The Psychological Impact of GTN on Women Who Have Completed Chemotherapy Treatment

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age16-55
SponsorSheffield Teaching Hospitals NHS Foundation Trust

About this trial

A cross-sectional retrospective study of a sample of 20 women who completed single agent or multi agent chemotherapy: between 6 weeks and 24 months post treatment involving a semi structured telephone interview. A patient sample of 20 is proposed for the study. These are all the patients who meet the inclusion criteria below and are thus eligible for the study. These patients will be contacted via telephone by the principal investigator to inform them of the study and invite participation. A proposed sample size of 20 is sufficient to generate data to address the central questions and furthermore, this sample size is adequate because the intention is to gain insight into the experiences of patients' perceptions about their psychological experiences.

Objectives:

* Gaining insight into the emotional impact of GTN post treatment * Ascertaining if health professionals are providing adequate psychological support * Identifying sources of support that patients accessed post completion of treatment * Identifying potential areas of improvement in the follow up support for future patients

Criteria for inclusion:

* Treated with chemotherapy for a GTN diagnosis * Completed treatment between 6 weeks and 24 months * Are able to provide informed consent * Have no cognitive impairment as judged by the treating clinician

Criteria for exclusion

* Treatment received less than 6 weeks ago * Treatment received more than 24 months ago * Non-English speaking

Outcome measures are not appropriate in this qualitative study. However outputs from this study include increasing knowledge and insight into:

* patients' experiences of their psychological experiences post chemotherapy * patients' perspective of the support received after their treatment * potential areas of improvements in care

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Treated with chemotherapy for a GTN diagnosis

Completed treatment between 6 weeks and 24 months

Are able to provide informed consent

Have no cognitive impairment as judged by the treating clinician

Disqualifiers

Treatment received less than 6 weeks ago

Treatment received more than 24 months ago

Non-English speaking

Trial population

A patient sample of 20 is proposed for the study. These are all the patients who meet the inclusion criteria and are thus eligible for the study. The patients will have a history of Gestational Trophoblastic Neoplasia, and have received chemotherapy between 6 weeks and 24 months ago, and presented to Weston Park Cancer Centre for this treatment.

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

Not listed

Trial groups

20 Participants
are grouped into 1 trial group
Group A: Chemotherapy-treated GTN Patients

Trial outcomes

Primary outcomes

1

Common themes of psychological experiences post-chemotherapy

Thematic analysis will be used to interpret common themes of patient experiences following chemotherapy for GTN

Time frame
1 hour interviews
2

Common opinions of post-treatment support

Thematic analysis will be used to interpret common patient perspectives of the support received after their treatment

Time frame
1 hour interviews
3

Themes of Suggested Improvement in Patient Care

Thematic analysis will be used to interpret common suggestions of how patient care can be improved for those receiving chemotherapy for GTN.

Time frame
1 hour interviews

Secondary outcomes

Other outcomes

Sponsors and contacts

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