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Effect of hypnotherapy on background pain and pain anxiety of men with burn injuries hospitalized in burn ward

Effect of hypnotherapy on intensity and quality of background pain and pain anxiety of men with second and third degree burn injuries: A blinded, randomized clinical trial with control group

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016100830214N1
Enrollment
60
Registered
2016-11-11
Start date
2016-10-31
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

Condition 1: Burn of second degree. Condition 2: Burn of third degree. Burn of second degree, body region unspecified Burn of third degree, body region unspecified

Interventions

Intervention 1: Control group: In this group four sessions of hypnosis will be done. Needed time for hypnosis sessions will range from 15 minutes to one hour depending on the hypnotizability. Differen
Treatment - Other
Control group: In this group four sessions of hypnosis will be done. Needed time for hypnosis sessions will range from 15 minutes to one hour depending on the hypnotizability. Different induction tech
Intervention group: In this group four sessions of hypnosis will be done. Needed time for hypnosis sessions will range from 15 minutes to one hour depending on the hypnotizability. Different induction

Sponsors

Research Vice President of Urmia University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients should have diagnosis of burn injury and be hospitalized in hospital; men who are between 18 and 50 years old; passing the emergency phase of burn and being in later phases; second and third degree burn injuries with total body surface area ranging from 5 to 40 percent; Farsi and Azeri speakers; having no problem in hearing and vision; having no diagnosis of psychosis, epilepsy, drug abuse or mental problems; having no history of hypertension or diabetes. Exclusion criteria: unwillingness of participation in research; leaving the ward for any reason such as transferring to other hospitals or intensive care unit; discharge or death; wound infection with positive culture; having any out of routine procedure.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Intensity of pain. Timepoint: Before intervention, after second and also forth session of intervention. Method of measurement: Visual analogue scale.

Secondary

MeasureTime frame
Quality of pain. Timepoint: Before intervention, after second and forth session. Method of measurement: Short form of McGill pain questionnaire.;Pain Anxiety. Timepoint: Before intervention, after second and forth session. Method of measurement: Burn Specific Pain Anxiety Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHossein Jafarizadeh

Urmia University of Medical Sciences

JAFARIZADEH@UMSU.AC.IR+98 44 3193 7224

Outcome results

None listed

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