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Parental Attitudes to Neoanus Dilatations Post-reconstruction in Anorectal Malformations

Parental Attitudes to Neoanus Dilatations Post-reconstruction in Anorectal Malformations

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05749406
Acronym
PANDA
Enrollment
20
Registered
2023-03-01
Start date
2023-07-01
Completion date
2024-07-01
Last updated
2023-05-25

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

Conditions

Anorectal Malformations

Brief summary

The goal of this qualitative clinical trial is to learn about parental attitudes and experiences of performing post-operative dilatation anal dilatations for their child with an anorectal malformation. The main question it aims to answer are: 1\. What are parental experiences/attitudes towards performing anal dilatations post-operatively. In the first part of the study, participants will take part in a small virtual focus group discussion to identify themes to aid design of a semi-structured interview for part 2. In part 2, participants will undergo a virtual semi-structured interview. The answers will be recorded, anonymised, transcribed and undergo thematic analysis.

Detailed description

Babies born without an anal opening require reconstructive surgery to create one, allowing them to pass stools. After the procedure, some surgeons recommend that parents perform routine dilatation of the anal opening using a metal rod dilator called a Hegar dilator. Recent studies have shown no difference in clinical outcomes for patients who have routine anal dilatation and those who do not. This study will look to find out the parental experiences and attitudes towards performing anal dilatation for their child. The study will be formed of 2 parts. Participants will all be parents who were asked to perform routine anal dilatation post-operatively for their child born with an anorectal malformation. In part 1, a focus group will be conducted via Microsoft teams to ascertain themes to formulate the questions for part 2. In part 2, individual semi-structured interviews will be performed via MS teams. The interviews will be recorded, anonymised, transcribed and undergo analysis to assess for common themes. The results will be published to guide professionals with regards to best practice and help inform parental discussions for new patients.

Interventions

OTHERFocus group

Small virtual focus group discussion about experiences/attitudes towards post-operative anal dilatation.

OTHERSemi-structured interview

Individual virtual interview to ascertain participant's experiences of performing anal dilatation post-operatively for their child with an anorectal malformation.

Sponsors

Verity Haffenden
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
16 Years to 100 Years
Healthy volunteers
Yes

Inclusion criteria

The parent of any patient who has: * Undergone a posterior sagittal anorectoplasty for anorectal malformation and been recommended post-operative anal dilatations * AND operation performed prior to November 2020 * AND able to understand and communicate in English * AND with access to a mobile/computer with MS Teams

Exclusion criteria

The parent of any patient who had has: * NOT undergone a posterior sagittal anorectoplasty for anorectal malformation * AND/OR, NOT been recommended post-operative anal dilatations * OR operated on after to November 2020 * OR unable to understand and communicate in English * OR without access to a mobile/computer with access to MS Teams

Design outcomes

Primary

MeasureTime frameDescription
Parental reported experience of anal dilatation3 monthsParental reported experience of anal dilatation; This is a qualitative study that will use thematic analysis to identify parental reported experiences of performing anal dilatations in children. No scale/questionnaire will be used to allow for appropriate breadth of response.

Contacts

Primary ContactVerity E Haffenden, MSc MBBS MRCS
verity.haffenden@gstt.nhs.uk07920745903

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026