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Do cancer patients experience less psychological distress with a brief psychological intervention package compared to routine clinical care?: A randomized controlled trial in a selected hospital in Sri Lanka

Do cancer patients experience less psychological distress with a brief psychological intervention package? : A randomized controlled trial in a selected hospital in Sri Lanka.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
SLCTR
Registry ID
SLCTR/2021/028
Enrollment
Unknown
Registered
2021-10-14
Start date
2021-10-30
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Psychological distress in cancer patients

Interventions

Study setting : A room adjoining the surgical clinic CSTH . Randomization method: The allocation ratio into two arms would be 1:1. Computer-generated random numbers will be used in randomization. Inte

Sponsors

Faculty of Medical Sciences, USJ
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients with new/ recent histopathological diagnosis /radiological diagnosis of a malignant lesion of any site 2. Age between 18-65 years 3. Both male and female patients 4.Cancer stage which is eligible for surgery as determined by investigation procedures and clinical judgment 5. Patients who are having HADS score more than > 6 will be recruited to the study

Exclusion criteria

Exclusion criteria: 1. Patients with already diagnosed psychiatric disorders (with a diagnosis of any one or more conditions specified under F00-F99 under ICD diagnosis research version (‘The ICD-10’, no date). 2. Patients with severe physical suffering and who are unwell to communicate or travel. 3. Patients who are diagnosed/carrying a card or past records with a severe learning disability, organic brain dysfunction due to cerebral deposits, diagnosed patients with dementia will not be recruited to the study) the research assistants will be trained for this using ICD diagnostic criteria for the research version. 4. Patients who are participating in other interventional studies. 5. Patients who are coming more than one week after breaking bad news. 6. Patients who are having HADS SCORE less than 6

Design outcomes

Primary

MeasureTime frame
Difference in HADS scores . [Before the intervention and 2 weeks after completing the intervention.. ]

Secondary

MeasureTime frame
Perceptions about - care package received from the hospital by the patient - general well-being - support patients received by the family using an in-house developed questionnaire [2 weeks after completing the intervention.. ]

Countries

Sri Lanka

Contacts

Public ContactPrasangika Senaviratne Alles

Consultant psychiatrist

dayanip@gmail.com0112802497

Outcome results

None listed

Source: SLCTR (via WHO ICTRP) · Data processed: Aug 9, 2026