NCT06834919

Brief Summary

To translate and validate the Upper Limb Functional Index into Albanian for use in the Albanian-speaking population.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
200

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Feb 2025

Shorter than P25 for all trials

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 13, 2025

Completed
5 days until next milestone

Study Start

First participant enrolled

February 18, 2025

Completed
1 day until next milestone

First Posted

Study publicly available on registry

February 19, 2025

Completed
9 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 28, 2025

Completed
15 days until next milestone

Study Completion

Last participant's last visit for all outcomes

March 15, 2025

Completed
Last Updated

February 19, 2025

Status Verified

February 1, 2025

Enrollment Period

10 days

First QC Date

February 13, 2025

Last Update Submit

February 13, 2025

Conditions

Upper Limb FunctionUpper Limb PainUpper Limb; Injury, Superficial, MultipleUpper Limb Rehabilitation

Outcome Measures

Primary Outcomes (1)

  • Upper Limb Functional Index

    The Upper Extremity Functional Index (ULFI) is a patient-reported outcome measure used to assess functional impairment in people with upper extremity musculoskeletal dysfunction. ULFI consists of 25 questions that assess the level of difficulty in performing activities of daily living using the upper extremities, including household and work activities, hobbies, lifting a bag of groceries, washing your scalp, pushing on your hands, driving, etc.

    10 minutes

Interventions

ObservationalOTHER

Psychometric properties will be assessed by administering the questionnaire online to approximately 200 participants. Reliability will be estimated by assessing stability and homogeneity.

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Healthy participants with myofascial pain.

You may qualify if:

  • shoulder pain
  • arm pain
  • myofascial pain
  • muscular pain
  • trigger points
  • arthritis

You may not qualify if:

  • tumor
  • metabolic disease
  • neurologic conditions

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Wounds and Injuries

Interventions

Watchful Waiting

Intervention Hierarchy (Ancestors)

Outcome Assessment, Health CareOutcome and Process Assessment, Health CareQuality of Health CareHealth Services Administration

Central Study Contacts

Jasemin Todri, PhD

CONTACT

+34 968 27 85 30jtodri@ucam.edu

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
7 Days
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

February 13, 2025

First Posted

February 19, 2025

Study Start

February 18, 2025

Primary Completion

February 28, 2025

Study Completion

March 15, 2025

Last Updated

February 19, 2025

Record last verified: 2025-02