Health Services Evaluation Pilot: Promoting an improved patient experience in gynaecological cancer care through supportive care screening and intervention.

Not Applicable

Recruiting

• Conditions: Gynaecological cancer; Mental health; Cancer - Ovarian and primary peritoneal; Cancer - Cervical (cervix); Mental Health - Studies of normal psychology, cognitive function and behaviour

• Registration Number: ACTRN12615000428561
• Lead Sponsor: niversity of Melbourne

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2015-05-06
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 130

Inclusion Criteria

1.New diagnosis of any gynaecological cancer
2.Undergoing treatment at the Royal Women’s Hospital
3.Age greater than or equal to 18 years old

Exclusion Criteria

1.Age less than 18 years old
2.Language other than English

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Patient experience score[3-6 months post initial treatment (either surgery or chemotherapy)];SF-12 score - to assess patients' quality of life[3-6 months post initial treatment (either surgery or chemotherapy)];CHIERS Eco-mapping score (intervention group)[At the time of the delivery of the intervention i.e. at the commencement of treatment. This could be days-weeks post randomisation, depending on when surgery or chemotherapy is planned. ]

Secondary Outcome Measures

Name	Time	Method
Treatment completion data - to assess whether patient's follow their intended treatment trajectory (i.e. do they complete surgery and chemotherapy if that is what was planned)[3-6 months post initial recruitment]