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Brief online writing exercise to support individuals living with a stoma

Effect of expressive writing intervention on body image and quality of life in individuals with a stoma

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12619000087156
Acronym
N/A
Enrollment
140
Registered
2019-01-22
Start date
2019-05-09
Completion date
2019-06-29
Last updated
2019-09-30

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

Conditions

None listed

Brief summary

The primary purpose of this study is to investigate the effects a brief, one-off writing exercise can have on the psychological outcomes of individuals living with a stoma. The study design is a mixed analysis of variances (MANOVA) comparing 2 groups (intervention and control condition) across 3 time points (baseline, one week and one month following the writing exercise). It is hypothesised that those in the intervention condition will see statistically significant improvements in a range of psychological outcomes, and more so in comparison to those in the control condition.

Interventions

This study is a brief, online expressive writing exercise (based on Pannebaker's expressive writing paradigm) accompanied by one online baseline and two follow-up questionnaires. This study is replicating a study that used self-compassion expressive writing to help reduce body-image distress in breast cancer survivors (Sherman et al., 2018). Before deciding to take part in the study, participants must read the Participant Information Sheet (PIS) and Consent Form. These will be available on our s

This study is a brief, online expressive writing exercise (based on Pannebaker's expressive writing paradigm) accompanied by one online baseline and two follow-up questionnaires. This study is replicating a study that used self-compassion expressive writing to help reduce body-image distress in breast cancer survivors (Sherman et al., 2018). Before deciding to take part in the study, participants must read the Participant Information Sheet (PIS) and Consent Form. These will be available on our study web page (yet to be designed). After consenting to the study, participants will complete an online baseline questionnaire that will take approx. 15 minutes to complete (though there is no time restriction). It will include demographic information and medical history related to their stoma, followed by questions on various psychological measures (body image, self-compassion, quality of life, depression/ anxiety/ stress, and disgust propensity and sensitivity. The questionnaire (and following writing exercise and follow-up questionnaires can be completed at a device/ computer of the participant's choice). Participants (via REDCap software) will then be randomly allocated to either the intervention writing exercise (condition 1) or the control writing exercise (condition 2) and automatically sent a link to the appropriate exercise. Those in condition 1 will complete the online writing exercise by following six guided self-compassion prompts and write about a negative experience or event they have experienced (i.e. having their stoma constructed). he wording was modified slightly to be relevant to stoma patients (i.e. 'from 'Think about how your body has changed through the experience with a breast cancer diagnosis and treatment' to 'Think about how your body has changed through your experience with having your stoma constructed'). Those in condition 2 will also have prompts to write about a negative event, but these will be generic (i.e. 'Please describe the event further'). Both writing exercises will take up to 30 minutes to complete (depending on participants' typing speed, time spent considering what to write). There is no restriction/ limit on how many words/ characters participants must write. Participants will then be sent follow-up questionnaires (a shortened version of the baseline questionnaire; should take 10 mins max.) one week and one month following the writing exercise. These will also be completed online. The Disgust Propensity and Sensitivity Scale items will not be included in the follow-up questionnaires.

Sponsors

Dr. Lisa Reynolds
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Educational / counselling / training
Masking
Blinded (masking used) (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

- 18+ years - Fluent in English (reading and writing) - Stoma for at least the duration of the study - Live in New Zealand or Australia

Exclusion criteria

- Younger than 18 years of age - Cannot fluently write and read in English - Stoma for less than the duration of the study

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026