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Effect of hypnosis to reducing the pain in head and neck cancer during radiotherapy

Effect of hypnosis to reducing the pain in head and neck cancer:randomize control trials

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
TCTR
Registry ID
TCTR20160905001
Enrollment
Unknown
Registered
2016-09-05
Start date
2015-03-08
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

cancer pain Hypnosis&#44

Interventions

On the first day of admission&#44
the patients were assessed for the level of pain by visual analogue scale (VAS) by the research assistant three times in 24 hours. A list of patient with a pain score of four or greater was given to t
the research assistant assessed the level of pain at 6.00 am&#44
10.00 am&#44
14.00 pm and 18.00 pm&#44
for 4 days.,On the first day of admission&#44
the patients were assessed for the level of pain by visual analogue scale (VAS) by the research assistant three times in 24 hours.The next day&#44
for 4 days. The researchers were encouraged to establish a relationship whilst explaining the objectives and the project in details. The patients were given time for inquiries before the consent was o
the researchers evaluated the hypnotic ability of the volunteers in the treatment group by Stanford hypnotic susceptibility scale form C. On the third day&#44
the participants in the treatment group were provided an introduction to the hypnosis exploring differences with the patient and practices of the hypnosis. On the fourth day&#44
the patient underwent hypnotherapy which took 20 minutes.
No Intervention,hypnosis

Sponsors

Community Medicine, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand
Lead Sponsor
N/A,N/A
Collaborator

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: The participant were head and neck cancer patients aged between 40 -70 years, with a score of four on visual analogue scale (VAS) at the first admission. Assessment was performed for vulnerability to hypnosis with Stanford hypnotic susceptibility scale form C with high levels of pain more than or equal to five

Exclusion criteria

Exclusion criteria: diagnosis that are psychosis, somatoform disorder, depression,adjustment disorder and end of life

Design outcomes

Primary

MeasureTime frame
pain score 4 days visual analogue scale

Secondary

MeasureTime frame
No No No

Countries

Thailand

Contacts

Public ContactKanitta Thuma

Srinagarind Hospital

kanthuma22@gmail.com+669-567-05472

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026