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RecruitingNCT07261553Updated Mar 25, 2026

Adherence to Home-Based Exercises in Musculoskeletal Disorders

An observational study in Exercise Training, Adherence, Treatment and Musculoskeletal Disease, sponsored by Konya Beyhekim Training and Research Hospital. Recruiting at 1 site in Turkey (Türkiye). Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-03-25.

Sponsored by Konya Beyhekim Training and Research Hospital · Observational

From the registry’s dates

  • Primary completion was expected by Apr 2026, 6 months ago, but the record still lists the study as recruiting.
  • Started Dec 2024; still recruiting 1 year 9 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
252
Ages
18 Years and older
Sex
All
01

Study summary

Home exercise program is recommended by physicians to patients and their relatives to do at home and It is a treatment option in which the physician describes how to do it. Home workout program to be completed at home to complement and reinforce their program in the clinic It is a personalized set of therapeutic exercises that are taught. There are factors that can change exercise compliance; There are some reasons why some patients adhere to the prescribed home exercise program and others do not.

Adherence to home exercises is a major issue in rehabilitation and the reasons for this are multifactorial; It includes both psychological and specific conditions factors that vary between each individual and these conditions should be taken into account by clinicians in designing personalized exercise programs.

Home exercise programs constitute a fundamental component of rehabilitation and are widely prescribed by physicians support therapeutic gains beyond the clinical environment. These individualized programs aim to maintain functional improvements, reduce symptoms, and promote self-management among individuals with musculoskeletal disorders. Although adherence to home-based exercises is recognized as a key determinant of rehabilitation outcomes, non-adherence remains a persistent challenge. Despite growing emphasis on the importance of exercise compliance, the existing literature provides relatively limited and insufficient evidence regarding the factors that influence adherence across different musculoskeletal conditions, including degenerative, orthopedic, and neurological disorders.

Addressing this gap, the present prospective longitudinal cohort study aims to evaluate adherence to individualized home-based exercise programs among patients with diverse musculoskeletal conditions and to determine whether adherence behaviors differ across diagnostic groups. In addition, the study seeks to identify demographic, clinical, psychosocial, and functional factors associated with exercise compliance. By integrating structured clinical evaluations with validated outcome measures, this study aims not only to clarify the determinants of exercise adherence but also to contribute to the development of more effective, condition-specific strategies to enhance sustained engagement in home-based rehabilitation.

Read the detailed description

Home exercise programs are recommended by physicians to patients and when appropriate, their caregivers as interventions to be performed outside the clinical setting. In this treatment approach, the physician provides detailed instructions on how the exercises should be carried out. These programs consist of individualized therapeutic exercises designed to be performed at home, with the aim of complementing and reinforcing the interventions delivered in the clinic. Addressing this gap, the present study aims to evaluate adherence to individualized home-based exercise programs among patients with diverse musculoskeletal conditions and to determine whether adherence behaviors differ across diagnostic groups. In addition, the study seeks to identify demographic, clinical, psychosocial, and functional factors associated with exercise compliance. By integrating structured clinical evaluations with validated outcome measures, this study aims not only to clarify the determinants of exercise adherence but also to contribute to the development of more effective, condition-specific strategies to enhance sustained engagement in home-based rehabilitation.

Meeting the inclusion and exclusion criteria; various musculoskeletal diseases; Patients presenting for degenerative, orthopedic or neurological rehabilitation will be included in the study by obtaining written informed consent after an individualized home exercise program after a detailed clinical examination.

Questions such as age, gender, height, weight, education level, employment status, income level and sociodemographic and clinical characteristics of the participants (diagnosis of the disease, duration, comorbidity/cumulative disease score status, medical treatment status, if any, pain/weakness level, functional status) will be recorded.

All patients will receive an individualized home exercise program based on their clinical condition. Exercises will be determined by the physical therapy and rehabilitation physician, taking into account the minimum clinical needs and individual characteristics of the patient. People receiving active physical therapy; will not be included in the study. In terms of content, general physical therapy will consist of exercises, not specific exercises that are rarely practiced or performed by a health professional. The number of sets of exercises per day, how many times they will be done in each set and how many days a week will be defined and recorded. The exercises will be explained to the patient by the physician and the printed paper describing these exercises will be given to the patient.

