Status:

COMPLETED

Online Mindfulness-based Cognitive Therapy for Parents of Children With Food Allergies

Lead Sponsor:

Canterbury Christ Church University

Collaborating Sponsors:

University of Surrey

Conditions:

The Quality of Life of Parents of Children With Food Allergy

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

This study aims to conduct an initial evaluation of adapted, live online, mindfulness-based cognitive therapy for parents and carers of children with food allergies (MBCT-PCCFA).

Detailed Description

This study is a pilot randomised controlled trial (RCT) comparing adapted, live online, mindfulness-based cognitive therapy for parents and carers of children with food allergies (MBCT-PCCFA) with a t...

Eligibility Criteria

Inclusion

  • Parents or caregivers who identify as having a child under the age of 18 with a food allergy
  • The allergy has been diagnosed by a qualified physician (e.g. GP or allergy specialist)
  • Mean score of \>=2 on the FAQL-PB, indicating they are at least 'somewhat limited/troubled' by their child's allergy (Cohen et al., 2004).
  • Resident in the United Kingdom
  • Have access to email, a PC/laptop/tablet with a webcam and microphone and internet access to allow videoconferencing

Exclusion

  • They had consulted on the design and content of the intervention or study
  • They have already participated in a substantial mindfulness-based course
  • They are currently engaged or are planning to engage with another psychological intervention during the course of the study
  • They currently engage in regular mindfulness-based practice
  • They do not have the practical means and time available to be able to attend the intervention during the dates outlined on the information sheet and commit to at-home practice
  • They have scores \>19 on PHQ-8 (indicating 'severe' depressive symptom severity; Kroenke et al., 2009) or \>15 on GAD (indicating 'severe' level of anxiety; Spitzer et al., 2006)
  • They have a problem with alcohol or recreational drug misuse
  • They have experienced thoughts about harming themselves or others in the last 12 months
  • They have been given a diagnosis of psychosis
  • They are currently experiencing high levels of distress and/or currently feeling particularly fragile
  • They have experienced a bereavement of someone close to them in the last year or are continuing to experience continuing grief in relation to losing someone further back in time
  • They have had traumatic experiences that they continue to be troubled by (including, but not limited to, receiving diagnosis of post-traumatic stress disorder)
  • They experience significant difficulty being in a group with other people.
  • NB: for further details re the FAQL-PB and PHQ-8, please see the outcome measures section.

Key Trial Info

Start Date :

March 2 2021

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

February 2 2022

Estimated Enrollment :

46 Patients enrolled

Trial Details

Trial ID

NCT04738890

Start Date

March 2 2021

End Date

February 2 2022

Last Update

December 17 2024

Active Locations (1)

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Salomons Institute for Applied Psychology

Royal Tunbridge Wells, Kent, United Kingdom, TN1 2YG