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CompletedNCT04729218Updated Aug 2, 2022

The Movement Imagery Ability in Patients With Familial Mediterranean Fever

An observational study in Familial Mediterranean Fever, sponsored by Medipol University. Completed at 1 site in Turkey. Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-08-02.

Sponsored by Medipol University · Observational

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Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
60
Ages
18 Years to 65 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-14

Among 20 studies in Familial Mediterranean Fever with a site in Turkey — 7 open to participants now, 8 under way, none of them phase 3. Familial Mediterranean Fever · Turkey.

Enrollment
6th of 10
60 · median 80
Started
2018
with 1 other
Observational
10 of 20
4 open now
Registered
6th of 20
by date
Lead sponsor
1 of 20
Medipol University

Among the 20 studies in Familial Mediterranean Fever with a site in Turkey, this one is the 6th largest by enrollment of the 10 observational ones that give a count, is one of 2 that started in 2018, is one of 10 observational ones, and was the 6th registered.

Familial Mediterranean Fever

61 studies on the registry are indexed under Familial Mediterranean Fever; 27 are open to participants now.

Browse Familial Mediterranean Fever studies →

Open to participants now

7 of the 20 studies in Familial Mediterranean Fever with a site in Turkey are open now. Recruiting first, the newest first:

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All 7 open studies →

A study can be open while its sites in Turkey have not opened yet or have stopped. Only those recruiting at a site in Turkey →

Who these studies take

Of the 12 Familial Mediterranean Fever studies recruiting now, 4 (33%) set no upper age limit and 5 (42%) stop at 75 or younger; 10 take children under 18; 3 take healthy volunteers.

This study: 18 Years to 65 Years · all sexes · healthy volunteers too.

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02

Study summary

Motor imagery is the mental representation of movement without any doing body movement. A main function of imagery is to aid the self-regulation of thoughts, feelings, and behaviours. Studies have shown to be more effective for individuals displaying a higher level of imagery ability when using imagery to improve motor and motivational outcomes, including self-efficacy. The aim of this study is to measure the movement imagery ability in patients with Familial Mediterranean Fever and compare it with healthy individuals.

Read the detailed description

Familial Mediterranean Fever (FMF) is an autosomal recessive disease characterized by recurrent and self-limited attacks of fever associated with abdominal, chest, and joint pain. Previous studies have shown that individuals with FMF are more limited in terms of physical function than the normal population, and depression and anxiety are more common in these individuals. Being a lifetime disease, quality of life, and mental health can be affected due to serious complications such as attack frequency, disease resistance, and sometimes amyloidosis. Mental imagery is the ability to imaging the movement without doing the physical execution of the movement. During the last years, mental imagery is used in clinical practice as a tool for the treatment of chronic pain. Pain differs in patients with rheumatic diseases. Stress is one of the predictors of pain in patients with FMF. Even if the frequency is variable when attacks happen they may affect patients physically and their mental health and the ability to cope. A main function of imagery is to aid the self-regulation of thoughts, feelings, and behaviors. To use imagery for motor and motivational outcomes firstly the imagery ability levels should be measured.

03

Conditions studied

  • Familial Mediterranean Fever

Keywords

  • movement imagery ability
  • pain
  • catastrophizing
  • familial mediterranean fever
04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Patients with Familial Mediterranean Fever and Healthy Controls

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • having had at least one attack last year
  • co-operated individuals

Exclusion criteria

Exclusion Criteria:

  • patients with a neurological disorder,
  • diagnosed with cancer,
  • cognitive impairment,
  • having a primary pathology of the musculoskeletal system,
  • having previous imagery practice,
  • having an additional rheumatic disease
05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
60 participants (actual)
Patient registry
No

Groups and cohorts

  • Familial Mediterranean Fever group

    30 participants

    Behavioral: movement imagery ability

  • Healthy group

    30 participants

    Behavioral: movement imagery ability

Interventions

  • Behavioralmovement imagery ability

    Determining the movement imagery ability: internal visual, external visual and kinesthetic imagery

06

What researchers measure

Primary outcomes

  1. Movement Imagery Questionnaire-3 (MIQ-3)

    It is a questionnaire containing 12 items to evaluate the visual imagination skills of the individual. It evaluates internal visual imagery, external visual imagery, and kinesthetic imagery. For each item, first of all, individuals read the description of the movement, and then it is desired to perform the movement physically and after that, the same movement is requested. Individuals evaluate the degree of imagination on a 7-point Likert-type scale ranging from 1 (very difficult to see/feel) to 7 (very easy to see/feel). The motion visualization questionnaire has good psychometric properties, internal reliability, and estimated validity.

    Time frame: Baseline

Secondary outcomes

  1. McGill Melzack Pain Questionnaire (MPQ)

    MPQ consists of 78 descriptors grouped into four categories: sensory, affective, evaluative, and miscellaneous. These four categories were grouped into 20 subclasses each made up of 2 to 6 words according to pain intensity. Patients were asked to choose the pain descriptors according to the type of pain they felt during the attack episodes. Patients were instructed to choose one of the words that best described their type of pain experience. Changing of pain with time was assessed. Pain right now, pain at its worst and pain at its least was evaluated. Pain exacerbating or relieving factors were recorded.

    Time frame: Baseline

  2. Pain Catastrophizing Scale

    Pain Catastrophizing Scale identifies catastrophic thoughts or feelings and ineffective coping strategies of patients. PCS is a Likert-type self-assessment scale consisting of thirteen items. Each item is evaluated between 0 and 4 points. The total score ranges from 0 to 52. Includes rumination, magnification, and helplessness subscales. High scores indicate that the level of disaster is high.

    Time frame: Baseline

07

Study locations

1 site
  • Istanbul University, Cerrahpaşa Medical Faculty, Department of Rheumatology
    Istanbul, Turkey
08

References and documents

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Jan 2018 to primary completion in Feb 2021, 37 months.

How these figures are worked out, and which studies are left out of them.

Registered
Jan 24, 2021
First posted
Jan 28, 2021
StartActual
Jan 1, 2018
Primary completionActual
Feb 13, 2021
CompletionActual
Feb 18, 2021
Last update
Aug 2, 2022
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 2, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04729218
Lead sponsor
Medipol University
Responsible party
Albina Alikaj (Principal Investigator, Medipol University) — Principal investigator
First posted
Jan 28, 2021
Start date
Jan 1, 2018
Primary completion
Feb 13, 2021
Completion
Feb 18, 2021
Last update
Aug 2, 2022

Study contacts

Albina Alikaj, MSc
principal investigator · Medipol University
Ahsen Büyükaslan, MSc
study chair · Medipol University
Serdal Uğurlu, Prof
study director · Istanbul University - Cerrahpasa
Burcu Dilek, PhD
study director · Acibadem University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2022. You cannot join it, but the record below documents what was studied.

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