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Effect of telephone intervention on supportive care needs of patients with cancer

Effect of telephone support on supportive care needs of women with breast cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016102430465N1
Enrollment
62
Registered
2016-12-18
Start date
2016-10-22
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

breast cancer. Malignant neoplasm of breast

Interventions

Intervention 1: Intervention group: Telephone intervention will be performed for a month. The first contact with participants will be done during a week after the first meeting. The researcher will ca
Intervention group: Telephone intervention will be performed for a month. The first contact with participants will be done during a week after the first meeting. The researcher will call patients in t
Control group: The control group will only receive usual care.

Sponsors

Vice Chancellor for Research ofArak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Eligibility to participate was restricted to people diagnosed with cancer; aged between 18-80 years; aware of their diagnosis; are treathed for first round; physically and mentally capable of participating in the study ( the ability to read and write and lack of hearing loss and speech problems), telephone access at home, and living in Kashan. Exclusion criteria: The the exclusion criteria are unwillingness to participate in the study and death

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Supportive care needs. Timepoint: Baseline, 2 weeks after the intervention, one month after intervention. Method of measurement: Supportive care needs survey short form 34(SCNS-SF34).

Secondary

MeasureTime frame
Psychological needs. Timepoint: baseline, two weeks and one month after intervention. Method of measurement: Psychological dimension of SCNS-SF34.;Health system & information needs. Timepoint: baseline, two weeks and one month after intervention. Method of measurement: Health system & information dimension of SCNS-SF34.;Physical & daily living. Timepoint: Baseline, two weeks and one month after intervention. Method of measurement: Physical & daily living dimension of SCNS-SF34.;Patient care & support. Timepoint: Baseline, two weeks and one month after intervention. Method of measurement: Patient care & support dimension of SCNS-SF34.;Sexual needs. Timepoint: Baseline, two weeks and one month after intervention. Method of measurement: Sexual dimension of SCNS-SF34.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParisa Javadie

Arak Medical Sciences University

parisa.javadi.89@gmail.com+98 86 4317 3524

Outcome results

None listed

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