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A randomised controlled trial assessing effectiveness of six sessions of brief cognitive behaviour therapy in reducing psychological distress in women who have completed a course of intravenous chemotherapy for ovarian cancer

A randomised controlled trial assessing effectiveness of six sessions of brief cognitive behaviour therapy in reducing psychological distress in women who have completed a course of intravenous chemotherapy for ovarian cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN60459823
Enrollment
Unknown
Registered
2003-09-12
Start date
2002-04-26
Completion date
Unknown
Last updated
2018-02-26

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

Conditions

Ovarian cancer Cancer Malignant neoplasm of ovary

Interventions

Current information as of 11/08/2009: At the end of chemotherapy those who have consented to the study will be asked to complete a Hospital Anxiety and Depression Scale (HADS) to assess their suitabi

Sponsors

Department of Health (UK)
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Current information as of 11/08/2009: 1. Patients newly diagnosed with ovarian cancer, attending the outpatient clinic of Dr G Jayson 2. Age <55 years 3. Written informed consent 4. Hospital Anxiety and Depression Scale (HADS) score of 7 Initial information at time of registration: Patients with ovarian cancer, who are less than 55 years of age, will be giving an information sheet outlining the study.

Exclusion criteria

Exclusion criteria: Does not match inclusion criteria

Design outcomes

Primary

MeasureTime frame
Added 11/08/2009: Women in both arms of the study will be assessed using: 1. HADS and Worry About Cancer Scale 2. A Social Support Inventory (SSI) 3. an Impact of Events Scale 4. A scale assessing the beliefs about controllability and social worry These will be administered at the end of chemotherapy and 3 months following completion of chemotherapy. These questionnaires will be administered by a member of the research team who will not be involved in the cognitive behaviour therapy sessions.

Secondary

MeasureTime frame
Not provided at time of registration

Countries

United Kingdom

Outcome results

None listed

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