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Evaluation The Effect Of The Fordyce Happiness Program On sleep Quality,Spiritual Well-Being ,and Pain In Peoples With Multiple Sclerosis

Evaluation The Effect Of The Fordyce Happiness Program On sleep Quality,Spiritual Well-Being ,and Pain In Peoples With Multiple Sclerosis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20091215002861N11
Enrollment
70
Registered
2017-12-12
Start date
2016-09-22
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

Multiple Sclerosis. Demyelinating diseases of the central nervous system

Interventions

Intervention 1: after obtaining the consent from from trial group, fordyce happiness program carried out in 8 sessions of 60 minutes once a week and happy principle taught with 14 element. Specified g
Behavior
after obtaining the consent from from trial group, fordyce happiness program carried out in 8 sessions of 60 minutes once a week and happy principle taught with 14 element. Specified goals and tasks f
In the control group during the routine activities are follow-up and after the collection of questionnaires in in both groups, fordyce happiness program was taught in two sessions in the control group

Sponsors

Sponsor 1 Vice chancellor for research of Shahrekord University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria:

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Spiritual Well-Being. Timepoint: Baseline; Imediately After; 2 months After. Method of measurement: Spiritual Well-Being Scale.;Sleep Quality. Timepoint: Baseline; Imediately After; 2 months After. Method of measurement: Pitsburgh Sleep Quality Index.;Pain. Timepoint: Baseline; Imediately After; 2 months After. Method of measurement: Visual Analogue scale.

Secondary

MeasureTime frame
Quality of life. Timepoint: 6months After intervention. Method of measurement: SF-36 Standard Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactkobra zaheri

Shahrekord University of Medical Sciences

kobrazaheri1988@gmail.com+98 33389760

Outcome results

None listed

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