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Investigation the Effectivness of Snoezelen room on anxiety and Physiological indicators of anxiety of cancer patients during chemotherapy

Investigation the Effectivness of Snoezelen room on anxiety and Physiological indicators of anxiety of cancer patients during chemotherapy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2012072910442N1
Enrollment
Unknown
Registered
2012-12-24
Start date
2012-06-17
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

Anxiety. Other anxiety disorders

Interventions

Intervention 1: Intervention groups: designing Snoezelen room, seting up fish pool, lighting to wall, aromatherapy with ?lavender or orange, relaxing or nature music. Intervention 2: control group: n
Treatment - Other
Intervention groups: designing Snoezelen room, seting up fish pool, lighting to wall, aromatherapy with ?lavender or orange, relaxing or nature music

Sponsors

Tehran University of Medical Sciences. Faculty of ?Nursing and Midwifery
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria:Their age is 18 to 65 years old; They don’t have chronic and high risk diseases such as diabetes;There is no Visually impaired to the extent that be able to see player pictures on the walls of the room;? History of psychological problems with anxiety disorders is not known; History of sleeping and sedative drug use is not known; There is no addiction to drug and Strong analgesic;There is no hypertension or taking hypertension meditation; There is no Hearing problem that prevents the music is not heard; Not medical personnel or university education in field of medical sciences and psychology; Have the ability to smell (the sense of smell is not affected by extreme cold)? Exclusion criteria:? Occurring any crisis within four weeks; Unwillingness to continue participation in the study at any time of the study; Any sudden drastic changes in vital signs;any drug side effects in patients; severe allergy to perfume fragrances and essential oils.?

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Anxiety. Timepoint: 1 hours before and after intervention ?. Method of measurement: spielberger questionairre.

Secondary

MeasureTime frame
Pulse rate. Timepoint: 1 hours before and after intervention ?. Method of measurement: With stopwatch for one minute.;Blood presure. Timepoint: one hour before and after intervention. Method of measurement: Analog sphygmomanometer.;Respiratory rate. Timepoint: one hour before and after intervention. Method of measurement: With stopwatch for one minute.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParya Taheri Bandari

Scool of Nursing and Midwifery,Tehran University of Medical Sciences

p-taheri@razi.tums.ac.ir+98 21 6692 7171

Outcome results

None listed

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