Clinical trial · Interventional
The Impact of Mindful Compassion on Sexual Functioning and Quality of Life in Home Hospice Care
The Impact of Mindful Compassion on Supporting Women Post-cancer Treatment's Sexual Functioning and Quality of Life in Home Hospice Care: A Preliminary Randomised Controlled Trial.
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Sexual dysfunction is commonly reported post cancer treatments. Indeed, sexual wellbeing can be affected by diagnosis, medication and cancer treatments, which can damage body tissues such as the vagina owing to radiation therapy, or insufficient lubrication caused by chemotherapy. Additionally, feeling sore, exhausted, anxious, depressed and 'not in the mood' further contribute to changes in sexual desire Very few evidence based online interventions have been developed to address sexual difficulties post cancer treatments and in hospice at home care. This extends to well being and quality of life. Mindful compassion interventions has been based on a behavioural taxonomy to support the reliability of their delivery. Indeed, this study aims to identify and describe the key components and behaviour change techniques as part of the online intervention. These have been mapped to a behaviour change taxonomy with the view of supporting standardisation for future trial implementation. Therefore, the aim of this study is to examine the effectiveness of an online mindful compassion intervention using the 3 system model of emotions among a post cancer treatment group in hospice care, at the end of life, to improve quality of life. The study intends to provide preliminary estimates of pre-post intervention on a waitlist controlled randomised controlled trial looking at well being, sexual function, mindfulness and self compassion. Quantitatively, the research is structured so that participants will be randomised to either the active experimental or delayed group. This intervention will be weekly for approximately 1 to 2 hours over 4 weeks. This A follow up at 12 weeks will be taken to determine the sustainability of this intervention. Feedback questions will also be given during the delivery of the intervention.
Conditions
Conditions (4)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| End of Life | — | UNRESOLVED | — |
| Quality of Life | — | UNRESOLVED | — |
| Sexual Function Disturbances | — | UNRESOLVED | — |
| Well-Being, Psychological | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Mindful compassion | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Active group
- description
- Mindful compassion group provided over 4 weeks
- interventionNames
- Behavioral: Mindful compassion
- type
- ACTIVE_COMPARATOR
- label
- Delayed group
- description
- Mindful compassion group commences at week 4 when the active group intervention terminates.
- interventionNames
- Behavioral: Mindful compassion
Primary outcomes (4)
- measure
- Female Sexual Function Index
- timeFrame
- 0, 4 and 12 weeks
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
- Maximum age
- 100 Years
Show eligibility criteria text
Inclusion Criteria: * Were in hospice care with a cancer diagnosis/terminal * We're receiving support and care * Identified as female * Registered with a healthcare service or charity * Self-perceived satisfactory sexual intimacy before cancer diagnosis (Acquired) * Aged 18 years or older * Had a computer, laptop, mobile phone- intervention was online. * Read and wrote English, as the intervention was delivered in English * Patient Health Questionnaire 9 screening (score range from minimal to moderate, 0-14). * Mental Capacity Mini Cog outcomes 3,4,5 (cognitive comprehension) Exclusion Criteria: * Were not in hospice care with a cancer diagnosis/terminal * Did not identify as female * Were very late-stage palliative/hospice care in which capacity (medication) may be compromised, or discomfort is experienced * Were aged below 18 years old * Had reading and writing difficulties in English * Had a moderate to severe to high Patient Health Questionnaire 9 screening score (ranging from moderate to severe 15-27). * Mental Capacity Mini Cog outcomes 0,1,2 (problematic cognitive comprehension)
References
Publications (10)
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