The Hold me Tight Program for Couples Facing Huntington's Disease

Tara M Petzke1,2, Mar Rodriguez-Girondo3, Lucienne B van der Meer1

  • 1Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.

Insights

The Hold Me Tight program improved wellbeing and relationship satisfaction for couples with Huntington's disease (HD). This emotionally focused therapy strengthens relationships, offering support for genetic neurological disorders.

Area of Science:

  • Psychology
  • Genetics
  • Therapeutic Interventions

Background:

  • Genetic testing for Huntington's disease (HD) significantly impacts couples' wellbeing and relationship stability.
  • The Hold Me Tight (HmT) program, rooted in emotionally focused therapy, aims to bolster couple bonds by addressing attachment needs.

Purpose of the Study:

  • To evaluate the effectiveness of the adapted HmT program in strengthening relationships for couples where one partner is a presymptomatic HD carrier.
  • To assess the program's impact on relationship satisfaction, wellbeing, and resilience.

Main Methods:

  • A multiple baseline design study involving 15 couples with presymptomatic HD carriers.
  • Couples participated in an 8-session adapted HmT program over 19 weeks, completing weekly self-report questionnaires.
  • Attachment style, resilience, relationship satisfaction, and wellbeing were measured, with data analyzed using a multi-level model.

Main Results:

  • Significant improvements were observed in participants' wellbeing and relationship satisfaction.
  • Resilience did not show a significant change over the study period.
  • Attachment style moderated outcomes, with more securely attached individuals experiencing better results.

Conclusions:

  • The adapted HmT program effectively enhanced wellbeing and relationship satisfaction for couples affected by Huntington's disease.
  • High acceptability suggests HmT could be integrated into standard HD care.
  • The program's adaptability makes it suitable for couples facing other genetic neurological disorders.
Abstract

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