The Effect of Telerehabilitation on Pain, Physical and Biopsychosocial Factors in Parent Carers

NCT ID: NCT06518811

Last Updated: 2025-08-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-12-12

Study Completion Date

2023-06-20

Brief Summary

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This study aimed to investigate the effects of asynchronous video-based exercises on pain, disability, anxiety, care burden and quality of life in parent carers of children with special needs.

Detailed Description

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This study aimed to investigate the effects of asynchronous video-based exercises on pain, disability, anxiety, care burden and quality of life in parent carers of children with special needs.

Parents carers were invited to participate in the study through a variety of channels, including printed posters, corporate social media posts, phone calls through local administrations and non-governmental associations. At the information meeting, the participants were informed about the benefits of ergonomic training for activities of daily living. Also handbooks containing the same information were distributed. Demographic data were collected, and questionnaires were used to assess pain, disability, physical activity levels, care burden, and quality of life.

Individuals who met the inclusion criteria were randomly assigned to either the exercise group or the control group. The exercise group was informed of the details of the study methodology, technology literacy, and tablet usage. In order to ascertain an appropriate exercise programme for each individual, the researchers identified musculoskeletal problems of participants. The exercise programme comprised videos of relaxation, postural control and muscle strengthening exercises, which were recorded by research team and uploaded to the tablets. Subsequently, the participants were informed of the safety precautions during the exercise programme at home and the ergonomic placement of the tablets.

The eight-week exercise programme required participants to perform the exercises on a regular basis, three times per week, with the assistance of guided videos. Additionally, they were required to record their performance in written exercise diaries, which were distributed to them.

Exercises also supported by online calls made by the researchers once a week. In each interview, the participants were reminded of the next scheduled online interview activity. At the end of the eight-week, final evaluations were obtained through face-to-face interviews.

Conditions

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Muskuloskeletal Diseases

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

OTHER

Blinding Strategy

SINGLE

Participants
Eligible individuals will be randomly allocated to either the exercise group or the control group. Participants will be blinded to their group assignment.

Study Groups

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Exercise group

The asynchronous video-based telerehabilitation programme had a duration of eight weeks. The exercise group participants were instructed to perform the exercises on a regular basis, three days a week, with a time interval of 24 hours between each session. The exercises were to be performed using the instructional videos and recorded in the exercise diaries provided.

Group Type EXPERIMENTAL

Video-Based Exercise Programme

Intervention Type OTHER

The asynchronous video-based telerehabilitation programme had a duration of eight weeks. The participants were instructed to perform the exercises on a regular basis, three days a week, with a time interval of 24 hours between each session. The exercises were to be performed using the instructional videos and recorded in the exercise diaries provided. The participants were used exercise balls and resistance bands distributed by the researchers according to exercise programme.

Control group

Control group participants were informed about the benefits of ergonomic training for activities of daily living. Also handbooks containing the same information were distributed.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Video-Based Exercise Programme

The asynchronous video-based telerehabilitation programme had a duration of eight weeks. The participants were instructed to perform the exercises on a regular basis, three days a week, with a time interval of 24 hours between each session. The exercises were to be performed using the instructional videos and recorded in the exercise diaries provided. The participants were used exercise balls and resistance bands distributed by the researchers according to exercise programme.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* The individual must be the primary caregiver of a child with physical, mental, or a combination of both disabilities.
* The individual must have been in this role for a minimum of six months.
* Willing to participate in the study.
* Able to read and write in Turkish.

Exclusion Criteria

* A clear cognitive or language disability
* A recent deterioration of family relationships or the presence of factors affecting them (separation of parents, divorce, etc.)
* A history of cardiac or pulmonary disease or diseases (uncontrolled hypertension, arrhythmia, COPD, asthma, etc.), neurological disease, orthopaedic or rheumatological disease (rheumatoid arthritis, ankylosing spondylitis, arthrosis, etc.)
* A disease that may prevent exercise or that has resulted in surgery
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Ilke KARA

OTHER

Sponsor Role lead

Responsible Party

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Ilke KARA

Co-Investigator

Responsibility Role SPONSOR_INVESTIGATOR

Locations

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Dokuz Eylul University

Izmir, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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DEU-FTR-IK-03

Identifier Type: -

Identifier Source: org_study_id

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