ClinicalTrials.gg
Not yet recruitingNCT07842744Updated Oct 8, 2026

Multiple Sclerosis Severity and Caregiver Health Outcomes

An observational study in Multiple Sclerosis, Caregiver Burden and Sleep Quality, sponsored by Süleyman Korkusuz. Not yet recruiting at 1 site in Turkey (Türkiye). Per ClinicalTrials.gov, last updated 2026-10-08.

Sponsored by Süleyman Korkusuz · Observational

Updated Sep 25, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
68
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 307 studies in Multiple Sclerosis with a site in Turkey — 59 open to participants now, 78 under way, 10 of them phase 3. Multiple Sclerosis · Turkey.

Planned enrollment
43rd of 103
68 · median 60
Started
2026
with 42 others
Observational
103 of 307
27 open now
Primary completion
2027-01
later than 61 of 77 live
Registered
302nd of 307
by date

Among the 307 studies in Multiple Sclerosis with a site in Turkey, this one is the 43rd largest by planned enrollment of the 103 observational ones, is one of 43 that started in 2026, is one of 103 observational ones, reaches primary completion later than 61 of the 77 other live ones, and was the 302nd registered.

By phase

307 studies; the count open now beside each. This study's row is marked.

No phase155 · 31 open
Observationalthis study103 · 27 open
Phase 340 · 1 open
Phase 26 · 0 open
Phase 43 · 0 open

By the year they started

First in 2004; this study’s year is marked. 43 started in 2026.

Size and results

Median enrollment 40 across the 204 interventional studies, 60 across the 103 observational. Of the 204 that completed or were terminated, 37 (18%) have results posted.

Was this useful?
Watch this landscapeDownload CSVWith an account: a weekly mail of what changed among 307 studies in Multiple Sclerosis with a site in Turkey, or all of them as a file.
02

Study summary

This cross-sectional observational study aims to investigate the associations between multiple sclerosis (MS) severity and caregivers' sleep quality, physical activity, body awareness, perceived stress, and caregiver burden. A total of 68 caregivers of patients with MS will be recruited from Başkent University Hospital. MS severity will be assessed using the Expanded Disability Status Scale (EDSS), while caregiver health outcomes will be evaluated using validated questionnaires. The findings are expected to provide insight into the multidimensional impact of MS severity on caregiver health and well-being.

Read the detailed description

This cross-sectional observational study aims to investigate the associations between multiple sclerosis (MS) severity and caregivers' sleep quality, physical activity, body awareness, perceived stress, and caregiver burden.

A total of 68 caregivers of individuals with MS will be included. Disease severity will be assessed using the Expanded Disability Status Scale (EDSS). Caregiver outcomes will be evaluated using the Pittsburgh Sleep Quality Index (PSQI), International Physical Activity Questionnaire-Short Form (IPAQ-SF), Body Awareness Questionnaire (BAQ), Perceived Stress Scale (PSS), and Zarit Burden Interview (ZBI).

The study will examine the relationships between MS severity and caregiver health outcomes within the framework of the International Classification of Functioning, Disability and Health (ICF). No therapeutic intervention will be administered.

03

Conditions studied

  • Multiple Sclerosis
  • Caregiver Burden
  • Sleep Quality
  • Physical Activity
  • Psychological Stress
04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

The study population will consist of 68 adult caregivers of individuals diagnosed with multiple sclerosis who receive care at Başkent University Hospital. Caregivers will be recruited to evaluate the associations between MS severity and caregiver health outcomes.

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

  • Being 18 years of age or older.
  • Providing regular care to an individual diagnosed with multiple sclerosis for at least six months.
  • Volunteering to participate in the study.

Exclusion criteria

Exclusion Criteria:

  • Having a cognitive impairment that prevents completion of the assessments.
  • Having a severe physical or psychiatric condition that may interfere with study assessments.
  • Being unable to complete the questionnaires.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
68 participants (estimated)
Patient registry
No

Groups and cohorts

  • Caregivers of Patients With Multiple Sclerosis

    Adult caregivers who have provided regular care to a person diagnosed with multiple sclerosis for at least six months.

06

What researchers measure

Primary outcomes

  1. Caregiver Burden (Zarit Burden Interview)

    Caregiver burden will be assessed using the Zarit Burden Interview (ZBI). Higher scores indicate greater perceived caregiver burden.

