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Effect of therapeutic touch on pain and anxiety in patients with cancer

Effect of therapeutic touch on pain and anxiety in patients with cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201412094115N3
Enrollment
90
Registered
2015-01-01
Start date
2014-12-22
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

Malignant neoplasms. Malignant neoplasms

Interventions

Intervention 1: Intervention group: Implementation of therapeutic touch for 15 min. Intervention 2: Placebo group: Implementation mimic therapeutic touch, hands hold far from patients body. This do to
Intervention group: Implementation of therapeutic touch for 15 min
Placebo group: Implementation mimic therapeutic touch, hands hold far from patients body. This do to unification placebo and intervention group.

Sponsors

International Branch of Behesti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Informed consent of participants; male patients aged 20 to 65 years; Being conscious; cancer-related pain confirmed by physician; being diagnosed and treated at least for one year; possessing full consciousness and mental health; no history of depression and anxiety before the diagnosis; being in remission stage; no plan for surgery as treatment; no history of using therapeutic touch. Exclusion criteria: Unwillingness to continue participation in the study; use of other methods of alternative medicine during study; need for surgery and invasive diagnostic procedures during study; painful events (accident, acute illness) leading to stress and anxiety during the study; marked change in the dosage of pain medication used (ordered by the physician or by the patient); deterioration of patient health status leading to inability to continue the treatment.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Before and after intervention, after 7th section. Method of measurement: Brief Pain Inventory(BPI).;Anxiety. Timepoint: Before and after intervention, 4th section. Method of measurement: Zungs Self rating Anxiety Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmir Tabatabaee

International Branch of Behesti University of Medical Sciences

tabatabaei.amir@gmail.com+98 21 8820 9020

Outcome results

None listed

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