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Tanscutaneous electrical nerve stimulation (TENS), acupressure and chemotherapy-induced nausea and vomiting.

Comparative study of transcutaneous electrical nerve stimulation (TENS) and acupressure on chemotherapy-induced nausea and vomiting.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20100618004203N14
Enrollment
120
Registered
2018-01-02
Start date
2017-12-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Cancer. Malignant neoplasms, stated or presumed to be primary, of specified sites, except of lymphoid, haematopoietic and related tissue

Interventions

Intervention 1: In the intervention group 1: receiving TENS electric stimulation for 30 minutes at 10 Hz and a 500 msec pulse duration, with a tolerable intensity, to the P6 point of the wrist, once d
Prevention
In the intervention group 1: receiving TENS electric stimulation for 30 minutes at 10 Hz and a 500 msec pulse duration, with a tolerable intensity, to the P6 point of the wrist, once daily, on both ha
In the intervention group 2: Acupuncture wrist band on the P6 point of the wrist, permanently, on both hands for 5 consecutive days.
In the control group 1: receiving placebo TENS electric stimulation for 30 minutes to the P6 point of the wrist, once daily, on both hands for 5 consecutive days.
In the control group 2: ordinary wrist band on the P6 point of the wrist, permanently, on both hands for 5 consecutive days.

Sponsors

Semnan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age over 18 Use of nauseous diets such as cisplatin alone or in combination with other chemotherapeutic agents with the same amount and administration in two cycles of chemotherapy without planning for radiotherapy in cycles At least four times chemotherapy

Exclusion criteria

Exclusion criteria: Having a history of nausea and vomiting for reasons other than chemotherapy;; Taking anti-epithelial (emend) medication Treatment with corticosteroid medications during the cycles Using pacemakers

Design outcomes

Primary

MeasureTime frame
Nausea and vomiting. Timepoint: In hours 1,2,3 and 4 after intervention and 24 hours after beginning of chemotherapy and 5 days later. Method of measurement: checklist and cortilla tool.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Atefeh Aminian Far

Semnan University of Medical Sciences

aminfar@semums.ac.ir+98 23 3365 4180

Outcome results

None listed

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