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Self EfficacyNCT05614674

The Examination of Relationship Between Self-Efficacy in People With Chronic Low Back Pain

An observational study of Self Efficacy, run by Suleyman Demirel University.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Self-efficacy is defined as a person's confidence or belief that one can achieve a certain behavioral or cognitive state. Self-efficacy is one of the most important assesment parameters in the self-management model. Read more about this study

Who is it for?
Ages 30 to 65 yearsHealthy volunteers can take part
Conditions the study is for
Self Efficacy
How many people
162 participants
Where
No sites listed yet
Study dates
Nov 2022to May 2023
How long will I take part?
1 Day
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 30 to 65 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: Study group will consist of 30-65 years old people who will be agreed to take part in the study. There will be two groups. 1 of them is healthy group and the other is for people with low back pain. The partipicians will be literate enough to answer the questions in scales and questionnares by themselves

Who may be able to join

  • Being minimum 30 maximum 65 years old
  • To be literate
  • Accepting to take part in the study
  • Inclusion Criterias For Partipicians with Low Back Pain Group:
  • Being minimum 30 maximum 65 years old
  • Minimum 3 score from Visual Analog Scale (VAS)
Show all 9Show fewer
  • Having low back pain for at least 3 months of time
  • To be literate
  • Accepting to take part in the study

Who cannot join

  • Any kind of surgery in low back area
  • Surgery story in lower extremities
  • Acute low back pain
  • Having a neurological disorder
  • Having a rheumatological disease which may cause to low back pain
  • Having a herniated disc that presses on the sacral nerves
  • Being pregnant

Trial locations and contacts

No sites are listed yet.

Burak Kara, Bachelor contact

+905453765972

ptburakkara@gmail.com

About this study

Official title: The Examination of Relationship Between Self-Efficacy and Sensorial, Perceptual and Motor Skills in People With Chronic Low Back Pain A Cross-Sectional Study

Self-efficacy is defined as a person's confidence or belief that one can achieve a certain behavioral or cognitive state. Self-efficacy is one of the most important assesment parameters in the self-management model. It is accepted that patients with chronic low back pain with high self-efficacy have a better prognosis than those with low self-efficacy. Due to the complex nature of pain; The relationship between psychological and physical parameters such as pain catastrophy, disability level, depression, physical performance, self-efficacy, pain intensity and fear avoidance arouses curiosity. The aim of this cross-sectional study is to examine the relationship between the level of self-efficacy and sensory, perceptual and motor skills in people with chronic low back pain.

Conditions
Self Efficacy
Keywords
Back Pain, Propioception, Depression, Pain Catastrophizing, Flexibility, Balance
Medical subject headings
Back Pain, Depression

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT05614674
Study groupRoleWhat they receive
Healthy groupPeople who don't suffer from low back pain
People with low back painPeople who are suffering from low back pain. The pain level has to be at least 3 out of 10 according to Visual Analog Scale (VAS) to be in this group.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Visual Analog Scale (VAS)

    Measured: Baseline

  2. Pain Self-Efficacy Questionnaire (PSEQ)

    Measured: Baseline

  3. Proprioception Measurement with G-Pro Phone App

    Measured: Baseline

  4. Beck Depression Inventory (BDI)

    Measured: Baseline

  5. Pain Catastrophizing Scale (PCS)

    Measured: Baseline

  6. Sit and Reach Test (SRT)

    Measured: Baseline

  7. Multidirectional Reach Test

    Measured: Baseline

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted14 Nov 2022
  2. Study startNov 2022 (estimated)
  3. Primary completionJan 2023 (estimated)
  4. Study completionMay 2023 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Cross-sectional
Enrolment
162 participants (estimated)
Target duration
1 Day
IDs, dates and publications
ClinicalTrials.gov ID
NCT05614674
Sponsor's protocol ID
72867572-050.01.04-379338
Status last verified
Nov 2022
First submitted
5 Nov 2022
Last updated
14 Nov 2022
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Self Efficacy, run by Suleyman Demirel University.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 9 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 14 Nov 2022. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Burak Kara, Bachelor (+905453765972, ptburakkara@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Visual Analog Scale (VAS) (time frame: Baseline). The study lists 7 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Nov 2022.

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