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The effect of acupressure on severity of pain and anxiety

Clinical trials The effectiveness of acupressure on pain and anxiety in cancer patients undergoing bone marrow aspiration and biopsy

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016080229159N1
Enrollment
90
Registered
2017-04-27
Start date
2016-12-10
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

neoplasm. Malignant neoplasms

Interventions

Intervention 1: In the experimental group, acupressure will be applyin “Hugo” point or LI4 which is located in the hand, between the first and second metacarpal bones and the seventh heart or He7 whi
In the placebo group, the acupressure will be performed on the same points at a distance of 1.5 cm from the main points,for 1 minute to will be done symmetrically on both hands that these points will
Control group, No procedure will be performed in the control group.
In the experimental group, acupressure will be applyin “Hugo” point or LI4 which is located in the hand, between the first and second metacarpal bones and the seventh heart or He7 which is located in

Sponsors

Vice Chancellor for research of Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria:Having a pathology confirms the person with cancer; Having full consciousness; Age 18 to 65 years years; Avoiding the use of anxiolytic and analgesic medications 12 hours before the procedure; No barrier in place Acupressure such as IV line, ulcer at the site of compression; Bone marrow biopsy is done for the first time;The lack of visual impairment to see a visual scale for pain intensity; Having reading and writing literacy needed for completing the questionnaire; having no experience or knowledge about acupressure. Exclusion criteria: the platelets level decreases to less than 100000 mg/dL, any problem or accident happens during the biopsy and unwillingness for cooperation to be continued.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Before biopsy, during biopsy, immediately after the biopsy. Method of measurement: vas(Visual Analogue Scale).;Anxiety. Timepoint: Before and after biopsy. Method of measurement: Spielberger questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Akbar Moghadamnia

Babol University of Medical Sciences

Moghadamnia@yahoo.com+98 11 3219 9592

Outcome results

None listed

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