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Transcultural Adaptation and Validation to Spanish of the OSPRO Questionnaires

Transcultural Adaptation and Validation to Spanish of the Optimal Screening for Prediction of Referral and Outcome (OSPRO) Questionnaires for Review-Of-Systems (OSPRO-ROS) and Yellow-Flags (OSPRO-YF) in Subjects With Musculoskeletal Pain.

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05869695
Acronym
SpanishOSPRO
Enrollment
200
Registered
2023-05-22
Start date
2020-11-30
Completion date
2024-06-30
Last updated
2023-05-22

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

Conditions

Musculoskeletal Pain

Keywords

OSPRO, Review of Systems, Red Flags, Psychosocial factors, Yellow Flags, Cross-cultural, Reliability, Validity

Brief summary

Clinical guidelines for managing musculoskeletal pain recommend first, assessing and identifying any signs of severe physical conditions (i.e.red flags) and then, asessing the psychosocial prognostic factors of poor outcomes (i.e.yellow flags). The Optimal Sreening for Prediction of Referral and Outcome (OSPRO) cohort studies were designed to develop and validate standard assessment tools for Review Of Systems (OSPRO-ROS) and Yellow Flags (OSPRO-YF).

Detailed description

The objectives of this study were to translate and cross-cultural adapt OSPRO-ROS and OSPRO-YF questionnaires to Spanish and to investigate their psychometric properties for their use in subjects with musculoskeletal pain.To accomplish the objectives proposed, this study was developed in two phases:Phase I: Cross-cultural adaptation process.Phase II: Psychometric properties evaluation.

Interventions

OTHEROSPRO-ROS Questionnaire

Completion of questionnaires

OTHEROSPRO-YF Questionnaire

Completion of questionnaires

Sponsors

University of Alcala
CollaboratorOTHER
Escoles Universitaries Gimbernat
CollaboratorOTHER
Hospital ASEPEYO Sant Cugat
CollaboratorUNKNOWN
Consorci Sanitari de Terrassa
CollaboratorOTHER
University of Valencia
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

OSPRO-ROS: 1. Were coming to the emergency department on their first visit. 2. With acute musculoskeletal pain. 3. Were able to read and comprehed Spanish language. OSPRO-YF: 1. Were seeking outpatient physical therapy treatment. 2. With chronic musculoskeletal pain involving the cervical spine, lumbar spine, shoulder or knee. 3. Were able to read and comprehend Spanish language.

Exclusion criteria

1. Widespread chronic pain syndrome (e.g. fibromyalgia or irritable bowel syndrome). 2. Neuropathic pain syndrome (e.g. complex regional pain syndrome or diabetic neuropathy). 3. Psychiatric history (currently in care of mental health care provider or taking \> 2 precription psychiatric medications) 4. Cancer (currently receiving treatment for active cancer) 5. Neurological disorder (e.g. stroke, spinal cord injury, or traumatic brain injury).

Design outcomes

Primary

MeasureTime frameDescription
Patient-Reported Outcome Measure (PROM) development: Translation and Cross Cultural Adaptation to the Spanish population of the Optimal Screening for Prediction of Referral and Outcome (OSPRO) questionnaires.from September 2018 to July 2021Two native Spanish speakers, health experienced in musculoskeletal pain and knowledge of English, translated into Spanish the Optimal Screening for Prediction of Referral and Outcome-Review of Systems (OSPRO-ROS) questionnaire original (English) and the Optimal Screening for Prediction of Referral and Outcome Yellow-Flags (OSPRO-YF) original questionnaire (English). Two native English speakers, knowledge of Spanish, reverse-translate the text to Spanish. 25 participants with musculoskeletal pain completed the Optimal Screening for Prediction of Referral and Outcome (OSPRO) questionnaires. This outcome will be evaluated according the Consensus-based Standards for the selections of health Measurement Instruments (COSMIN) Risk of Bias checklist for PROMs, using their scoring manual: very good/adequate/doubtful/inadequate/NA for each standar.

Secondary

MeasureTime frameDescription
OSPRO questionnaires Psychometric property Validationfrom January to June 2024The validity and reliability of the Spanish version translated from the questionnaires Optimal Screening for Prediction of Referral and Outcome (OSPRO) will be assessed. This outcome will be evaluated according the Consensus-based Standards for the selections of health Measurement Instruments (COSMIN) Risk of Bias checklist for PROMs, using their scoring manual: very good/adequate/doubtful/inadequate/NA for each standar.

Countries

Spain

Contacts

Primary ContactMELÀNIA MASÓ NÚÑEZ
melania.maso@eug.es+34935893727
Backup ContactMARTA TELLO FONTANET
MTello@CST.cat+34937003608

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026