Three condition-specific subcohorts will be defined: chronic degenerative, orthopedic (post-operative) and neurological patients. Patients in the degenerative, orthopedic, or neurological rehabilitation groups will be provided with a patient-specific home exercise program, and their adherence and adaptations to the program will be evaluated and compared. Patients will do the home-based exercise program for 6 weeks. Patients will undergo both clinical and outcome-based assessments at baseline and again at the completion of the home exercise program (6 weeks).

Among the result criteria; Primary variables; Beck Depression Index (BDI) for mood, Health Assessment Questionnaire (HAQ) for quality of life, Kinesiophobia assessment; Tampa Kinesiophobia Scale, Visual Analog Scale (VAS 0-10), for Activities of Daily Living; Barthel Activities of Daily Living Index Secondary variables; to assess how an individual's health condition affects their daily life for exercise adherence; The Exercise Adherence Rating Scale/Exercise Attitude Questionnarie. All assessments will be evaluated by a group-blind investigator after 6 weeks with clinical examination and a set of evaluation scales/questionnaires. The patients' clinical status, satisfactions, their adherence to exercise therapy, and the factors influencing this adherence will be evaluated. Patients whose diagnosis was established after a detailed examination and for whom an exercise program was prescribed will be included in the study. The decision will be based solely on the patient's ability to perform the exercises and adherence to the inclusion and exclusion criteria. Other factors that could potentially introduce bias, such as education level or the patient's willingness to exercise, will not be considered in determining treatment, in order to minimize selection bias. Patients will be instructed not to take any analgesics within 24 hours prior to the assessment.

02

Conditions studied

  • Exercise Training
  • Adherence, Treatment
  • Musculoskeletal Disease
  • Rehabilitation Exercise
  • Adherence, Patient
  • Home Exercise Program
  • Stroke
  • Orthopedic Operations
  • Degeneration of Spine and Osteoarticular

Keywords

  • Home Exercise Program
  • adherence
  • Rehabilitation Exercise
  • Musculoskeletal Disease
  • Adherence, Patient
03

In context

Treatment Adherence and Compliance

114 studies on the registry are indexed under Treatment Adherence and Compliance; 60 are open to participants now.

This study's planned enrollment of 252 is below the median of 281 across 17 observational studies indexed under Treatment Adherence and Compliance.

Browse Treatment Adherence and Compliance studies →

Lead sponsor

Konya Beyhekim Training and Research Hospital is the lead sponsor of 31 studies on the registry; 15 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

  • Be 18 years of age or older
  • To have a musculoskeletal disease (degenerative, neurological or orthopedic)
  • To be given a home exercise program
  • To have cognitive and language functions to communicate, to be a volunteer

Inclusion criteria

  • Be 18 years of age or older
  • To have a musculoskeletal disease (degenerative, neurological or orthopedic)
  • To be given a home exercise program
  • To have cognitive and language functions to communicate, to be a volunteer

Exclusion criteria

Exclusion criteria:

  • Those with major psychiatric illness
  • Those with cognitive dysfunction
  • Those with communication disorders, reluctant/reluctant to participate
  • Those with any condition other than a primary degenerative, orthopedic, or neurological disease that could significantly affect exercise adherence, including musculoskeletal or systemic disorders (e.g., severe anemia, heart failure, respiratory failure, uncontrolled diabetes, inflammatory rheumatic disease, recent fractures, or active infections).
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
252 participants (estimated)
Patient registry
No

Groups and cohorts

  • Degenerative rehabilitation

    Patients with chronic degenerative musculoskeletal disorders, including nonspecific low back pain, chronic nonspecific neck pain, and knee osteoarthritis, receiving a home-based exercise program (subcohort)

    Other: Home exercise program

  • Orthopedic rehabilitation

    Patients receiving a home exercise program as part of post-operative orthopedic rehabilitation, including rehabilitation following rotator cuff repair, total knee arthroplasty, and lumbar spinal surgery (subcohort).

