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Responsiveness and Minimal Important Change of Two Measures of Pain Intensity in People With Low Back Pain

Responsiveness and Minimal Important Change of Two Measures of Pain Intensity in People With Low Back Pain

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06270069
Enrollment
150
Registered
2024-02-21
Start date
2024-03-01
Completion date
2025-02-28
Last updated
2024-02-21

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

Conditions

Low Back Pain

Brief summary

This is an observational study aimed at evaluating the responsiveness and minimal important change of two measures of pain intensity in people with low back pain. It consists of a battery of self-administered questionnaires which will be given to individuals with low back pain to complete before and after a rehabilitation treatment. Relationships among the different outcome measures will be also evaluated.

Detailed description

This is an observational study aimed at evaluating the responsiveness and minimal important change of two different graphical ways to assess pain intensity in people with low back pain. Literature found out that low back pain intensity is commonly assessed by a numerical rating scale ranging from no pain to the worst imaginable pain, once presented to responders horizontally. A different way to assess pain intensity could be to answer a similar numerical rating scale if set vertically. In Literature there are not studies which head-to-head evaluate the responsiveness and minimal important change of these two ways of assessing pain intensity due to low back pain. Participants will also have to complete self-reported outcome measures of disability, catastrophizing, fear of movement and self-efficacy, and correlations among these tools and the above two different ways to evaluate pain intensity will be evaluated. Descriptive statistics will be presented by taking into account the socio-demographic characteristics of the sample under investigation.

Interventions

OTHERExcercise-based therapy

An individual 60-min motor training sessions twice a week for eight-week outpatient program, that included exercises aimed at improving postural control, strengthening and stabilizing the back muscles, and stretching

Sponsors

International Institute of Behavioral Medicines
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Non specific low back pain * Adult age * Ability to understand the Italian language

Exclusion criteria

* Refuse to adhere to the study * Definite causes of low back pain * Central or peripheral neurological signs * Systemic illness or psychiatric deficits * Recent myocardial infarction, cerebrovascular events, or chronic lung or renal diseases

Design outcomes

Primary

MeasureTime frameDescription
NRSImmediately before the rehab treatment starts and immediately after the interventionNumerical Rating Scale; score 0-10 with higher estimates indicating higher levels of pain intensity (horizontal line)
Gauge of painImmediately before the rehab treatment starts and immediately after the interventionNumerical Rating Scale; score -5/+5 with lower estimates indicating higher levels of pain intensity (vertical line)

Secondary

MeasureTime frameDescription
TSKImmediately before the rehab treatment starts and immediately after the interventionTampa Scale of Kinesiophobia; score 13-52 with higher estimates showing higher fear of movement
ODIImmediately before the rehab treatment starts and immediately after the interventionOswestry Disability Index; score 0-50 with higher scores representing greater restriction to activities.
GPEImmediately after the interventionGlobal Perceived Effect (how much did the treatment received help your pain?); score -3 (it worsen a lot the things)/+3 (it helped a lot)
PSEQImmediately before the rehab treatment starts and immediately after the interventionPain Self Efficacy Questionnaire; score 0-60 with higher estimates showing higher self-effficacy
PCSImmediately before the rehab treatment starts and immediately after the interventionPain Catastrophizing Scale; score 0-52 with higher estimates showing higher catastrophizing

Contacts

Primary ContactBarbara Rocca, MSC
info.ellis.bm@gmail.com3333653393

Outcome results

None listed

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