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The effect of a multi-professional support program on the burden of symptoms and the activity of the elderly with gastrointestinal cancer

The effect of a multi-professional support program on the burden of symptoms and the activity of the elderly with gastrointestinal cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240723062519N1
Enrollment
88
Registered
2024-08-14
Start date
2024-09-22
Completion date
Unknown
Last updated
2024-08-26

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

Conditions

Condition 1: Gastrointestinal cancer. Condition 2: Multi-professional support program. Condition 3: Symptom burden. Condition 4: Elder. Malignant neoplasm of ill-defined sites within the digestive system

Interventions

Intervention 1: Intervention: In the first face-to-face meeting with the patient, the patient will complete the questionnaires of personal characteristics, Edmonton symptom burden and patient activati

Sponsors

Research assistant of Lorestan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: Definite diagnosis of gastrointestinal cancer, including esophageal cancer, stomach cancer, colon cancer, colorectal cancer, with inclusion in the medical record by a specialist Elderly and over 60 years old Ability to verbally communicate in Persian or an understandable local dialect Full consent to participate in research work The expected cycle of chemotherapy with an interval of 2 weeks (sometimes based on the opinion of the doctor and the clinical condition of the patient and the type of drug regimen in gastric cancer chemotherapy is three weeks, which is not used in the study) The patient's awareness of having cancer and undergoing chemotherapy Passing at least two sessions of chemotherapy (due to lack of resistance and participation in research activities and the onset of symptoms and side effects of chemotherapy)

Exclusion criteria

Exclusion criteria: Not suffering from a mental or cognitive disorder such as Alzheimer's.. to cooperate in the study

Design outcomes

Primary

MeasureTime frame
Load of symptoms. Timepoint: 2 months, a week before, a month after. Method of measurement: The score obtained from the Edmonton Symptom Assessment Scale.;Activation. Timepoint: 2 months, a week before, a month after. Method of measurement: The score obtained from the patient activation measurement questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactReza Hossein Abadi

Khoram-Abad University of Medical Sciences

Reza_hosseinabadi@yahoo.com+98 66 3312 0174

Outcome results

None listed

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