    Other: Home exercise program

  • Neurological

    Patients receiving a home-based exercise program following a neurological condition (stroke, hemiplegia) as part of neurological rehabilitation (subcohort).

    Other: Home exercise program

Interventions

  • OtherHome exercise program

    Patients with chronic degenerative musculoskeletal disorders receiving a home exercise program

  • OtherHome exercise program

    Patients receiving a home exercise program as part of post-operative orthopedic rehabilitation

  • OtherHome exercise program

    Patients receiving a home exercise program following a neurological condition (stroke,hemiplegia) as part of rehabilitation

06

What researchers measure

Primary outcomes

  1. Exercise Adherence Rating Scale

    It was developed to evaluate compliance with home exercise programs. The first part (Group A) contains the participant's general information about the exercise program; the second part (Group B; 0-24 points) examines the frequency and sustainability of exercise behaviors; the third part (Group C; 0-40 points) evaluates cognitive and environmental factors affecting exercise adherence. The total score ranges from 0-64, with higher scores indicating greater compliance. The Turkish adaptation, including validation and reliability analysis, was conducted in 2019.

    Time frame: 6th week

Secondary outcomes

  1. VAS

    VAS ; patients were asked to mark their pain intensity pain activity and rest: 0 no pain; 10 Unbearable/Max. Pain. Ranges for the severity of pain and weakness; \<3 mild, 3-6 moderate, \>6 severe.

    Time frame: Baseline and 6th week

  2. Beck Depression Index

    BDI consists of 21 items related to depressive symptoms such as pessimism, sense of failure, dissatisfaction, feelings of guilt, restlessness, fatigue, decreased appetite, indecision, sleep disturbance, and social withdrawal. Each item contains four levels (0-3) self-evaluation statements that determine a behavior specific to depression . The total maximum score was 63, and a score above 17 indicates an increased risk of depressive states.

    Time frame: Baseline and 6th week

  3. Barthel Index

    Barthel Index is a general scale developed for independence in activities of daily living. It consists of 10 questions. In the scoring ranging from 0-100 points, 100; best complete independence, 0; the worst refers to absolute dependence.

    Time frame: Baseline ve 6th week

  4. Tampa Kinesiophobia Scale

    Tampa Kinesiophobia Scale ; is a 17-question scale developed to measure the fear of movement/re-injury. The scale includes parameters for injury/re-injury and fear-avoidance in work-related activities. A 4-point Likert scoring (1= Strongly disagree, 4= Completely agree) is used in the scale. A total score is calculated after reversing items 4, 8, 12 and 16. The person gets a total score between 17-68. The higher the score of the person on the scale, indicates that kinesiophobia is also high.

    Time frame: Baseline and 6th week

  5. Health assessment questionnaire

    Health assessment questionnaire (HAQ) is the most widely used disease-related, short, easy-to-apply quality of life scale used in clinical research. The scale consists of a total of 21 questions in 8 sub-headings. Each question has a likert type option ranging from 0-3 points. The total score ranges from 0-63. High scores indicate poor (dependent) health.

    Time frame: Baseline and 6th week

07

Study locations

1 of 1 sites recruiting
  • University of Health Sciences, Konya Beyhekim Training and Research Hospital, Department of Physical Medicine and Rehabilitation, Konya, Turkey 42060
    Konya, Konya 42080, Turkey (Türkiye)
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 25, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07261553
Lead sponsor
Konya Beyhekim Training and Research Hospital
Responsible party
Merve Albayrak (Dr., Konya Beyhekim Training and Research Hospital) — Principal investigator
First posted
Dec 3, 2025
Start date
Dec 30, 2024
Primary completion
Apr 1, 2026 (estimated)
Completion
May 15, 2026 (estimated)
Last update
Mar 25, 2026

Study contacts

Merve Albayrak, Dr
Contact
mervealbyrk20@gmail.com
+905556232674
ramazan Yılmaz, assoc prof
Contact
drramazanyilmaz@yahoo.com
Ramazan Yilmaz
study chair · Konya Beyhekim Training and Research Hospital

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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