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- Klinische proef NCT02493127
The Effect of Priming of Questionnaire Content on Grip Strength in Patients With Hand and Upper Extremity Illness
Objectives:
To determine the association between priming and measurements of hand function such as grip strength
Primary null hypothesis:
There is no difference in grip strength (best of three attempts) as a percent of the opposite hand between patients that complete the standard Pain Catastrophizing Scale (PCS) compared to patients that complete the positively adjusted PCS.
Secondary null hypotheses:
There is no difference in grip strength (last of three attempts) as a percent of the opposite hand between patients that complete the standard PCS compared to patients that complete the positively adjusted PCS.
There is no difference in grip strength (best of three attempts) before and after completing the questionnaires between patients that complete the standard PCS compared to patients that complete the positively adjusted PCS.
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
Studietype
Inschrijving (Werkelijk)
Fase
- Niet toepasbaar
Contacten en locaties
Studie Locaties
-
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Massachusetts
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Boston, Massachusetts, Verenigde Staten, 02114
- Massachusetts General Hospital
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-
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
Inclusion Criteria:
- All English-speaking adult patients visiting the Orthopaedic Hand and Upper Extremity Service
Exclusion Criteria:
- Unable to complete enrollment forms due to mental status or language problem
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Dubbele
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
---|---|
Experimenteel: Standard PCS
Grip strength measurements and completes standard PCS
|
Subject completes the standard version of the PCS Questionnaire
Research Assistant takes Grip Strength Measurements
|
Experimenteel: Positive PCS
Grip strength measurements and completes positively adjusted PCS
|
Research Assistant takes Grip Strength Measurements
Subject completes the positively-adjusted version of the PCS Questionnaire
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
---|---|---|
Pain Catastrophizing Scale (PCS)
Tijdsspanne: enrollment
|
The pain catastrophizing scale is a 13-item scale to measure catastrophic thinking.
The scale is from 0-4 and scores range from 0-52, a lower score indicates less catastrophic thinking about pain.
|
enrollment
|
Positive Pain Catastrophizing Scale (PCS)
Tijdsspanne: enrollment
|
The positive pain catastrophizing scale (PCS) is a positively-phrased 13-item scale to measure catastrophic thinking.
The scale is from 0-4 and scores range from 0-52, a higher score indicates less catastrophic thinking about pain.
|
enrollment
|
Difference in Grip Strength Measured With Dynamometer
Tijdsspanne: Day 1
|
Difference in Grip strength of the non-affected hand after completing intervention.
Each participant completed the grip strength measurement 3 times on the non-affected hand at enrollment (day 1).
The results reported represent an increase or decrease in mean grip strength and maximum grip strength after completing the intervention.
|
Day 1
|
Difference in Grip Strength Measured With Dynamometer
Tijdsspanne: Day 1
|
Difference in Grip strength of the injured hand after completing intervention.
Each participant completed the grip strength measurement 3 times on the injured hand at enrollment (day 1).
The results reported represent an increase or decrease in mean grip strength and maximum grip strength after completing the intervention.
|
Day 1
|
Difference in Grip Strength Measured With Dynamometer
Tijdsspanne: Day 1
|
Difference in Grip strength of both hands after completing intervention.
Each participant completed the grip strength measurement 3 times with both hands at enrollment (day 1).
The results reported represent an increase or decrease in mean grip strength and maximum grip strength after completing the intervention.
|
Day 1
|
Medewerkers en onderzoekers
Sponsor
Studie record data
Bestudeer belangrijke data
Studie start
Primaire voltooiing (Werkelijk)
Studie voltooiing (Werkelijk)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Schatting)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Andere studie-ID-nummers
- 2015P000879
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-
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-
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-
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-
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-
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-
National Taiwan University HospitalOnbekend
-
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