Skip to content

Teleeducation and therapeutic physical exercise intervention program, group-based and remote, for family caregivers. Randomized controlled trial

Teleeducation and therapeutic physical exercise intervention program, group-based and remote, for family caregivers. Randomized controlled trial assessing the effect on musculoskeletal pain

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12625001357448
Enrollment
48
Registered
2025-12-03
Start date
2026-01-15
Completion date
2026-02-15
Last updated
2025-12-08

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

Conditions

None listed

Brief summary

A distance-based, group-based therapeutic physical exercise intervention program was developed and supervised by a physical therapist from the research group. The results will be analyzed jointly to assess the program's impact. The pretest-posttest design will allow for a comparative evaluation using validated scales before and after the intervention in both groups, thus allowing for an assessment of the impact obtained.

Interventions

A quasi-experimental design with an experimental group and a control group is proposed, longitudinal and prospective. The experimental group will receive a tele-education program in health combined with therapeutic exercise, while the control group will only participate in the tele-education program. Participants will be assigned to each group using balanced randomization, performed using free software (http://www.randomized.org/). Only the principal investigator will be aware of the randomizati

A quasi-experimental design with an experimental group and a control group is proposed, longitudinal and prospective. The experimental group will receive a tele-education program in health combined with therapeutic exercise, while the control group will only participate in the tele-education program. Participants will be assigned to each group using balanced randomization, performed using free software (http://www.randomized.org/). Only the principal investigator will be aware of the randomization sequence. The experimental group will participate in a distance-based group therapeutic physical exercise intervention program, developed and supervised by a physical therapist from the research group. The Remote Group Therapeutic Physical Exercise Intervention Program will consist of 15 guided 60-minute therapeutic physical exercise sessions distributed over 3 weekly sessions for 5 weeks. All participants will attend the same group. An attendance checklist for the sessions will be included. Will include spinal mobility exercises, core strength training, scapular mobility and stability, upper body and lower body mobility and strength training, as well as breathing exercises. These exercises will combine Pilates exercises, basic strength and mobility exercises, and relaxation and breathing. Participants will not need any specific equipment to perform the exercises. The difficulty of the exercises will increase throughout the sessions in three levels: basic 1, basic 2, and intermediate, allowing you to progress through the exercises toward a heavier load, a greater range of motion, or greater complexity, seeking more complex muscle synergies. The Therapeutic Physical Exercise Program will always be carried out in the same order and with the same structure. Sessions will be conducted in groups, via video calls, and will be led by a physical therapist who will pay special attention to the individual needs of each participant. The difficulty of the exercises will increase as the program progresses. The Therapeutic Physical Exercise Program has been designed based on the literature and will take into account the conditions of the experimental group. To measure outcomes, selected participants, once they meet the inclusion and exclusion criteria, will be evaluated before the intervention and four week after the end of the last session. The results obtained will be analyzed jointly to assess the program's impact. The pretest-posttest design will allow for a comparative evaluation using scales validated before and after the intervention in both groups, thus allowing for an assessment of the impact achieved.

Sponsors

University of Seville
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Primary purpose
Treatment
Masking
Blinded (masking used) (Subject)

Eligibility

Sex/Gender
All
Age
18 Years to 67 Years
Healthy volunteers
Yes

Inclusion criteria

Caregivers of a person with recognized total or severe dependency, between 18 and 67 years of age, family caregivers of a dependent person over 67 years of age, with a dedication of six hours per day to the person, and individuals in good physical health and with basic knowledge of how to use social media.

Exclusion criteria

People who do not speak Spanish well enough to understand the study guidelines and answer the questionnaires provided, and family caregivers of people with cancer or mental health conditions.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026