NCT02260999

Completed

Experimental Study of Detection an Intentional Performance D...

Christoph Maier, Prof. Dr.Source

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Other study identifiers

Sponsor study identifier

BHL-2113

Study Type

observational

Actual enrollment (reported)

136

Locations

0 countries

Sites

N/A

Timeline

Study Start

May 2012

Date type not reported

This date has not been verified as actual or estimated.

Primary Completion

February 2014

Actual (reported)

Study Completion

March 2014

Actual (reported)

Brief Summary

In this study, the detection of the feigning weakness in grip strength is measured using different grip strength testing instruments. Patients with injury of the upper limb are compared to patients with injury of the lower limb as well as healthy controls.

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: completed
Actual enrollment (reported): 136 participants
Study completion date: March 2014
Actual (reported)
Listed locations: 0 countries · 0 sites

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

Study Start
May 2012
Date type not reported
This date has not been verified as actual or estimated.
Primary Completion
February 2014
Actual (reported)
Study Completion
March 2014
Actual (reported)
First Submitted
October 6, 2014
Actual (reported)
First Posted
October 9, 2014
Actual (reported)

Last Updated: October 9, 2014
Status Verified: October 2014
Last Update Submitted: October 6, 2014

Conditions

Pain

Outcome Measures

Primary Outcomes (2)

grip strength
mean and maximum grip strength measured by rapid exchange grip and isometric grip strength testing
1 hour
range of motion
measured by the handtutor
1 hour

Study Arms (3)

healthy

\> 18 years old sufficient language knowledge

chronic pain patients

patients with injury at the upper etxremity

Eligibility Criteria

Age18 Years - 90 Years

Sexall

Healthy VolunteersYes

Age GroupsAdult (18-64), Older Adult (65+)

Sampling MethodProbability Sample

Study Population

chronic pain patients patients with injury at the upper extremity healthy subjects

You may qualify if:

\- \>18 years, signed consent form, stable pain mediaction for 48 hours

You may not qualify if:

Sponsors & Collaborators

Christoph Maier, Prof. Dr.
Otherlead

MeSH Terms

Conditions

Pain

Condition Hierarchy (Ancestors)

Neurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Enrollment

136 participants (actual enrollment reported by the registry).

Study Design

Study Type: observational
Observational Model: CASE CONTROL
Time Perspective: PROSPECTIVE
Sponsor Type: OTHER
Responsible Party: SPONSOR INVESTIGATOR
PI Title: Prof. Dr.med. C. Maier

Study Record Dates

First Submitted

October 6, 2014

First Posted

October 9, 2014

Study Start

May 2012

Date type not reported

This date has not been verified as actual or estimated.

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Phase 4Completed

\- \<18, unsigned consent form, dose change of the pain medication during the last 48 hours...

Contact the study team to confirm eligibility.

Primary Completion

February 2014

Actual (reported)

Study Completion

March 2014

Actual (reported)

Last Updated

October 9, 2014

Record last verified: 2014-10

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

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Registry identifier: NCT02260999
Data provider: ClinicalTrials.gov
Source updated: 2014-10-09
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:25:34 UTC

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

Primary Completion

Study Completion

First Submitted

First Posted

Conditions

Outcome Measures

Primary Outcomes (2)

Study Arms (3)

healthy

chronic pain patients

patients with injury at the upper etxremity

Eligibility Criteria

You may qualify if:

You may not qualify if:

Sponsors & Collaborators

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Enrollment

Study Design

Study Record Dates

Source record