Investigating the effect of surface Stroking technique in pain severity on Arthroscopic knee surgery patients.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT201108196973N3

Enrollment

Registered

2011-09-03

Start date

2009-10-02

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

musculoskeletal and joint disorder. Diseases of the musculoskeletal system and connective tissue

Interventions

Intervention 1: Intervention group: surface stroking massage, a 20-minute session, surface stroking massage is no drug intervention including use of whole palmar hands on patient’s skin surface and to

Rehabilitation

Intervention group: surface stroking massage, a 20-minute session, surface stroking massage is no drug intervention including use of whole palmar hands on patient’s skin surface and touch the skin fro

Control group: Routine activities

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Inclusion criteria: Willingness to participate, ability to do surface Stroking massage under physician order, ability to read and write Exclusion criteria: Presence of other diseases such as mental disorder, past history of participating in a surface Stroking massage, cognitive disorder, addiction, other neurological disorders

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Pain severity. Timepoint: Befor and after intervention. Method of measurement: ten nominal pain scale questionnaire.	—

Secondary

Measure	Time frame
Blood pressure. Timepoint: Befor and after intervention. Method of measurement: patient monitoring system.;Respiratory rate. Timepoint: Befor and after intervention. Method of measurement: patient monitoring system.;Puls rate. Timepoint: Befor and after intervention. Method of measurement: patient monitoring system.;Anxiety. Timepoint: Befor and after intervention. Method of measurement: Hamilton anxiety questionnaire.;Patient sleep pattern. Timepoint: Befor and after intervention. Method of measurement: Self report questionnaire.	—

Measure

Time frame

Blood pressure. Timepoint: Befor and after intervention. Method of measurement: patient monitoring system.;Respiratory rate. Timepoint: Befor and after intervention. Method of measurement: patient monitoring system.;Puls rate. Timepoint: Befor and after intervention. Method of measurement: patient monitoring system.;Anxiety. Timepoint: Befor and after intervention. Method of measurement: Hamilton anxiety questionnaire.;Patient sleep pattern. Timepoint: Befor and after intervention. Method of measurement: Self report questionnaire.

—

Countries

Iran (Islamic Republic of)

Contacts

Public Contacthedayat alah lalegani

Shahrekord University of Medical Sciences and Health Services

lalegani@skums.ac.ir+98 38 1333 5653

Outcome results

None listed

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