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Development of a Patient-reported Scale to Assess the Acceptability of Percutaneous Physiotherapy Interventions: a Modified Delphi Study

Development of a Patient-reported Scale to Assess the Acceptability of Percutaneous Physiotherapy Interventions: a Modified Delphi Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07380100
Acronym
Accept_scale
Enrollment
21
Registered
2026-02-02
Start date
2025-04-01
Completion date
2026-03-23
Last updated
2026-09-17

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

Conditions

Acceptability of Percutaneous Interventions

Keywords

Acceptability, Scale, Percutaneous Interventions

Brief summary

This study aims to develop a new evaluation tool to assess patient acceptability of percutaneous interventions. A Delphi methodology will be implemented, involving the recruitment of a panel of experts in percutaneous interventions and pain management. The scale will be developed through several iterative phases until a final version is reached, comprising clearly defined domains, subdomains, items, and questions to be answered by patients in order to obtain an overall acceptability score for the percutaneous technique received. The scale is intended to be applicable across a wide range of percutaneous interventions and, consequently, to a broad patient population undergoing different percutaneous treatments depending on their clinical condition.

Detailed description

This study aims to develop a new evaluation tool to assess patient acceptability of percutaneous interventions. A Delphi methodology will be implemented, involving the recruitment of a panel of experts in percutaneous interventions and pain management. The scale will be developed through several iterative phases until a final version is reached, comprising clearly defined domains, subdomains, items, and questions to be answered by patients in order to obtain an overall acceptability score for the percutaneous technique received. The scale is intended to be applicable across a wide range of percutaneous interventions and, consequently, to a broad patient population undergoing different percutaneous treatments depending on their clinical condition.

Interventions

OTHERIterative focus group sessions and individual evaluation phases

The expert panel conducted iterative focus group sessions and successive individual evaluation phases until consensus was reached on the development of the acceptability scale.

Sponsors

Universidad de Zaragoza
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

Experts were required to: * have at least five years of experience in percutaneous techniques * have clinical experience working with patients with pain

Design outcomes

Primary

MeasureTime frameDescription
Consensus among the expertsConsensus will be achieved through 5 evaluation phases: Day 1 and Day 7 after firstand second, respectively, focus group sessions Month 1, 2, 3, 4, and 5, after each individual evaluation roundConsensus must be achieved among the experts panel to establish final decisions on the acceptability scale development.

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 18, 2026