    Time frame: Baseline

Secondary outcomes

  1. Sleep Quality (Pittsburgh Sleep Quality Index)

    Sleep quality will be assessed using the Pittsburgh Sleep Quality Index (PSQI). Total scores range from 0 to 21, with higher scores indicating poorer sleep quality. Scores above 5 indicate poor sleep quality.

    Time frame: Baseline

  2. Physical Activity (IPAQ-SF)

    Physical activity will be assessed using the International Physical Activity Questionnaire-Short Form (IPAQ-SF). Total physical activity will be expressed as metabolic equivalent of task minutes per week (MET-min/week) based on activities performed during the previous seven days. Total MET-min/week is calculated as the sum of walking (3.3 METs × minutes × days), moderate-intensity activity (4.0 METs × minutes × days), and vigorous-intensity activity (8.0 METs × minutes × days). The minimum possible value is 0 MET-min/week; there is no fixed maximum score. Higher MET-min/week values indicate a higher level of physical activity and therefore a better outcome.

    Time frame: Baseline

  3. Body Awareness (Body Awareness Questionnaire)

    Body awareness will be assessed using the 18-item Body Awareness Questionnaire (BAQ). Each item is rated on a 7-point Likert scale from 1 to 7, yielding a total score ranging from 18 to 126. Higher scores indicate greater body awareness and therefore a better outcome

    Time frame: Baseline

  4. Perceived Stress (Perceived Stress Scale)

    Perceived stress will be assessed using the 10-item Perceived Stress Scale (PSS-10). Total scores range from 0 to 40, with higher scores indicating greater perceived stress.

    Time frame: Baseline

07

Study locations

1 site
08

References and documents

Publications

  • Khan F, Pallant J, Brand C. Caregiver strain and factors associated with caregiver self-efficacy and quality of life in a community cohort with multiple sclerosis. Disabil Rehabil. 2007 Aug 30;29(16):1241-50. doi: 10.1080/01443610600964141. PubMed 17653999 ↗
  • Maguire R, Maguire P. Caregiver Burden in Multiple Sclerosis: Recent Trends and Future Directions. Curr Neurol Neurosci Rep. 2020 May 22;20(7):18. doi: 10.1007/s11910-020-01043-5. PubMed 32444986 ↗

Individual participant data

Plan to share: No

09

Timeline

2 registry updates since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Oct 2026; primary completion for Jan 2027, 3 months later.

Of 334 non-industry observational studies under Multiple Sclerosis, half reached primary completion within 36 months of starting (the median), counting those still running; a quarter within 13 and three quarters within 73. This study's planned 3 months is below that.

Counting every sponsor, half of 425 studies reached it within 41 months; a quarter within 15 and three quarters within 75.

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

Registered
Sep 21, 2026
First posted
Sep 25, 2026
StartEst.
Oct 20, 2026
Primary completionEst.
Jan 20, 2027
CompletionEst.
Feb 20, 2027
Last update
Oct 8, 2026
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.
Secondary outcomes
2 description edited
What changed in the outcomes
  • DescriptionBody Awareness (Body Awareness Questionnaire): how it is measured was reworded
  • DescriptionPhysical Activity (IPAQ-SF): how it is measured was reworded
Oct 8, 2026
Registered
First appeared on the registry
Sep 25, 2026
Show all 2 updates
  1. Oct 8, 2026
    Secondary outcomes 2 description edited
    What changed in the outcomes
    • DescriptionBody Awareness (Body Awareness Questionnaire): how it is measured was reworded
    • DescriptionPhysical Activity (IPAQ-SF): how it is measured was reworded
    + 1 other change: verification date
  2. Sep 25, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07842744
Lead sponsor
Süleyman Korkusuz
Responsible party
Süleyman Korkusuz (Assist. Prof. Dr, Atılım University) — Sponsor-investigator
First posted
Sep 25, 2026
Start date
Oct 20, 2026 (estimated)
Primary completion
Jan 20, 2027 (estimated)
Completion
Feb 20, 2027 (estimated)
Last update
Oct 8, 2026

Study contacts

Süleyman Korkusuz, PhD
Contact
suleyman.korkusuz@atilim.edu.tr
+905388675480
Büşra S Korkusuz
study chair · Ankara University
Cemre Yılmaz
study chair · Atılım University
Süleyman Korkusuz
principal investigator · Atılım 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 not yet recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion