Parental Attitudes to Neoanus Dilatations Post-reconstruction in Anorectal Malformations

NCT ID: NCT05749406

Last Updated: 2023-05-25

Basic Information

• Recruitment Status: UNKNOWN
• Total Enrollment: 20 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2023-07-01
• Study Completion Date: 2024-07-01

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.

Conditions

Anorectal Malformations

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: RETROSPECTIVE

Interventions

Focus group

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

Intervention Type: OTHER

Semi-structured interview

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

Intervention Type: OTHER

Eligibility Criteria

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

• Minimum Eligible Age: 16 Years
• Maximum Eligible Age: 100 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Verity Haffenden

OTHER

Sponsor Role: lead

Responsible Party

Verity Haffenden

Clinical Research Fellow in Paediatric Surgery

Responsibility Role: SPONSOR_INVESTIGATOR

Central Contacts

Verity E Haffenden, MSc MBBS MRCS

Role: CONTACT

verity.haffenden@gstt.nhs.uk

07920745903

Other Identifiers

313255

Identifier Type: -

Identifier Source: org_study_id