- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07635927
Effect of Interest-Based Physical Training on Exercise Adherence
Effect of Interest-Based Physical Training on Exercise Adherence and Physical Fitness in College Students: The Mediating Role of Positive Affective Experience
This study aims to examine whether a physical training program designed based on individual interests can improve exercise adherence and physical fitness among college students, and to explore whether positive affective experience plays a mediating role in this process.
College student participants will be randomly assigned to either an interest-based physical training group or a control group (conventional physical education or no intervention). The interest-based training program includes personalized exercise activities such as team games, fitness challenges, and recreational sports, designed to enhance intrinsic motivation. The intervention will last for 12 weeks.
Primary outcome measures include exercise adherence (e.g., attendance rate, dropout rate) and physical fitness (e.g., cardiorespiratory endurance, muscular strength, flexibility). Secondary outcome measure is positive affective experience assessed by standardized questionnaires. Mediation analysis will be conducted to test whether the effect of interest-based training on adherence and fitness is mediated by positive affective experience.
The study has been approved by the Ethics Committee of the Academic Committee, Capital University of Physical Education and Sports (Approval Number:2025A055). All participants will provide informed consent before enrollment.
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Studientyp
Einschreibung (Tatsächlich)
Phase
- Unzutreffend
Kontakte und Standorte
Studienorte
-
-
Beijing Municipality
-
Beijing, Beijing Municipality, China, 100191
- Capital University of Physical Education and Sports
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Beschreibung
Inclusion Criteria:
Full-time college students aged 18-30 years
- Willing to participate and provide written informed consent
- Able to attend the scheduled physical training sessions (once per week, 90 minutes each)
- Physically capable of performing moderate-intensity physical training
Exclusion Criteria:
- - History of cardiovascular, cerebrovascular, or respiratory diseases (e.g., heart disease, asthma, hypertension)
- Musculoskeletal injuries or conditions that contraindicate exercise (e.g., fractures, severe arthritis, disc herniation)
- Current participation in another structured exercise or physical training program
- Use of medications that may affect heart rate or exercise tolerance (e.g., beta-blockers)
- Pregnancy or lactation
- Mental disorders or cognitive impairment that prevent understanding of the study procedures
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Sonstiges
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: Interest-Based Physical Training Group
Participants receive a 12-week physical training program designed based on individual interests, including team games, fitness challenges, and recreational sports, with sessions conducted 2-3 times per week.
|
A 12-week physical training program tailored to individual interests, including team games, fitness challenges, and recreational sports.
Sessions are conducted1 times per week, each lasting 90 minutes.
|
|
Aktiver Komparator: Regular Physical Training Group
Participants receive regular physical training sessions following the standard university curriculum, without individualized interest-based design.
|
Standard physical training sessions following the regular university curriculum, without individualized interest-based design.
Frequency and duration are matched to the experimental group.
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Exercise Adherence Questionnaire - Total Score
Zeitfenster: Baseline, 6 weeks, and 12 weeks (end of intervention)
|
A 14-item self-report questionnaire measuring exercise adherence across three dimensions: Behavioral Habits (items 1-4, 4 items), Effort Investment (items 5-9, 5 items), and Emotional Experience (items 10-14, 5 items).
Each item is rated on a 5-point Likert scale (1=strongly disagree to 5=strongly agree).
Total score ranges from 14 to 70, with higher scores indicating better exercise adherence.
|
Baseline, 6 weeks, and 12 weeks (end of intervention)
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Vital Capacity
Zeitfenster: Baseline and 12 weeks
|
Maximum amount of air exhaled after maximal inhalation, measured in milliliters using a spirometer.
Higher value indicates better respiratory function.
|
Baseline and 12 weeks
|
|
50-meter Sprint Time
Zeitfenster: Baseline and 12 weeks
|
Time in seconds to complete a 50-meter sprint.
Lower time indicates better speed.
|
Baseline and 12 weeks
|
|
Cardiorespiratory Endurance (800m run for females, 1000m run for males)
Zeitfenster: Baseline and 12 weeks
|
Time in minutes to complete the distance (800m for females, 1000m for males).
Lower time indicates better endurance.
|
Baseline and 12 weeks
|
|
Sit-and-Reach Test
Zeitfenster: Baseline and 12 weeks
|
Distance reached in centimeters while sitting and reaching forward.
Higher distance indicates better flexibility.
|
Baseline and 12 weeks
|
|
Standing Long Jump
Zeitfenster: Baseline and 12 weeks
|
Distance jumped in centimeters from a standing start.
Greater distance indicates better lower body explosive strength.
|
Baseline and 12 weeks
|
|
Pull-ups (males)
Zeitfenster: Baseline and 12 weeks
|
Number of pull-ups completed.
Higher number indicates better upper body muscular endurance.
|
Baseline and 12 weeks
|
|
Sit-ups (females)
Zeitfenster: Baseline and 12 weeks
|
Number of sit-ups completed in one minute.
Higher number indicates better abdominal muscular endurance.
|
Baseline and 12 weeks
|
Mitarbeiter und Ermittler
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Andere Studien-ID-Nummern
- 2025A055
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .
Klinische Studien zur Gesunde Freiwillige
-
3i SolutionsKGK Science Inc.Noch keine RekrutierungBioverfügbarkeit Heathy Volunteers | Pharmakokinetische ParameterKanada
-
Sarfez Pharmaceuticals, Inc.AbgeschlossenBioverfügbarkeit Heathy VolunteersVereinigte Staaten
-
Factors Group of Nutritional Companies Inc.IsuraAbgeschlossenSicherheit | Bioverfügbarkeit Heathy VolunteersKanada
-
Sarfez Pharmaceuticals, Inc.Abgeschlossen
-
Aziende Chimiche Riunite Angelini Francesco S.p.ASocraTec R&D GmbHAbgeschlossenBioverfügbarkeitsstudie | Bioverfügbarkeit Heathy Volunteers | BioäquivalenzDeutschland
-
National Research Council, SpainAktiv, nicht rekrutierendBioverfügbarkeit Heathy Volunteers | Bioverfügbarkeit und AUCSpanien
Klinische Studien zur Interest-Based Physical Training;
-
Keller Army Community HospitalBeendetSportliche Leistung | GewichthebenVereinigte Staaten
-
McGill UniversityCanadian Institutes of Health Research (CIHR)AbgeschlossenChronische Rückenschmerzen (CLBP)Kanada
-
Kansas State UniversityNational Development and Research Institutes, Inc.Abgeschlossen
-
University of MiamiUnited States Department of DefenseBeendet
-
University of ZurichRadboud University Medical Center; Johannes Gutenberg University Mainz; Leuven...Abgeschlossen
-
Wuhan Mental Health CentreNoch keine RekrutierungAufmerksamkeitsdefizit-Hyperaktivitätsstörung (ADHS)
-
Memorial Sloan Kettering Cancer CenterAktiv, nicht rekrutierendBrustkrebsVereinigte Staaten
-
King Edward Medical UniversityAbgeschlossenSchulpsychiatrische Ausbildung von LehrernPakistan
-
Hospital Universitario La PazInstituto de Investigación Hospital Universitario La PazRekrutierung
-
Necmettin Erbakan UniversityAbgeschlossenAkute Exazerbation von COPDTruthahn