This project aims to investigate the additive value of an optimism intervention to an existing rehabilitation protocol for pain patients. It is expected that including an optimism module in an exposure in vivo treatment or a graded activity…
ID
Source
Brief title
Condition
- Other condition
Synonym
Health condition
chronische pijn
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
Primary outcome of the study will be the performance of personally relevant
activities (versus disability).
The performance of personally relevant activities is measured by means of daily
diary items that are based on information that was gathered during the
screening of participants. Functioning (versus disability) will also be
measured by means of a daily dairy item.
Although the analyses primarily use daily dairy items, all basic constructs in
this study are also measured by means of questionnaires. More specifically, the
pain disability index (PDI) is measured to assess functioning/disability.
Secondary outcome
The following secundary outcomes are measured:
- Fear of movement/(re)injury: 4 daily diary items borrowed and adjusted from
the Tampa Scale of Kinesiophobia (TSK)
- Pain related catastrophizing: 3 daily diary items borrowed and adjusted from
the Pain Catastrophizing Scale (PCS)
- Pain intensity(/unpleasantness): 2 selfconstructed dialy diary items
- Subjective well-being: 1 self-constructed daily diary item and the
Satisfaction with LIfe Scale (SWLS)
- Psychological distress: 1 self-constructed dialy diary item and the Hospital
Anxiety and Depression Scale (HADS)
- Positive (and negative affect): 2 self-constructed daily diary items and the
Positive and Negative affect Schedule questionnaire (PANAS)
- Optimism: 1 self-constructed daily dairy item and the Life Orientation Test
Revised (LOTR)
Data regarding psychological flexiblity (PIPS), fear (PHODA), personal relevant
activities (COPM) and pain self-effectivity (PSEQ) is automatically collected
at certain moments during the exposure treatment at Adalante. This data will be
analysed in an explorative manner.
Background summary
Chronic pain is a major health problem, leading to various limitations in daily
life. According to the Fear-Avoidance model of pain, learned fear of painful
movements and avoidance behaviour instigate pain disability. Exposure
treatments aim to correct dysfunctional beliefs patients may have about
activities and movements to promote functional recovery. Although exposure
treatments have proven successful, we know from anxiety research that a subset
of patients may fail to achieve satisfactory results at the end of the exposure
treatment or may experience relapse following successful exposure. Inhibitory
learning, exposure treatment's key process in which a new safety-based
association about a feared movement (e.g. playing tennis - no harm) is learned
so that it can compete with the previously learned fear-based association (e.g.
playing tennis - injury) might be diminished and cause poor exposure effects.
Enhancing inhibitory learning in an exposure treatment might lead to enhanced
clinical effects in patients receiving exposure in vivo.
Positivity may support inhibitory learning. We know that several memory
processes and prerequisites for learning (e.g. motivation and attention) are
influenced by positivity. Support for this notion also arises from experimental
research in which inducing positive expectations has been linked to enhanced
fear extinction and diminished fear retrieval. Clinically relevant evidence for
the bolstering effect of optimism on inhibitory learning is however still
lacking.
Study objective
This project aims to investigate the additive value of an optimism intervention
to an existing rehabilitation protocol for pain patients. It is expected that
including an optimism module in an exposure in vivo treatment or a graded
activity treatment with exposure elements leads to stronger increases in the
performance of personally relevant goals (versus disability) and stronger
decreases in fear of movement, pain catastrophizing, pain an distress (versus
well-being).
This study might provide a first clinical indication of the effect of inducing
positivity in the rehabilitation of chronic pain patients. The study may
contribute to optimizing rehabilitation treatment for chronic pain patients.
Study design
A series of replicated randomised two-phase (AB) single-case experiments will
be used. Specialized rehabilitation treatment (A-phase) will be compared to
optimism enriched specialised rehabilitation treatment (B-phase) within 8
participants. The start of the two-week optimism module will be randomized
between participants. The optimism module is based on earlier successful work
with the Best Possible Self exercise, a writing and visualisation exercise
focused on positive future expectations.
Intervention
A positive psychology module aimed at inducing optimism will be used in this
study. This optimism module uses the Best Possible Self (= BPS) exercise, a
writing and visualisation exercise focused on one*s best possible self in the
future. The BPS has repeatedly and successfully been used as a single
exercise/module or as a module in a multi-modular positive psychology
intervention in chronic pain patients. The duration of the optimism module is 2
weeks. The module is designed as an online program that participants can work
on independently. Assistance is provided by means of telephone contact (1 fixed
appointment of 20-30 minutes) and e-mail correspondence with one of the
research team members. This module is introduced at a random moment during the
treatment that participants receive at the rehabilitation center of Adelante
Maastricht.
Study burden and risks
Burden is mainly related to the time invested that is asked of the participants.
The following time consuming activities are being asked of all participants:
- filling in a survey (15-20 minutes) at 5 times
- filling in a short daily diary (few minutes) 2 weeks prior, during and 2
weeks post exposure treatment.
In addition, the participants will spend +-3.5 hours on the online optimism
module and +-30 minutes on a scheduled telephone call with the research team.
Universiteitssingel 40
Maastricht 6229ET
NL
Universiteitssingel 40
Maastricht 6229ET
NL
Listed location countries
Age
Inclusion criteria
Patients with chronic primary pain syndromes who are indicated for and willing
to engage in an exposure treatment or graded activity treatment (with exposure
elements) as specialized care and who have good knowledge (reading/writing) of
the Dutch language.
Exclusion criteria
> 65 years old, psychopathology/situation that interferes with exposure /
graded activity treatment, no good knowledge of the Dutch language, no internet
access, pregnancy
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 | NL79951.096.21 |