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The effect of Benson’s relaxation technique on depression, anxiety, and quality of life of caregivers

A clinical trial for determination of the effect of Benson’s relaxation technique on depression, anxiety, and quality of life of caregivers of patients with cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20100403003618N7
Enrollment
50
Registered
2019-07-04
Start date
2019-06-22
Completion date
Unknown
Last updated
2020-05-18

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

Conditions

Condition 1: Depression. Condition 2: Anxiety. Condition 3: Quality of life. Major depressive disorder, single episode, mild Generalized anxiety disorder Malignant neoplasm without specification of site

Interventions

Intervention 1: Intervention group: Benson's relaxation technique will be performed once a day (20 minutes) for six weeks. Intervention 2: Control group: The control group will not receive interventio

Sponsors

Kashan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 59 Years

Inclusion criteria

Inclusion criteria: Caring for a patient with cancer at the time of the study (i.e. a spouse, a child, a father, or a mother). Age between 20 and less than 60 years. Fluency and ability to read and write in Persian language. Willingness to participate in the study and signing the informed consent form. Not receiving antidepressants and anxiolytic medications at the beginning of the study. Having mild or higher anxiety and depression based on Beck’s depression and the Spielberger State-Trait Anxiety Inventories. Having no known cognitive impairment (to this end, the individual, and the patient will be questioned if any physician made him/her a medical diagnosis of mental disorders such as amnesia and Alzheimer disease?)

Exclusion criteria

Exclusion criteria: A caregiver’s decision to withdraw from the study. Getting any acute illness or conditions requiring medical attention during the study. The occurrence of a critical condition for the caregiver (such as getting an acute illness, being hospitalized, being divorced) so that his/her quality of life is affected. Doing the recommended intervention for less than 5 sessions in a week. Death of a caregiver.

Design outcomes

Primary

MeasureTime frame
Depression. Timepoint: Before the intervention, the end of the sixth week of intervention, and also four weeks after the end of the intervention. Method of measurement: The Beck Depression Inventory.;Anxiety. Timepoint: Before the intervention, the end of the sixth week of intervention, and also four weeks after the end of the intervention. Method of measurement: The Spilberger Inventory.

Secondary

MeasureTime frame
Quality of life. Timepoint: Before the intervention, the end of the sixth week of intervention, and also four weeks after the end of the intervention. Method of measurement: The Caregiver Quality Of Life index-Cancer scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBahareh Ebrahimi

Kashan University of Medical Sciences

bahar.nurse.2015@gmail.com+98 31 5552 3879

Outcome results

None listed

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