The effect of physical educational program on Mental toughness, cognitive function, symptoms of related to MS and sleeping among ill people to MS

The effect and non- effect of physical educational program on Mental toughness, cognitive function, symptoms of related to MS (Fatigue, Paresthesia and depression ) and sleeping among ill people to multiple sclerosis (MS)

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2016062423705N4

Enrollment

Registered

2016-06-29

Start date

2016-06-22

Completion date

Unknown

Last updated

2018-02-22

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

Conditions

MS. multiple sclerosis

Interventions

Intervention 1: The experimental group underwent 8 weeks, 3 sessions per week 60 minutes exercise will do. Intervention 2: The control group will not receive any tests.

Behavior

The experimental group underwent 8 weeks, 3 sessions per week 60 minutes exercise will do

The control group will not receive any tests

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Inclusion criteria: has no cardiovascular illnesses, epilepsy, metabolic illnesses, Orthopedic illnesses, like Knee pain, and intend to partaking in study , Exclusion criteria: the maximum one on three of the exercising sessions do not do that and MS relapse during interference.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Cognitive function. Timepoint: The beginning of the study (baseline), week four and end of the study (week eight). Method of measurement: StroopTest.;Fatigue. Timepoint: The beginning of the study (baseline), week four and end of the study (week eight). Method of measurement: Fatigue Severity Scale (FSS).;Mental toughness. Timepoint: The beginning of the study (baseline), week four and end of the study (week eight). Method of measurement: Mental toughness questionnaire (MTQ48).;Paresthesia. Timepoint: The beginning of the study (baseline), week four and end of the study (week eight). Method of measurement: Visual Analogue Scale(VAS).;Depression. Timepoint: The beginning of the study (baseline), week four and end of the study (week eight). Method of measurement: Beck Depression Inventory (BDI).;Sleep. Timepoint: The beginning of the study (baseline), week four and end of the study (week eight). Method of measurement: Insomnia Severity Index (ISI).	—

Measure

Time frame

Cognitive function. Timepoint: The beginning of the study (baseline), week four and end of the study (week eight). Method of measurement: StroopTest.;Fatigue. Timepoint: The beginning of the study (baseline), week four and end of the study (week eight). Method of measurement: Fatigue Severity Scale (FSS).;Mental toughness. Timepoint: The beginning of the study (baseline), week four and end of the study (week eight). Method of measurement: Mental toughness questionnaire (MTQ48).;Paresthesia. Timepoint: The beginning of the study (baseline), week four and end of the study (week eight). Method of measurement: Visual Analogue Scale(VAS).;Depression. Timepoint: The beginning of the study (baseline), week four and end of the study (week eight). Method of measurement: Beck Depression Inventory (BDI).;Sleep. Timepoint: The beginning of the study (baseline), week four and end of the study (week eight). Method of measurement: Insomnia Severity Index (ISI).

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Sanobar Golshani

Kermanshah University of Medical Sciences

snb.gln@gmail.com+98 83 3826 4513

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026