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Training positive expectations for health: verbal suggestions versus imagery

Training positive expectations for health: verbal suggestions versus imagery - Training positive expectations for health

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON37467
Enrollment
126
Registered
2012-07-13
Start date
2012-12-01
Completion date
Unknown
Last updated
2025-03-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Op dit moment wordt het onderzoek bij gezonde proefpersonen uitgevoerd. In de toekomst zullen de interventies mogelijk toegepast kunnen worden bij de behandeling van een breed scala aan lichamelijke symptomen, waaronder pijn, jeuk en lichamelijke vermoeidheid not applicable

Interventions

Expectation effects are induced by means of (1) positive versus neutral verbal suggestions (that it is effective for 95% versus 5% of people) of the effectiveness of a substance that is, unknown to

Sponsors

Universitair Medisch Centrum Sint Radboud
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Age >= 18 years fluent in Dutch language

Exclusion criteria

Exclusion criteria: 1) Severe physical or psychological morbidity (e.g., heart and lung diseases, or DSM-IV psychiatric disorders) that would adversely affect participation 2) Chronic pain, itch, or fatigue complaints at present or in the past 3) Use of beta-blockers or other medication that influence heart rate, use of pacemaker 4) Inadequate health for physical exercise as indicated by 1 or more positive responses on the PAR-Q (Physical Activity Readiness Questionnaire) 5) Participants are required not to consume coffee, tea or cola within a 2 hour period prior to the experiment. Nor should they have smoked in the last two hours or consumed alcohol or other drugs in the last 24 hours. Additionally they are required to refrain from heavy physical exercise 24 hours prior to the experimental session

Design outcomes

Primary

MeasureTime frame
The primary endpoint of this study is the effectiveness of the expectation manipulations in affecting sensitivity to pain, itch, and fatigue, i.e. the difference between the conditions in sensitivity to pain, itch, and fatigue after the expectation manipulations, as rated on Visual Analogue Scales (VAS).

Secondary

MeasureTime frame
The secondary endpoints of this study are to explore the effects of the expectation manipulations on autonomic (heart rate, alpha amylase) and endocrine responses (cortisol), as well as to explore the influence of individual characteristics (e.g., general expectations) on the effectiveness of the expectation manipulations.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)