This research project examines whether there are differences in effects between application of ImRs preceeded by CR and ImRs as a stand-alone treatment technique on the so-called encapsulated beliefs, cognitive beliefs based on the aversive…
ID
Source
Brief title
Condition
- Other condition
- Personality disorders and disturbances in behaviour
Synonym
Health condition
stemmingsstoornissen en angststoornissen
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
The difference between the encapsulated belief scores at pre-test, post-test
and one week follow up are the primary outcome measures. A scale ranging from 0
(not at all) to 100 (extremely) is used.
Secondary outcome
Change in vividness and distress of the aversive childhood memory addressed is
measured on a scale ranging 0 to 100.
To examine the reduction of overall symptomatology The Brief Symptom Inventory
(BSI) is included as a secondary parameter.
To check whether different emotional states are triggered throughout the study
the Modified Differential Emotions Scale (mDES) will be used.
During the one-week-follow-up the experience of CR and ImRs is investigated
with a qualitative interview.
Background summary
Previous research has shown treatment efficacy of imagery rescripting (ImRs)
for several disorders both as part of a treatment package and as a stand-alone
treatment. This technique, which is focused on imagining aversive memories and
changing its course fulfilling the needs of the individual, is used to change
the meaning or encapsulated belief and emotional valence people deduce from
childhood memories of adverse events. Additionally, ImRs is thought to alter
the vividness and distress of this memory. However, little is known regarding
necessity of specific ingredients for the ImRs to be efficient. For instance,
in some protocols within a treatment session ImRs is preceded by cognitive
restructuring (CR) whether other protocols only provide ImRs. CR is a common
therapeutic technique aimed at challenging maladaptive beliefs in a verbal way.
Some researchers have suggested that it is a necessary prerequisite for ImRs to
be successful as it prepares an adult perspective in phase 2 of ImRs (where the
adult intervenes in the averse childhood memory). However, others argue against
this by claiming that ImRs is powerful enough as a stand-alone technique and CR
is not needed to add to the ImRs procedure. The validity of CR as a preceding
element in the ImRs protocol has not been systematically studied yet.
Study objective
This research project examines whether there are differences in effects between
application of ImRs preceeded by CR and ImRs as a stand-alone treatment
technique on the so-called encapsulated beliefs, cognitive beliefs based on the
aversive childhood memory. Secondary aims focus on differences in effects
between aforementioned conditions with respect to the memory vividness and
distress of the aversive childhood memory addressed, overall symptomatology,
anxiety and depression symptoms, concepts related to positive psychology such
as self-compassion, patient experiences of the techniques and differences of
which emotional states are triggered and with what intensity.
Study design
This study is a randomized placebo-controlled clinical trial with a single
session intervention and a one-week follow-up session.
Intervention
This research project will employ the following conditions focused on the
application of ImRs on an aversive childhood memory 1) CR preceding ImRs, 2)
therapist attention placebo and ImRs 3) double therapist attention placebo. The
therapist attention placebos are common treatment elements not to be effective
to treat the complaints, but will be used as a placebo for therapist attention
of CR and ImRs.
Study burden and risks
There are no direct risks involved in the interventions. Every participant will
receive or already receives their regular treatment, thus none of the
participants will be without adequate treatment for their condition.
Participants can get emotional during retrieval of the aversive memories. The
benefit is some reduction of symptoms. Assessment 1 takes approximately 2,5
hours, including a 10-minute break. Assessment 2 has a duration of max. 45 min.
Universiteitssingel 40
Maastricht 6229ER
NL
Universiteitssingel 40
Maastricht 6229ER
NL
Listed location countries
Age
Inclusion criteria
- Meet the diagnostic criteria of a one or more diagnoses according to the DSM IV either/and on axis I (clinical disorders) and II (personality disorders)
- Free of medication or at least 2 months of stably set medication and maintaining the same dosage during participation of this study
- Age between 18 and 65 years
- IQ above 80
- Able to read and write in Dutch
Exclusion criteria
- Meet the diagnostic criteria of posttraumatic stress disorder an autism spectrum disorder or psychotic disorder accordingaccording to the DSM IV
- Suicidality or other self-damaging behaviour or damaging behaviour towards others
- Habitual use of benzodiazepines. In case of incidental use of benzodiazepines or betablockers participants are asked to refrain from this medication at the testing day. Participants using SSRI*s, TCA*s, or antipsychotic medication are asked to keep their medication stable till after the one week follow-up.
- Treatment experience with CBT
- Treatment experience with ImRs
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
CCMO | NL56227.068.15 |