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The effect of occupational therapy in women with breast cancer

The effect of an online occupation-based intervention program on arm lymphedema, spirituality, occupational performance, sexuality function and adaptive response in women with breast cancer

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20211220053459N2
Enrollment
40
Registered
2023-03-07
Start date
2023-03-01
Completion date
Unknown
Last updated
2023-03-13

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: Participants in the intervention group will receive a combined program including lymphatic therapy (CDT) and an individual, remote (telephone and available applicat

Sponsors

Semnan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Ability to verbally communicate and speak in Persian Read and write Being over 18 years of age Having access to a telephone Get a score above 22 on the MMSE cognitive test Histologically confirmed malignancy based on the physician's diagnosis

Exclusion criteria

Exclusion criteria: People with brain metastases Mental disabilities Psychosis Dementia

Design outcomes

Primary

MeasureTime frame
Level of occupational performance and satisfaction of occupational performance. Timepoint: Before the intervention, after the intervention and one month after the intervention. Method of measurement: Canadian Occupational Performance Measurement.;Adaptation. Timepoint: Before the intervention, after the intervention and one month after the intervention. Method of measurement: Relative Mastery Scale.

Secondary

MeasureTime frame
Spirituality. Timepoint: En Before the intervention, after the intervention and one month after the intervention. Method of measurement: the 12-item Spiritual Well-being scale.;Lymphedema. Timepoint: Before the intervention, after the intervention and one month after the intervention. Method of measurement: The Persian version of the Lymphedema Life Impact Scale (LLIS).;Sexual Function. Timepoint: Before the intervention, after the intervention and one month after the intervention. Method of measurement: The Female Sexual Function Index (FSFI).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Motaharinezhad

Semnan University of Medical Sciences

fatemeh.motahari64@yahoo.com+98 23 3332 2035

Outcome results

None listed

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