life-Orientation Tests for Dispositional Optimism and Pessimism", abbreviated LOT-R (Glaesmer et al. 2008)
3) "General Self-Efficacy Expectancy Scale," or SWE (Jerusalem & Schwarzer, 2003). The postoperative questionnaire again includes questions on acceptance ("Credibility/ expectancy questionnaire" accor

Sponsors

Institut für Sportwissenschaften, Abteilung Sportmedizin
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: for patient dataset: a) incapacitated (able to give consent); b) of legal age (age = 18 years); c) anesthesiological management (narcosis) during surgery at one of the study centers; d) ASA I-IV. for clinic staff dataset: direct or indirect patient contact in the context of work activities in the clinic

Exclusion criteria

Exclusion criteria: for patient dataset: (a) Non-consent or inability to perform acupuncture treatment at P6.; (b) Inability to participate in standardized telephone survey; (c) Emergency surgery (reason: it can not be ensured that the survey before the surgery (measurement time 1) will be completed and acute stress prior to emergency surgery does not adequately ensure comparability of results); d) Pregnancy (to avoid interference with pregnancy-related nausea, which is not the research question of this study). for clinic staff dataset: no exclusion criteria

Design outcomes

Primary

MeasureTime frame
To address the main hypothesis, the coping style will be assessed as the primary outcome measure. This personality-related characteristic is measured using the standardized validated psychometric test procedure "Coping Inventory for Dealing with Stressful Situations" (acronym: CISS) (Kälin & Semmer, 2020; German-language adaptation of the Coping Inventory for Stressful Situations). The individual scores on the three scales (task-oriented coping, emotion-oriented coping, and avoidance-oriented coping) are converted into T values by using evaluation tables. This involves a classification into the Gaussian distribution of the representative sample for normative comparison (reference sample). It will be examined whether the values on the above-mentioned three scales deviate significantly from the norm (Gaussian distribution of the reference sample). T-tests are used for this purpose.

Secondary

MeasureTime frame
The survey includes other personality-related characteristics: (a) Life orientation; (b) self-efficacy expectancy. The following secondary outcome describes the link between the hospital setting and acceptance of acupuncture treatment by hospital staff: (a) Dependent variable: expectancy of hospital staff; (b) Independent variables: Characterization of the hospital setting.

Countries

Germany

Contacts

Public ContactKatharina Helbig

SRH Kliniken Landkreis SigmaringenAnästhesie

helbig.anaesthesie@web.de+49 (0)7571 100-2331

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026